CID 9810930

Details

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Internal ID 9568b761-3f92-43d1-9996-755cf71dac44
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty amides > N-acyl amines
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C45H80N6O5/c1-3-38-24-16-17-28-44(56-38)35-37-26-27-39-41(45(29-21-23-36(2)55-45)49-43(48-44)51(37)39)42(53)54-34-20-14-12-10-8-6-4-5-7-9-11-13-15-25-40(52)50(33-22-31-47)32-19-18-30-46/h16,24,36-39,41H,3-15,17-23,25-35,46-47H2,1-2H3,(H,48,49)/t36-,37+,38+,39-,41-,44+,45-/m1/s1
InChI Key VTJKGZFFFMXPGP-COYUCOOOSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C45H80N6O5
Molecular Weight 785.20 g/mol
Exact Mass 784.61901967 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 7.85
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 9810930

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9550 95.50%
Caco-2 - 0.8429 84.29%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.6711 67.11%
OATP2B1 inhibitior - 0.5744 57.44%
OATP1B1 inhibitior + 0.8443 84.43%
OATP1B3 inhibitior + 0.9387 93.87%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9307 93.07%
P-glycoprotein inhibitior + 0.7427 74.27%
P-glycoprotein substrate + 0.7627 76.27%
CYP3A4 substrate + 0.7255 72.55%
CYP2C9 substrate - 0.8030 80.30%
CYP2D6 substrate - 0.8178 81.78%
CYP3A4 inhibition + 0.5804 58.04%
CYP2C9 inhibition - 0.8204 82.04%
CYP2C19 inhibition - 0.7664 76.64%
CYP2D6 inhibition - 0.8875 88.75%
CYP1A2 inhibition - 0.8196 81.96%
CYP2C8 inhibition + 0.6913 69.13%
CYP inhibitory promiscuity - 0.8986 89.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5687 56.87%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.9068 90.68%
Skin irritation - 0.7757 77.57%
Skin corrosion - 0.9124 91.24%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.5689 56.89%
skin sensitisation - 0.8470 84.70%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5736 57.36%
Acute Oral Toxicity (c) III 0.5897 58.97%
Estrogen receptor binding + 0.7664 76.64%
Androgen receptor binding + 0.7353 73.53%
Thyroid receptor binding + 0.5326 53.26%
Glucocorticoid receptor binding + 0.6358 63.58%
Aromatase binding + 0.6333 63.33%
PPAR gamma + 0.6557 65.57%
Honey bee toxicity - 0.7138 71.38%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.8800 88.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.69% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.29% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.65% 97.09%
CHEMBL202 P00374 Dihydrofolate reductase 96.30% 89.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.47% 94.45%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 90.68% 95.50%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.10% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 88.74% 100.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.69% 90.24%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.88% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.02% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.86% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.06% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 84.68% 92.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.72% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 81.24% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.60% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 9810930
LOTUS LTS0126688
wikiData Q105292774