Page last updated: 2024-11-08

bms 433771

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Description

BMS 433771: a fusion inhibitor of respiratory syncytial virus; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6478034
CHEMBL ID243876
SCHEMBL ID3822776
MeSH IDM0462051
PubMed CID500516
CHEMBL ID243875
MeSH IDM0462051

Synonyms (31)

Synonym
1-cyclopropyl-3-[[1-(4-hydroxybutyl)benzimidazol-2-yl]methyl]imidazo[4,5-c]pyridin-2-one
bms-433771
CHEMBL243876 ,
g2427554nw ,
unii-g2427554nw
543700-68-1
1-cyclopropyl-3-((1-(4-hydroxybutyl)-1h-benzimidazol-2-yl)methyl)-1,3-dihydroimidazo(4,5-c)pyridin-2-one
2h-imidazo(4,5-c)pyridin-2-one, 1-cyclopropyl-1,3-dihydro-3-((1-(4-hydroxybutyl)-1h-benzimidazol-2-yl)methyl)-
SCHEMBL3822776
1-cyclopropyl-3-[[1-(4-oxidanylbutyl)benzimidazol-2-yl]methyl]imidazo[4,5-c]pyridin-2-one
5no ,
bdbm50088178
DTXSID20202746
1-cyclopropyl-1,3-dihydro-3-[[1-(4-hydroxybutyl)-1h-benzimidazol-2-yl)methyl]-2h-imidazo[4,5-c]pyridin-2-one
1-cyclopropyl-3-((1-(4-hydroxybutyl)-1h-benzo[d]imidazol-2-yl)methyl)-1h-imidazo[4,5-c]pyridin-2(3h)-one
KSHJXDWYTZJUEI-UHFFFAOYSA-N
A857738
Q27278636
bms-433771 free base
543700-68-1 (free base)
CS-0078497
HY-120632
AKOS040748007
380603-10-1
CHEMBL243875
bms 433771
1-cyclopropyl-3-[[1-(3-hydroxypropyl)benzimidazol-2-yl]methyl]imidazo[4,5-c]pyridin-2-one
AKOS022175093
bms-433771 hcl hydrate
1-cyclopropyl-3-((1-(3-hydroxypropyl)-1h-benzo[d]imidazol-2-yl)methyl)-1h-imidazo[4,5-c]pyridin-2(3h)-one
DTXSID20191469

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
" These mt-QSARs offer also a good opportunity to construct drug-drug Complex Networks (CNs) that can be used to explore large and complex drug-viral species databases."( Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.
Chou, KC; González-Díaz, H; Martinez de la Vega, O; Prado-Prado, FJ; Ubeira, FM; Uriarte, E, 2009
)
0.35

