Page last updated: 2024-11-11

mdl 73811

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Description

MDL 73811: structure given in first source; RN given refers to (Z)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6436013
CHEMBL ID381751
SCHEMBL ID952291
MeSH IDM0180928
PubMed CID14722762
CHEMBL ID4276912
SCHEMBL ID952295
SCHEMBL ID9054168
MeSH IDM0180928

Synonyms (26)

Synonym
5-{[(z)-4-aminobut-2-enyl](methylamino)}adenosine
(2r,3r,4s,5r)-2-(6-amino-9h-purin-9-yl)-5-(((4-aminobut-2-enyl)(methyl)amino)methyl)tetrahydrofuran-3,4-diol
bdbm50335525
(2r,3r,4s,5r)-2-(6-amino-9h-purin-9-yl)-5-((((z)-4-aminobut-2-enyl)(methyl)amino)methyl)tetrahydrofuran-3,4-diol
(2r,3r,4s,5r,z)-2-(6-amino-9h-purin-9-yl)-5-(((4-aminobut-2-enyl)(methyl)amino)methyl)-tetrahydrofuran-3,4-diol
123642-27-3
5'-(((z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine
abeado
adenosine, 5'-((4-amino-2-butenyl)methylamino)-5'-deoxy-, (z)-
mdl-73811
CHEMBL381751 ,
(2r,3s,4r,5r)-2-[[[(z)-4-aminobut-2-enyl]-methylamino]methyl]-5-(6-aminopurin-9-yl)oxolane-3,4-diol
7gi49jb39o ,
unii-7gi49jb39o
adenosine,5'-[[(2z)-4-amino-2-buten-1-yl]methylamino]-5'-deoxy-
adenosine, 5'-(((2z)-4-amino-2-buten-1-yl)methylamino)-5'-deoxy-
mdl73811
SCHEMBL952291
5'-{[(z)-4-amino-2-butenyl]methylamino}-5'-deoxyadenosine
Q27268253
mdl 73811
SCHEMBL952295
SCHEMBL9054168
128490-00-6
(2r,3s,4r,5r)-2-[[[(e)-4-aminobut-2-enyl]-methylamino]methyl]-5-(6-aminopurin-9-yl)oxolane-3,4-diol
CHEMBL4276912

Research Excerpts

Dosage Studied

5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (1, also known as MDL 73811, or AbeAdo) has curative efficacy at a low dosage in a hemolymphatic model of HAT. No demonstrable effect in a mouse model of the CNS stage due to poor blood-brain barrier permeation. Pharmacokinetic studies of mice following intraperitoneal dosing showed that the half-life of Genz-644131 was threefold greater than that of MDL73811.

Genz-644131 was threefold greater than that of MDL 73811 (7) The lead compound, 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (1) has curative efficacy at a low dosage in a hemolymphatic model of HAT.

ExcerptRelevanceReference
" Pharmacokinetic studies of mice following intraperitoneal dosing showed that the half-life of Genz-644131 was threefold greater than that of MDL 73811 (7."( Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
Bacchi, CJ; Barker, RH; Celatka, CA; Fitzpatrick, R; Hirth, B; Kaiser, M; Klinger, JD; Liu, H; Phillips, MA; Rodriguez, A; Sybertz, E; Willert, EK; Xiang, Y; Yarlett, N, 2009
)
0.55
" The lead compound, 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (1, also known as MDL 73811, or AbeAdo), has curative efficacy at a low dosage in a hemolymphatic model of HAT but displayed no demonstrable effect in a mouse model of the CNS stage of HAT due to poor blood-brain barrier permeation."( Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
Brockway, AJ; Cosner, CC; De Brabander, JK; MacMillan, KS; Peel, M; Phillips, MA; Richardson, TE; Volkov, OA; Wring, SA, 2017
)
0.89
" Pharmacokinetic studies of mice following intraperitoneal dosing showed that the half-life of Genz-644131 was threefold greater than that of MDL 73811 (7."( Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
Bacchi, CJ; Barker, RH; Celatka, CA; Fitzpatrick, R; Hirth, B; Kaiser, M; Klinger, JD; Liu, H; Phillips, MA; Rodriguez, A; Sybertz, E; Willert, EK; Xiang, Y; Yarlett, N, 2009
)
0.35
" The lead compound, 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (1, also known as MDL 73811, or AbeAdo), has curative efficacy at a low dosage in a hemolymphatic model of HAT but displayed no demonstrable effect in a mouse model of the CNS stage of HAT due to poor blood-brain barrier permeation."( Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
Brockway, AJ; Cosner, CC; De Brabander, JK; MacMillan, KS; Peel, M; Phillips, MA; Richardson, TE; Volkov, OA; Wring, SA, 2017
)
0.46
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (5)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Cytochrome P450 1A2Homo sapiens (human)IC50 (µMol)5.00000.00011.774010.0000AID562011
Cytochrome P450 3A4Homo sapiens (human)IC50 (µMol)5.00000.00011.753610.0000AID562007
Cytochrome P450 2D6Homo sapiens (human)IC50 (µMol)5.00000.00002.015110.0000AID562008
Cytochrome P450 2C9 Homo sapiens (human)IC50 (µMol)5.00000.00002.800510.0000AID562009
Cytochrome P450 2C19Homo sapiens (human)IC50 (µMol)5.00000.00002.398310.0000AID562010
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (42)

