N-(2-methylpropyl)tridec-7-en-10,12-diynamide

Details

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Internal ID 94d33e3b-1007-41e1-ac66-8d89d964a804
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty amides > N-acyl amines
IUPAC Name N-(2-methylpropyl)tridec-7-en-10,12-diynamide
SMILES (Canonical) CC(C)CNC(=O)CCCCCC=CCC#CC#C
SMILES (Isomeric) CC(C)CNC(=O)CCCCCC=CCC#CC#C
InChI InChI=1S/C17H25NO/c1-4-5-6-7-8-9-10-11-12-13-14-17(19)18-15-16(2)3/h1,8-9,16H,7,10-15H2,2-3H3,(H,18,19)
InChI Key HCEUPTTYCDQZJN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H25NO
Molecular Weight 259.40 g/mol
Exact Mass 259.193614421 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(2-methylpropyl)tridec-7-en-10,12-diynamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.5627 56.27%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.4664 46.64%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.8746 87.46%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.7181 71.81%
P-glycoprotein inhibitior - 0.8569 85.69%
P-glycoprotein substrate - 0.7376 73.76%
CYP3A4 substrate + 0.5051 50.51%
CYP2C9 substrate + 0.6079 60.79%
CYP2D6 substrate - 0.8548 85.48%
CYP3A4 inhibition - 0.9132 91.32%
CYP2C9 inhibition - 0.8178 81.78%
CYP2C19 inhibition - 0.8526 85.26%
CYP2D6 inhibition - 0.9129 91.29%
CYP1A2 inhibition - 0.6959 69.59%
CYP2C8 inhibition - 0.8382 83.82%
CYP inhibitory promiscuity - 0.7369 73.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.6617 66.17%
Eye corrosion - 0.7593 75.93%
Eye irritation - 0.9536 95.36%
Skin irritation - 0.8041 80.41%
Skin corrosion - 0.9300 93.00%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3791 37.91%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.6038 60.38%
skin sensitisation - 0.8759 87.59%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7994 79.94%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6781 67.81%
Acute Oral Toxicity (c) III 0.7155 71.55%
Estrogen receptor binding - 0.6392 63.92%
Androgen receptor binding - 0.9006 90.06%
Thyroid receptor binding + 0.6384 63.84%
Glucocorticoid receptor binding - 0.5902 59.02%
Aromatase binding - 0.6144 61.44%
PPAR gamma + 0.6344 63.44%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6824 68.24%
Fish aquatic toxicity - 0.4578 45.78%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL230 P35354 Cyclooxygenase-2 98.03% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.96% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.61% 98.95%
CHEMBL4179 P45984 c-Jun N-terminal kinase 2 93.02% 90.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.01% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.93% 97.29%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 89.29% 96.67%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.25% 89.34%
CHEMBL221 P23219 Cyclooxygenase-1 88.59% 90.17%
CHEMBL2637 P53779 c-Jun N-terminal kinase 3 88.54% 92.75%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 88.54% 89.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.64% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.26% 96.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.20% 96.47%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.18% 85.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.02% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.89% 97.21%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.83% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 84.64% 94.73%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 84.26% 95.71%
CHEMBL1255126 O15151 Protein Mdm4 83.04% 90.20%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.20% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Blainvillea acmella

Cross-Links

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PubChem 85649031
LOTUS LTS0066570
wikiData Q105025647