Bioavailability

ExcerptReferenceRelevance
" 1-Cyclopropyl-1,3-dihydro-3-[[1-(4-hydroxybutyl)-1H-benzimidazol-2-yl]methyl]-2H-imidazo[4,5-c]pyridin-2-one (6m, BMS-433771) was identified as a potent RSV inhibitor demonstrating good bioavailability in the mouse, rat, dog and cynomolgus monkey that demonstrated antiviral activity in the BALB/c and cotton rat models of infection following oral administration."( Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
Cianci, CW; Civiello, RL; Clarke, J; Colonno, RJ; Combrink, KD; D'Arienzo, C; Dalterio, RA; Dando, S; Genovesi, EV; Gulgeze, HB; Kadow, KF; Krystal, M; Lamb, L; Li, Z; Marino, A; Meanwell, NA; Medina, I; Sin, N; Venables, BL; Wang, XA; Wright, JJ; Yang, Z; Yu, KL; Zadjura, L, 2007
)
0.34
", rat oral bioavailability of 89% for compound 17)."( The discovery of 1,2,3,9b-tetrahydro-5H-imidazo[2,1-a]isoindol-5-ones as a new class of respiratory syncytial virus (RSV) fusion inhibitors. Part 1.
Bond, S; Draffan, AG; Fenner, JE; Lambert, J; Lim, CY; Lin, B; Luttick, A; Mitchell, JP; Morton, CJ; Nearn, RH; Sanford, V; Stanislawski, PC; Tucker, SP, 2015
)
0.42
" This publication covers the medicinal chemistry efforts resulting in the identification of JNJ-53718678, an orally bioavailable RSV inhibitor that was shown to be efficacious in a phase 2a challenge study in healthy adult subjects and that is currently being evaluated in hospitalized infants and adults."( Discovery of 3-({5-Chloro-1-[3-(methylsulfonyl)propyl]-1
Battles, MB; Cooymans, L; Demin, S; Hu, L; Jonckers, THM; Koul, A; Kwanten, L; McLellan, JS; Raboisson, P; Roymans, D; Tahri, A; Van den Berg, J; Vendeville, S; Vos, A, 2020
)
0.56
"BMS-433771 is an orally bioavailable respiratory syncytial virus (RSV) inhibitor, functioning through inhibition of viral F protein-induced membrane fusion."( Antiviral activity and molecular mechanism of an orally active respiratory syncytial virus fusion inhibitor.
Cianci, C; Krystal, M; Meanwell, N, 2005
)
0.33
" 1-Cyclopropyl-1,3-dihydro-3-[[1-(4-hydroxybutyl)-1H-benzimidazol-2-yl]methyl]-2H-imidazo[4,5-c]pyridin-2-one (6m, BMS-433771) was identified as a potent RSV inhibitor demonstrating good bioavailability in the mouse, rat, dog and cynomolgus monkey that demonstrated antiviral activity in the BALB/c and cotton rat models of infection following oral administration."( Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
Cianci, CW; Civiello, RL; Clarke, J; Colonno, RJ; Combrink, KD; D'Arienzo, C; Dalterio, RA; Dando, S; Genovesi, EV; Gulgeze, HB; Kadow, KF; Krystal, M; Lamb, L; Li, Z; Marino, A; Meanwell, NA; Medina, I; Sin, N; Venables, BL; Wang, XA; Wright, JJ; Yang, Z; Yu, KL; Zadjura, L, 2007
)
0.34

Dosage Studied

ExcerptRelevanceReference
" By using the Long strain of RSV, prophylactic efficacy via oral dosing was observed in both animal models."( Oral efficacy of a respiratory syncytial virus inhibitor in rodent models of infection.
Cianci, C; Clark, J; Colonno, R; Combrink, K; D'Arienzo, C; Genovesi, EV; Krystal, M; Lamb, L; Li, Z; Meanwell, N; Medina, I; Sin, N; Yang, H; Yang, Z; Yu, KL; Zadjura, L, 2004
)
0.32
" BMS-433771 is also efficacious against RSV infection in two rodent models when dosed orally prior to infection."( Antiviral activity and molecular mechanism of an orally active respiratory syncytial virus fusion inhibitor.
Cianci, C; Krystal, M; Meanwell, N, 2005
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (7)

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Acetyl-CoA acetyltransferase, mitochondrialRattus norvegicus (Norway rat)EC50 (µMol)0.02800.02800.02800.0280AID1500737
Fusion glycoprotein F0 Human orthopneumovirusEC50 (µMol)0.01860.00010.01400.0280AID1350230; AID1500737; AID1660198
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Cytochrome P450 1A2Homo sapiens (human)INH28.00000.10000.10000.1000AID429288
Cytochrome P450 3A4Homo sapiens (human)INH28.00001.70002.85004.0000AID429287
Cytochrome P450 2D6Homo sapiens (human)INH28.00003.20003.40003.6000AID429286
Cytochrome P450 2C9 Homo sapiens (human)INH28.00004.40007.00009.1000AID429284
Acetyl-CoA acetyltransferase, mitochondrialRattus norvegicus (Norway rat)EC90 (µMol)0.42000.42000.42000.4200AID1500737
Cytochrome P450 2C19Homo sapiens (human)INH28.00007.00007.00007.0000AID429285
Fusion glycoprotein F0 Human orthopneumovirusEC90 (µMol)0.42000.42000.42000.4200AID1500737
[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 (86)