Processvia Protein(s)Taxonomy
steroid catabolic processCytochrome P450 1A2Homo sapiens (human)
porphyrin-containing compound metabolic processCytochrome P450 1A2Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 1A2Homo sapiens (human)
cholesterol metabolic processCytochrome P450 1A2Homo sapiens (human)
estrogen metabolic processCytochrome P450 1A2Homo sapiens (human)
toxin biosynthetic processCytochrome P450 1A2Homo sapiens (human)
post-embryonic developmentCytochrome P450 1A2Homo sapiens (human)
alkaloid metabolic processCytochrome P450 1A2Homo sapiens (human)
regulation of gene expressionCytochrome P450 1A2Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 1A2Homo sapiens (human)
dibenzo-p-dioxin metabolic processCytochrome P450 1A2Homo sapiens (human)
epoxygenase P450 pathwayCytochrome P450 1A2Homo sapiens (human)
lung developmentCytochrome P450 1A2Homo sapiens (human)
methylationCytochrome P450 1A2Homo sapiens (human)
monocarboxylic acid metabolic processCytochrome P450 1A2Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 1A2Homo sapiens (human)
retinol metabolic processCytochrome P450 1A2Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 1A2Homo sapiens (human)
cellular respirationCytochrome P450 1A2Homo sapiens (human)
aflatoxin metabolic processCytochrome P450 1A2Homo sapiens (human)
hydrogen peroxide biosynthetic processCytochrome P450 1A2Homo sapiens (human)
oxidative demethylationCytochrome P450 1A2Homo sapiens (human)
cellular response to cadmium ionCytochrome P450 1A2Homo sapiens (human)
omega-hydroxylase P450 pathwayCytochrome P450 1A2Homo sapiens (human)
lipid hydroxylationCytochrome P450 3A4Homo sapiens (human)
lipid metabolic processCytochrome P450 3A4Homo sapiens (human)
steroid catabolic processCytochrome P450 3A4Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 3A4Homo sapiens (human)
steroid metabolic processCytochrome P450 3A4Homo sapiens (human)
cholesterol metabolic processCytochrome P450 3A4Homo sapiens (human)
androgen metabolic processCytochrome P450 3A4Homo sapiens (human)
estrogen metabolic processCytochrome P450 3A4Homo sapiens (human)
alkaloid catabolic processCytochrome P450 3A4Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 3A4Homo sapiens (human)
calcitriol biosynthetic process from calciolCytochrome P450 3A4Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 3A4Homo sapiens (human)
vitamin D metabolic processCytochrome P450 3A4Homo sapiens (human)
vitamin D catabolic processCytochrome P450 3A4Homo sapiens (human)
retinol metabolic processCytochrome P450 3A4Homo sapiens (human)
retinoic acid metabolic processCytochrome P450 3A4Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 3A4Homo sapiens (human)
aflatoxin metabolic processCytochrome P450 3A4Homo sapiens (human)
oxidative demethylationCytochrome P450 3A4Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 2D6Homo sapiens (human)
steroid metabolic processCytochrome P450 2D6Homo sapiens (human)
cholesterol metabolic processCytochrome P450 2D6Homo sapiens (human)
estrogen metabolic processCytochrome P450 2D6Homo sapiens (human)
coumarin metabolic processCytochrome P450 2D6Homo sapiens (human)
alkaloid metabolic processCytochrome P450 2D6Homo sapiens (human)
alkaloid catabolic processCytochrome P450 2D6Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 2D6Homo sapiens (human)
isoquinoline alkaloid metabolic processCytochrome P450 2D6Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 2D6Homo sapiens (human)
retinol metabolic processCytochrome P450 2D6Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 2D6Homo sapiens (human)
negative regulation of bindingCytochrome P450 2D6Homo sapiens (human)
oxidative demethylationCytochrome P450 2D6Homo sapiens (human)
negative regulation of cellular organofluorine metabolic processCytochrome P450 2D6Homo sapiens (human)
arachidonic acid metabolic processCytochrome P450 2D6Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 2C9 Homo sapiens (human)
steroid metabolic processCytochrome P450 2C9 Homo sapiens (human)
cholesterol metabolic processCytochrome P450 2C9 Homo sapiens (human)
estrogen metabolic processCytochrome P450 2C9 Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 2C9 Homo sapiens (human)
epoxygenase P450 pathwayCytochrome P450 2C9 Homo sapiens (human)
urea metabolic processCytochrome P450 2C9 Homo sapiens (human)
monocarboxylic acid metabolic processCytochrome P450 2C9 Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 2C9 Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 2C9 Homo sapiens (human)
amide metabolic processCytochrome P450 2C9 Homo sapiens (human)
icosanoid biosynthetic processCytochrome P450 2C9 Homo sapiens (human)
oxidative demethylationCytochrome P450 2C9 Homo sapiens (human)
omega-hydroxylase P450 pathwayCytochrome P450 2C9 Homo sapiens (human)
long-chain fatty acid metabolic processCytochrome P450 2C19Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 2C19Homo sapiens (human)
steroid metabolic processCytochrome P450 2C19Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 2C19Homo sapiens (human)
epoxygenase P450 pathwayCytochrome P450 2C19Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 2C19Homo sapiens (human)
omega-hydroxylase P450 pathwayCytochrome P450 2C19Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (34)

