Page last updated: 2024-12-04

trimethylenediamine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

trimethylenediamine: RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

trimethylenediamine : An alkane-alpha,omega-diamine comprising a propane skeleton with amino substituents at positions 1 and 3. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID428
CHEMBL ID174324
CHEBI ID15725
CHEBI ID35411
MeSH IDM0054214

Synonyms (87)

Synonym
wln: z3z
nsc8154
1,3-propylenediamine
nsc-8154
CHEBI:15725 ,
KBIO1_001458
DIVK1C_006514
SPECTRUM_001150
SPECTRUM4_001903
SPECTRUM5_000586
inchi=1/c3h10n2/c4-2-1-3-5/h1-5h
alpha,omega-propanediamine
einecs 203-702-7
ai3-25358
brn 0605277
nsc 8154
ccris 4054
1,3-propanediamine
109-76-2
trimethylenediamine
1,3-diaminopropane
C00986
propane-1,3-diamine
1,3-diaminopropane, >=99%
18773-03-0
KBIOSS_001630
KBIO2_001630
KBIO2_006766
KBIO2_004198
KBIOGR_002492
SPECPLUS_000418
NCGC00178092-01
B4A724BF-48DB-479D-B403-B44C7C956D5B
D0114
BMSE000001
CHEMBL174324
AKOS000119455
BMSE000872
ec 203-702-7
4-04-00-01258 (beilstein handbook reference)
unii-cb3isl56kg
cb3isl56kg ,
BMSE000796
68333-86-8
FT-0606614
1,3-diaminepropane
CHEBI:35411
1,3-propane-d6-diamine
3-aminopropylamine
.alpha.,.omega.-propanediamine
diaminopropane, 1,3-
BP-21144
BBL027701
J-503883
1, 3-diaminopropane
1,3 diaminopropane
1,3-diamino propane
1,3diaminopropane
1.3-diaminopropane
1,3 -diaminopropane
1,3-propane diamine
1,3-diamino-propane
h2n(ch2)3nh2
1,3-propandiamine
aminopropylamine
352438-78-9
mfcd00008228
DTXSID1021906
347840-13-5
F2191-0286
1,3-diaminopropan
a,w-propanediamine
1,3-diamino-n-propane
1,3-trimethylenediamine
Q161498
AMY21886
STL194260
HY-42210
CS-0020848
STR02314
1,3-diaminopropane dihydrobromide, >/=98%
propane-1,3-diammonium bromide
BP-26277
EN300-20409
1,3-propane-1,1,3,3-d4-diamine(9ci)
PD099153
Z104478068

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" A number of methods are used to reduce toxicity and improve the bioavailability of the fatty amine derivatives in these tests."( Improving ready biodegradability testing of fatty amine derivatives.
Galobardes, M; Gancet, C; Hirschen, M; Lemaire, P; Rosenblom, J; van Ginkel, CG, 2008
)
0.35
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
reagentA substance used in a chemical reaction to detect, measure, examine, or produce other substances.
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
alkane-alpha,omega-diamineA primary diamine that is ethane or a higher alkane in which a hydrogen of each of the terminal methyl groups has been replaced by an amino group. H2NCH2(CH2)nCH2NH2, where n = 0, 1, 2, etc.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (9)

PathwayProteinsCompounds
beta-Alanine Metabolism927
GABA-Transaminase Deficiency927
Ureidopropionase Deficiency927
Carnosinuria, Carnosinemia927
Metabolism of proteins1058144
Post-translational protein modification666112
Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation4626
Hypusinylation28
Beta-alanine biosynthesis I312

Bioassays (16)

Assay IDTitleYearJournalArticle
AID143007Percent [3H]MK-801 bound to N-methyl-D-aspartate glutamate receptor in the presence of 20 uM spermine assuming 100% in the absence of added diamine.1998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID25063Dissociation constant (pK2)1998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID448532Cytotoxicity against Mycobacterium bovis Bacillus Calmette-Guerin infected mouse J774 macrophage assessed as cell viability at 1 ug/mL after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID448381Cytotoxicity against mouse J774 macrophage assessed as cell viability at 1 ug/mL after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID143006Enhanced binding of [3H]MK-801 to N-methyl-D-aspartate glutamate receptor in presence of spermine1998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID15721Calculated partition coefficient (clogP)1998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID448531Cytotoxicity against mouse J774 macrophage assessed as cell viability at 100 ug/mL after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID1651238Drug metabolism in THF assessed as release of hydrogen disulphide at 5 mM in presence of S-acetylsulfanylethanethioate by DSP-3 probe based fluorescence assay2020Bioorganic & medicinal chemistry letters, 02-15, Volume: 30, Issue:4
Diacyl disulfides as the precursors for hydrogen persulfide (H
AID22299Partition coefficient (logP)1998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID25056Dissociation constant (pK1)1998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID448530Cytotoxicity against mouse J774 macrophage assessed as cell viability at 10 ug/mL after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID448380Antimicrobial activity against Mycobacterium tuberculosis H37Rv ATCC 27294 assessed as minimum inhibitory concentration after 24 hrs by micro plate Alamar blue assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID448534Cytotoxicity against Mycobacterium bovis Bacillus Calmette-Guerin infected mouse J774 macrophage assessed as cell viability at 100 ug/mL after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID15290Percentage of the diamine which is monoprotonated at pH 7.41998Journal of medicinal chemistry, Mar-12, Volume: 41, Issue:6
Molecular features associated with polyamine modulation of NMDA receptors.
AID448533Cytotoxicity against Mycobacterium bovis Bacillus Calmette-Guerin infected mouse J774 macrophage assessed as cell viability at 10 ug/mL after 48 hrs by MTT assay2009Bioorganic & medicinal chemistry letters, Sep-01, Volume: 19, Issue:17
Antitubercular activity of alpha,omega-diaminoalkanes, H2N(CH2)nNH2.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (160)

TimeframeStudies, This Drug (%)All Drugs %
pre-199058 (36.25)18.7374
1990's25 (15.63)18.2507
2000's29 (18.13)29.6817
2010's38 (23.75)24.3611
2020's10 (6.25)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.53

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index30.53 (24.57)
Research Supply Index5.09 (2.92)
Research Growth Index4.57 (4.65)
Search Engine Demand Index42.09 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.53)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (1.86%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other158 (98.14%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]