Assay IDTitleYearJournalArticle
AID736357Apparent permeability in dog RRCK cells2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID429287Inhibition of CYP3A42009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID736364Apparent intrinsic clearance in human liver microsomes2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID392535Antiviral activity against Sendai virus2009Bioorganic & medicinal chemistry, Jan-15, Volume: 17, Issue:2
Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.
AID293321Metabolic stability human liver microsomes2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID1500737Inhibition of Respiratory syncytial virus Long fusion glycoprotein infected in Hep2 cells assessed as reduction in virus-induced cytopathic effect after 4 days by spectrophotometric analysis2017European journal of medicinal chemistry, Sep-29, Volume: 138Discovery of methylsulfonyl indazoles as potent and orally active respiratory syncytial Virus(RSV) fusion inhibitors.
AID429281Antiviral activity against RSV assessed as inhibition of viral replication by cell based assay2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID293319Cytotoxicity against HEp2 cells2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID392513Antiviral activity against HIV12009Bioorganic & medicinal chemistry, Jan-15, Volume: 17, Issue:2
Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.
AID293322Permeability across human Caco-2 cells2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID429294Antiviral activity against RSV infected in BALB/c mouse assessed as log reduction in viral titer2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID1350239Oral bioavailability in Balb/c mouse at 10 mg/kg administered as single dose via gavage by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID308545Antiviral activity against RSV long A with F1 protein K394R mutation in HEp2 cells2007Bioorganic & medicinal chemistry letters, Aug-15, Volume: 17, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 5: Optimization of benzimidazole substitution patterns towards derivatives with improved activity.
AID1206974Solubility of the compound in phosphate buffer at pH 6.5 after overnight incubation by LYSA method2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID429284Inhibition of CYP2C92009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID293328Antiviral activity against RSV infected BALB/c mouse per lung at 50 mg/kg/day2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID736351Apparent intrinsic clearance in rat liver microsomes assessed per mg protein2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID429289Oral bioavailability in rat at 5 mg/kg2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID1660198Inhibition of GFP-fused RSV 224 fusion protein infected in human HeLa cells assessed as reduction in viral replication after 3 days by laser microscopic analysis2020Journal of medicinal chemistry, 08-13, Volume: 63, Issue:15
Discovery of 3-({5-Chloro-1-[3-(methylsulfonyl)propyl]-1
AID1206975Permeability of the compound at 150 uM by PAMPA2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID1350232Clearance in Balb/c mouse at 1 mg/kg, iv administered as single bolus dose by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID392534Antiviral activity against Poliovirus2009Bioorganic & medicinal chemistry, Jan-15, Volume: 17, Issue:2
Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.
AID583681Antiviral activity against respiratory syncytial virus long strain infected in cotton rat assessed as reduction in epithelial lining fluid viral load2010Antimicrobial agents and chemotherapy, Nov, Volume: 54, Issue:11
Pharmacokinetics-pharmacodynamics of a respiratory syncytial virus fusion inhibitor in the cotton rat model.
AID293320Therapeutic index, ratio of CC50 for HEp2 cells to EC50 for RSV Long2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID1350236Cmax in Balb/c mouse at 10 mg/kg, po administered as single dose via gavage by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID1206976Clearance in human liver microsomes at 1 uM2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID429283Permeability across human Caco-2 cells2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID368973Antiviral activity against RSV infected human Hep2 cells assessed as reduction of plaque formation pretreated 2 hrs before viral infection2007Antimicrobial agents and chemotherapy, Sep, Volume: 51, Issue:9
RSV604, a novel inhibitor of respiratory syncytial virus replication.
AID429295Antiviral activity against RSV infected in BALB/c mouse assessed as reduction viral replication by RT-PCR2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID429282Metabolic stability in human liver mocrosomes2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID293325AUC in dog at 0.5 mg/kg, po2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID293331Inhibition of cytochrome P4502007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID392523Antiviral activity against Human rhinovirus2009Bioorganic & medicinal chemistry, Jan-15, Volume: 17, Issue:2
Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.