Processvia Protein(s)Taxonomy
monooxygenase activityCytochrome P450 1A2Homo sapiens (human)
iron ion bindingCytochrome P450 1A2Homo sapiens (human)
protein bindingCytochrome P450 1A2Homo sapiens (human)
electron transfer activityCytochrome P450 1A2Homo sapiens (human)
oxidoreductase activityCytochrome P450 1A2Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 1A2Homo sapiens (human)
enzyme bindingCytochrome P450 1A2Homo sapiens (human)
heme bindingCytochrome P450 1A2Homo sapiens (human)
demethylase activityCytochrome P450 1A2Homo sapiens (human)
caffeine oxidase activityCytochrome P450 1A2Homo sapiens (human)
aromatase activityCytochrome P450 1A2Homo sapiens (human)
estrogen 16-alpha-hydroxylase activityCytochrome P450 1A2Homo sapiens (human)
estrogen 2-hydroxylase activityCytochrome P450 1A2Homo sapiens (human)
hydroperoxy icosatetraenoate dehydratase activityCytochrome P450 1A2Homo sapiens (human)
monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
steroid bindingCytochrome P450 3A4Homo sapiens (human)
iron ion bindingCytochrome P450 3A4Homo sapiens (human)
protein bindingCytochrome P450 3A4Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
retinoic acid 4-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
oxidoreductase activityCytochrome P450 3A4Homo sapiens (human)
oxygen bindingCytochrome P450 3A4Homo sapiens (human)
enzyme bindingCytochrome P450 3A4Homo sapiens (human)
heme bindingCytochrome P450 3A4Homo sapiens (human)
vitamin D3 25-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
caffeine oxidase activityCytochrome P450 3A4Homo sapiens (human)
quinine 3-monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
testosterone 6-beta-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
1-alpha,25-dihydroxyvitamin D3 23-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 8,9 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 11,12 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 14,15 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
aromatase activityCytochrome P450 3A4Homo sapiens (human)
vitamin D 24-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
estrogen 16-alpha-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
estrogen 2-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
1,8-cineole 2-exo-monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
monooxygenase activityCytochrome P450 2D6Homo sapiens (human)
iron ion bindingCytochrome P450 2D6Homo sapiens (human)
oxidoreductase activityCytochrome P450 2D6Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 2D6Homo sapiens (human)
heme bindingCytochrome P450 2D6Homo sapiens (human)
anandamide 8,9 epoxidase activityCytochrome P450 2D6Homo sapiens (human)
anandamide 11,12 epoxidase activityCytochrome P450 2D6Homo sapiens (human)
anandamide 14,15 epoxidase activityCytochrome P450 2D6Homo sapiens (human)
monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
iron ion bindingCytochrome P450 2C9 Homo sapiens (human)
arachidonic acid epoxygenase activityCytochrome P450 2C9 Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 2C9 Homo sapiens (human)
arachidonic acid 14,15-epoxygenase activityCytochrome P450 2C9 Homo sapiens (human)
arachidonic acid 11,12-epoxygenase activityCytochrome P450 2C9 Homo sapiens (human)
oxidoreductase activityCytochrome P450 2C9 Homo sapiens (human)
(S)-limonene 6-monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
(S)-limonene 7-monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
caffeine oxidase activityCytochrome P450 2C9 Homo sapiens (human)
(R)-limonene 6-monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
aromatase activityCytochrome P450 2C9 Homo sapiens (human)
heme bindingCytochrome P450 2C9 Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 2C9 Homo sapiens (human)
monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
iron ion bindingCytochrome P450 2C19Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 2C19Homo sapiens (human)
oxidoreductase activityCytochrome P450 2C19Homo sapiens (human)
(S)-limonene 6-monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
(S)-limonene 7-monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
oxygen bindingCytochrome P450 2C19Homo sapiens (human)
enzyme bindingCytochrome P450 2C19Homo sapiens (human)
heme bindingCytochrome P450 2C19Homo sapiens (human)
(R)-limonene 6-monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
aromatase activityCytochrome P450 2C19Homo sapiens (human)
long-chain fatty acid omega-1 hydroxylase activityCytochrome P450 2C19Homo sapiens (human)
arachidonic acid epoxygenase activityCytochrome P450 2C19Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 2C19Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (6)