AID1206972Antiviral activity against Respiratory syncytial virus A infected in human Hep2 cells assessed as reduction of virus-induced cytopathic effect after 6 days by CCK-8 assay2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID293330Antiviral activity against RSV infected cotton rat per lung at 50 mg/kg/day2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID1500738Cytotoxicity against human Hep2 cells after 4 days2017European journal of medicinal chemistry, Sep-29, Volume: 138Discovery of methylsulfonyl indazoles as potent and orally active respiratory syncytial Virus(RSV) fusion inhibitors.
AID368974Antiviral activity against RSV infected human Hep2 cells assessed as reduction of plaque formation treated 6 hrs after viral infection2007Antimicrobial agents and chemotherapy, Sep, Volume: 51, Issue:9
RSV604, a novel inhibitor of respiratory syncytial virus replication.
AID1206977Clearance in mouse liver microsomes at 1 uM2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID293332Partition coefficient, log P at pH 6.52007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID1350241Antiviral activity against human respiratory syncytial virus A2 infected in Balb/c mouse assessed as reduction in lung viral load at 50 mg/kg, po administered once daily pretreated for 1 hr on day 0 followed by viral infection and subsequent compound dosi2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID1350233Half life in Balb/c mouse at 1 mg/kg, iv administered as single bolus dose by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID1350238AUC (0 to infinity) in Balb/c mouse at 10 mg/kg, po administered as single dose via gavage by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID1190756Resistance index, ratio of EC50 for VP-14637 resistant respiratory syncytial virus Long expressing F protein D489Y mutant to EC50 for wild type Respiratory syncytial virus B12015Bioorganic & medicinal chemistry letters, Feb-15, Volume: 25, Issue:4
1,2,3,9b-Tetrahydro-5H-imidazo[2,1-a]isoindol-5-ones as a new class of respiratory syncytial virus (RSV) fusion inhibitors. Part 2: identification of BTA9881 as a preclinical candidate.
AID369150Antiviral activity against RSV infected human Hep2 cells assessed as plaque reduction treated concurrently with viral infection by plaque reduction assay2007Antimicrobial agents and chemotherapy, Sep, Volume: 51, Issue:9
RSV604, a novel inhibitor of respiratory syncytial virus replication.
AID583680Antiviral activity against respiratory syncytial virus long strain infected in po dosed cotton rat assessed as log reduction in viral load at 5000 ng/h/ml compound AUC2010Antimicrobial agents and chemotherapy, Nov, Volume: 54, Issue:11
Pharmacokinetics-pharmacodynamics of a respiratory syncytial virus fusion inhibitor in the cotton rat model.
AID736359Volume of distribution in steady state in rat2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID1206973Cytotoxicity against human Hep2 cells assessed as cell viability after 6 days by CCK-8 assay2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID1350234Volume of distribution in Balb/c mouse at 1 mg/kg, iv administered as single bolus dose by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID1206979Inhibition of CYP2C9 in human liver microsomes by LC-MS/MS analysis2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID429286Inhibition of CYP2D62009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID429285Inhibition of CYP2C192009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID1261339Antiviral activity against RSV2015Bioorganic & medicinal chemistry, Nov-01, Volume: 23, Issue:21
Antiviral activity of benzotriazole derivatives. 5-[4-(Benzotriazol-2-yl)phenoxy]-2,2-dimethylpentanoic acids potently and selectively inhibit Coxsackie Virus B5.
AID293318Antiviral activity against RSV Long in HEp2 cells assessed as reduction of virus-induced cytopathic effect2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID736358Half life in iv dosed rat2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID736362Apparent intrinsic clearance in human hepatocytes assessed per million cells2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID1190755Resistance index, ratio of EC50 for drug resistant respiratory syncytial virus Long expressing F protein Q494L mutant to EC50 for wild type Respiratory syncytial virus B12015Bioorganic & medicinal chemistry letters, Feb-15, Volume: 25, Issue:4
1,2,3,9b-Tetrahydro-5H-imidazo[2,1-a]isoindol-5-ones as a new class of respiratory syncytial virus (RSV) fusion inhibitors. Part 2: identification of BTA9881 as a preclinical candidate.
AID1190679Selectivity ratio of EC50 for Respiratory syncytial virus A Long harboring F protein T335I mutant infected in human Hep2 cells to EC50 for wild-type Respiratory syncytial virus A Long infected in human Hep2 cells2015Bioorganic & medicinal chemistry letters, Feb-15, Volume: 25, Issue:4
The discovery of 1,2,3,9b-tetrahydro-5H-imidazo[2,1-a]isoindol-5-ones as a new class of respiratory syncytial virus (RSV) fusion inhibitors. Part 1.
AID1206980Inhibition of CYP2D6 in human liver microsomes by LC-MS/MS analysis2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID293323AUC in mouse at 10 mg/kg, po2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID1206978Inhibition of CYP3A4 in human liver microsomes by LC-MS/MS analysis2015ACS medicinal chemistry letters, Mar-12, Volume: 6, Issue:3
Discovery of imidazopyridine derivatives as highly potent respiratory syncytial virus fusion inhibitors.
AID1350231Cytotoxicity against human Hep2 cells after 5 days by CCK8 assay2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID1350237Tmax in Balb/c mouse at 10 mg/kg, po administered as single dose via gavage by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID429292Volume of distribution at steady state in rat at 1 mg/kg, iv2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID1660200Selectivity index, ratio of CC50 for human HeLa cells to EC50 GFP-fused RSV 224 fusion protein infected in human HeLa cells2020Journal of medicinal chemistry, 08-13, Volume: 63, Issue:15
Discovery of 3-({5-Chloro-1-[3-(methylsulfonyl)propyl]-1
AID293326AUC in cynamologous monkey at 0.5 mg/kg, po2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID736360Oral bioavailability in rat2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID429288Inhibition of CYP1A22009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID429290Cmax in rat at 5 mg/kg, po2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID736350Apparent intrinsic clearance in human liver microsomes assessed per mg protein2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID429293Terminal half life in rat at 1 mg/kg, iv2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID1350230Inhibition of RSV long strain fusion protein infected in Hep2 cells assessed as reduction in virus-induced cytopathic effect after 5 days by CCK8 assay2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID736356Octanol-neutral buffer partition co-efficient, log D of the compound at pH 7.42013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID429291Total clearance in rat at 1 mg/kg, iv2009Bioorganic & medicinal chemistry letters, Aug-15, Volume: 19, Issue:16
Respiratory syncytial virus fusion inhibitors. Part 7: structure-activity relationships associated with a series of isatin oximes that demonstrate antiviral activity in vivo.
AID736361Intrinsic clearance in rat plasma2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID1660199Cytotoxicity against human HeLa cells assessed as reduction in cell viability after 3 days by ATPlite assay2020Journal of medicinal chemistry, 08-13, Volume: 63, Issue:15
Discovery of 3-({5-Chloro-1-[3-(methylsulfonyl)propyl]-1
AID1190754Resistance index, ratio of EC50 for drug resistant respiratory syncytial virus B1 expressing F protein L141F mutant to EC50 for wild type Respiratory syncytial virus B12015Bioorganic & medicinal chemistry letters, Feb-15, Volume: 25, Issue:4
1,2,3,9b-Tetrahydro-5H-imidazo[2,1-a]isoindol-5-ones as a new class of respiratory syncytial virus (RSV) fusion inhibitors. Part 2: identification of BTA9881 as a preclinical candidate.
AID392531Antiviral activity against influenza virus2009Bioorganic & medicinal chemistry, Jan-15, Volume: 17, Issue:2
Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.
AID293324AUC in rat at 5 mg/kg, po2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID736353Apparent intrinsic clearance in mouse liver microsomes assessed per mg protein2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID1350235AUC (0 to infinity) in Balb/c mouse at 1 mg/kg, iv administered as single bolus dose by LC-MS/MS analysis2018ACS medicinal chemistry letters, Feb-08, Volume: 9, Issue:2
Discovery of 3,3'-Spiro[Azetidine]-2-oxo-indoline Derivatives as Fusion Inhibitors for Treatment of RSV Infection.
AID736365Antiviral activity against Respiratory syncytial virus A2 infected in A549 cells after 3 days by CelltitreGlo assay2013Bioorganic & medicinal chemistry letters, Feb-01, Volume: 23, Issue:3
Non-benzimidazole containing inhibitors of respiratory syncytial virus.
AID293321Metabolic stability human liver microsomes2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID293322Permeability across human Caco-2 cells2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID293319Cytotoxicity against HEp2 cells2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID293320Therapeutic index, ratio of CC50 for HEp2 cells to EC50 for RSV Long2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
AID293318Antiviral activity against RSV Long in HEp2 cells assessed as reduction of virus-induced cytopathic effect2007Bioorganic & medicinal chemistry letters, Feb-15, Volume: 17, Issue:4
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (24)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's13 (54.17)29.6817
2010's10 (41.67)24.3611
2020's1 (4.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.68

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 Index11.68 (24.57)
Research Supply Index2.56 (2.92)
Research Growth Index4.25 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.68)

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%
Reviews3 (25.00%)6.00%
Case Studies0 (0.00%)4.05%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Observational0 (0.00%)0.25%
Other14 (100.00%)84.16%
Other9 (75.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]