Processvia Protein(s)Taxonomy
endoplasmic reticulum membraneCytochrome P450 1A2Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 1A2Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 1A2Homo sapiens (human)
cytoplasmCytochrome P450 3A4Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 3A4Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 3A4Homo sapiens (human)
mitochondrionCytochrome P450 2D6Homo sapiens (human)
endoplasmic reticulumCytochrome P450 2D6Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 2D6Homo sapiens (human)
cytoplasmCytochrome P450 2D6Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2D6Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 2C9 Homo sapiens (human)
plasma membraneCytochrome P450 2C9 Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C9 Homo sapiens (human)
cytoplasmCytochrome P450 2C9 Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C9 Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 2C19Homo sapiens (human)
plasma membraneCytochrome P450 2C19Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C19Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C19Homo sapiens (human)
cytoplasmCytochrome P450 2C19Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (90)

Assay IDTitleYearJournalArticle
AID562013Protein binding in mouse plasma at pH 7.4 after 4 hrs2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562007Inhibition of human cytochrome P450 3A42009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID88931In vitro Neoplastic Anti Activity in Human Colon adenocarcinoma HT-29 Cell lines2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID214473In vitro antitrypanosomal activity against Trypanosomal 110 (EATRO)strain2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID562032Cmax in mouse brain at 50 mg/kg, ip administered as single dose2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID214483In vitro antitrypanosomal activity against Trypanosomal 269 (KETRI)strain2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID562015Metabolic stability in human assessed as compound remaining plasma after 4 hrs2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1463515Half life in mouse pooled liver microsomes at 1 uM in presence of NADPH by LC/MS/MS method2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID94406In vitro inhibition of of AdoMetDC derived from L1210 Murine Leukemia Cells.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID123039Ratio of number of mice cured to that of total treated with the compound at 50 mg/kg for 7 days2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID562017Permeability across basolateral to apical side of human Caco2 cells2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562036Antiparasitic activity against Trypanosoma brucei brucei LAB 110 EATRO infected in mouse assessed as mean survival days at 50 mg/kg/day, ip bid for 7 days administered on 1st day of infection and measured through day 40 post infection2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID561999Ratio of Kinact to Kiapp for Trypanosoma brucei AdoMetDC expressed in Escherichia coli2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID88844In vitro Antineoplastic Activity against Human non small cell lung carcinoma A549 Cell lines2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID559246Trypanocidal activity against Trypanosoma brucei brucei EATRO after 48 hrs2009Antimicrobial agents and chemotherapy, Aug, Volume: 53, Issue:8
Trypanocidal activity of 8-methyl-5'-{[(Z)-4-aminobut-2-enyl]-(methylamino)}adenosine (Genz-644131), an adenosylmethionine decarboxylase inhibitor.
AID562008Inhibition of human cytochrome P450 2D62009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562033Antiparasitic activity against Trypanosoma brucei brucei STIB 795 infected in mouse assessed as mean survival days at 50 mg/kg, ip qd for 4 days administered on 3rd day of infection (Rvb = 6.75 days)2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1463514Half life in human pooled liver microsomes at 1 uM in presence of NADPH by LC/MS/MS method2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID1463507Ratio of drug level in brain to blood in mouse at 10 mg/kg, iv or po after 15 mins to 24 hrs by LC/MS/MS method relative to control2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID233235Differential selectivity as the ratio of TC50 value to that of EC50 value.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID214477In vitro antitrypanosomal activity against Trypanosomal 243 (KETRI)strain2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID208078Mean survival days against T.b. rhodesiense KETRI 243 tested in mice after intra peritoneal administration at 25 mg/kg for 7 days.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID88774In vitro Antineoplastic Activity against Adriamycin resistant Human Breast adenocarcinoma MCF7-Adr Cell lines2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID279551Antiproliferative activity against Leishmania donovani DI700 promastigotes in presence of 100 uM spermidine2007Antimicrobial agents and chemotherapy, Feb, Volume: 51, Issue:2
Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.
AID562012Protein binding in human plasma at pH 7.4 after 4 hrs2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID352513Cmax in brain of single dose ip administered mouse2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID559249Ratio of Kinact to Kiapp for Trypanosoma brucei rhodesiense AdoMetDC2009Antimicrobial agents and chemotherapy, Aug, Volume: 53, Issue:8
Trypanocidal activity of 8-methyl-5'-{[(Z)-4-aminobut-2-enyl]-(methylamino)}adenosine (Genz-644131), an adenosylmethionine decarboxylase inhibitor.
AID214481In vitro antitrypanosomal activity against Trypanosomal 243 As 10e-3 (KETRI)strain2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID352505Inhibition of Trypanosoma brucei AdoMetDC assessed as ratio of Kinact to Ki(apparent)2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID279549Antiproliferative activity against Leishmania donovani DI700 promastigotes overproducing ADOMETDC enzyme2007Antimicrobial agents and chemotherapy, Feb, Volume: 51, Issue:2
Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.
AID559248Trypanocidal activity against Trypanosoma brucei rhodesiense KETRI2538 after 48 hrs2009Antimicrobial agents and chemotherapy, Aug, Volume: 53, Issue:8
Trypanocidal activity of 8-methyl-5'-{[(Z)-4-aminobut-2-enyl]-(methylamino)}adenosine (Genz-644131), an adenosylmethionine decarboxylase inhibitor.
AID261568Antitrypanosomal activity against Trypanosoma brucei2006Journal of medicinal chemistry, Mar-23, Volume: 49, Issue:6
Antitrypanosomal activity of 5'-deoxy-5'-(iodomethylene)adenosine and related 6-N-cyclopropyladenosine analogues.
AID208073Mean survival days against T.b. peritoneal administration at 50 mg/kg for 3 days.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID208072Mean survival days against T.b. peritoneal administration at 25 mg/kg for 3 days.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID562006Metabolic stability in human hepatocytes assessed as intrinsic clearance up to 45 mins by LC/MS/MS analysis2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562016Permeability across apical to basolateral side of human Caco2 cells2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562009Inhibition of human cytochrome P450 2C92009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID123034Ratio of number of mice cured to that of total treated with the compound at 100 mg/kg for 7 days2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID89009In vitro Antineoplastic Activity against Human ovarian carcinoma A121 Cell lines2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID352512Cmax in blood of single dose ip administered mouse2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID562001Kinetic solubility in dimethyl sulfoxide at pH 7.4 after 16 to 24 hrs by UV spectrophotometry2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID352510AUC in brain of single dose ip administered mouse2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID123037Ratio of number of mice cured to that of total treated with the compound at 25 mg/kg for 7 days2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID208077Mean survival days against T.b. rhodesiense KETRI 243 tested in mice after intra peritoneal administration at 100 mg/kg for 7 days.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID81441In Vitro Anti-HIV activity of the compound2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID208071Mean survival days against T.b. peritoneal administration at 10 mg/kg for 3 days.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID279548Antiproliferative activity against Leishmania donovani DI700 promastigotes overproducing SPDSYN enzyme2007Antimicrobial agents and chemotherapy, Feb, Volume: 51, Issue:2
Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.
AID562035Antiparasitic activity against Trypanosoma brucei brucei LAB 110 EATRO infected in mouse assessed as mean survival days at 50 mg/kg/day, ip bid for 4 days administered on 1st day of infection and measured through day 40 post infection2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562004Metabolic stability in human liver microsomes assessed as intrinsic clearance up to 45 mins by LC/MS/MS analysis2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1463511Antitrypanosomal activity against Trypanosoma brucei Lister 427 bloodstream forms assessed as inhibition of parasite growth incubated for 48 hrs by ATP-bioluminescence cell viability assay2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID562039Partition coefficient in RBCs2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562014Metabolic stability in rat plasma assessed as compound remaining after 4 hrs2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562029Half life in mouse at 50 mg/kg, ip administered as single dose2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID352509Half life in single dose ip administered mouse2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID352507Antitrypanosomal activity against Trypanosoma brucei brucei2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID123036Ratio of number of mice cured to that of total treated with the compound at 25 mg/kg for 3 days2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID559247Trypanocidal activity against Trypanosoma brucei rhodesiense KETRI243 after 48 hrs2009Antimicrobial agents and chemotherapy, Aug, Volume: 53, Issue:8
Trypanocidal activity of 8-methyl-5'-{[(Z)-4-aminobut-2-enyl]-(methylamino)}adenosine (Genz-644131), an adenosylmethionine decarboxylase inhibitor.
AID1463506Antitrypanosomal activity against Trypanosoma brucei brucei2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID562002Permeability of the compound after 4 hrs by PAMPA assay2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID352508AUC in blood of single dose ip administered mouse2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID562028AUC in mouse brain at 50 mg/kg, ip administered as single dose2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID561998Antiparasitic activity against Trypanosoma brucei rhodesiense STIB 900 clone after 72 hrs by Alamar blue assay2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID279550Antiproliferative activity against Leishmania donovani DI700 promastigotes in presence of 100 uM putrescine2007Antimicrobial agents and chemotherapy, Feb, Volume: 51, Issue:2
Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.
AID279547Antiproliferative activity against Leishmania donovani DI700 promastigotes overproducing ODC enzyme2007Antimicrobial agents and chemotherapy, Feb, Volume: 51, Issue:2
Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.
AID279546Antiproliferative activity against Leishmania donovani DI700 promastigotes2007Antimicrobial agents and chemotherapy, Feb, Volume: 51, Issue:2
Leishmania donovani polyamine biosynthetic enzyme overproducers as tools to investigate the mode of action of cytotoxic polyamine analogs.
AID352506Antitrypanosomal activity against Trypanosoma brucei rhodesiense2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID46624Concentration that causes morphological changes in noninfected CEM-SS cells2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID352515Distribution coefficient, log D at pH 7.4 by shake flask method2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID562010Inhibition of human cytochrome P450 2C192009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1463509Inhibition of Trypanosoma brucei AdoMetDC without pre-incubation for 30 mins before AdoMet substrate addition by RapidFire-mass spectrometry2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID562030Ratio of AUC in brain to blood for mouse at 50 mg/kg, ip administered as single dose2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562038Metabolic stability in rat whole blood assessed as compound remaining2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1463505Inhibition of His-tagged Trypanosoma brucei AdoMetDC expressed in Escherichia coli pre-incubated for 1 to 22 mins before AdoMet substrate addition2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID562042Antiparasitic activity against Trypanosoma brucei brucei LAB 110 EATRO infected in mouse assessed as parasitemia cure incidence at 50 mg/kg/day, ip bid for 4 days administered on 1st day of infection and measured through day 40 post infection2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562011Inhibition of human cytochrome P450 1A22009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID352514Antitrypanosomal activity against Trypanosoma brucei brucei infected mouse assessed as reduction in parasitemia2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID352511Ratio of AUC in brain to blood in single dose ip administered mouse2009Bioorganic & medicinal chemistry letters, Jun-01, Volume: 19, Issue:11
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).
AID1463513Apparent permeability in MDCK2-MDR1 cells at 3 uM incubated for 1 hr in presence of P-glycoprotein inhibitor GF120918 by LC/MS/MS method2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID562000Ratio of Kinact to Kiapp for human AdoMetDC expressed in Escherichia coli2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562031Cmax in mouse blood at 50 mg/kg, ip administered as single dose2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID562005Metabolic stability in rat hepatocytes assessed as intrinsic clearance up to 45 mins by LC/MS/MS analysis2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID123038Ratio of number of mice cured to that of total treated with the compound at 50 mg/kg for 3 days2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID208079Mean survival days against T.b. rhodesiense KETRI 243 tested in mice after intra peritoneal administration at 50 mg/kg for 7 days.2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID123035Ratio of number of mice cured to that of total treated with the compound at 10 mg/kg for 3 days2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID88777In vitro Neoplastic Anti Activity against Human Breast adenocarcinoma MCF-7 Cell lines2002Journal of medicinal chemistry, Nov-07, Volume: 45, Issue:23
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.
AID562027AUC in mouse blood at 50 mg/kg, ip administered as single dose2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1463504Inhibition of Trypanosoma brucei AdoMetDC pre-incubated for 30 mins before AdoMet substrate addition by RapidFire-mass spectrometry2017Bioorganic & medicinal chemistry, 10-15, Volume: 25, Issue:20
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.
AID562003Metabolic stability in rat liver microsomes assessed as intrinsic clearance up to 45 mins by LC/MS/MS analysis2009Antimicrobial agents and chemotherapy, May, Volume: 53, Issue:5
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.
AID1413032Growth inhibition of Plasmodium falciparum ITG2 infected in human erythrocytes assessed as reduction in [3H]-isoleucine incorporation pretreated for 24 hrs followed by [3H]-isoleucine addition and measured after 18 hrs by liquid scintillation counting met2018MedChemComm, Jul-01, Volume: 9, Issue:7
Synthesis and antiplasmodial activity of purine-based
AID1413031Growth inhibition of Plasmodium falciparum D6 infected in human erythrocytes assessed as reduction in [3H]-isoleucine incorporation pretreated for 24 hrs followed by [3H]-isoleucine addition and measured after 18 hrs by liquid scintillation counting metho2018MedChemComm, Jul-01, Volume: 9, Issue:7
Synthesis and antiplasmodial activity of purine-based
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (35)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's23 (65.71)18.2507
2000's10 (28.57)29.6817
2010's2 (5.71)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.19

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.19 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.27 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.19)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Reviews1 (2.94%)6.00%
Case Studies0 (0.00%)4.05%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Observational0 (0.00%)0.25%
Other7 (100.00%)84.16%
Other33 (97.06%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]