CID 162981415

Details

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Internal ID a57f1cfd-97c5-4837-b734-d9f129c7f414
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H50N2O/c1-9-10-20-25(6)15-19(30)22(18(2)29(7)8)24(25,5)13-14-27(20)17-26(27)12-11-21(28)23(3,4)16-26/h18-22,30H,9-17,28H2,1-8H3/t18-,19+,20-,21-,22-,24-,25-,26-,27-/m0/s1
InChI Key UVVUDBUSZSDPJI-RUERYLGASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H50N2O
Molecular Weight 418.70 g/mol
Exact Mass 418.392314223 g/mol
Topological Polar Surface Area (TPSA) 49.50 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.45
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162981415

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 - 0.5461 54.61%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.7189 71.89%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.8941 89.41%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.5118 51.18%
P-glycoprotein inhibitior - 0.7784 77.84%
P-glycoprotein substrate + 0.5213 52.13%
CYP3A4 substrate + 0.6348 63.48%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate + 0.5352 53.52%
CYP3A4 inhibition - 0.5396 53.96%
CYP2C9 inhibition - 0.7280 72.80%
CYP2C19 inhibition - 0.8226 82.26%
CYP2D6 inhibition - 0.7709 77.09%
CYP1A2 inhibition - 0.7704 77.04%
CYP2C8 inhibition - 0.7195 71.95%
CYP inhibitory promiscuity - 0.6480 64.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5767 57.67%
Eye corrosion - 0.9725 97.25%
Eye irritation - 0.8940 89.40%
Skin irritation - 0.7132 71.32%
Skin corrosion - 0.7829 78.29%
Ames mutagenesis - 0.5961 59.61%
Human Ether-a-go-go-Related Gene inhibition - 0.3739 37.39%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5935 59.35%
skin sensitisation - 0.8040 80.40%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.7304 73.04%
Acute Oral Toxicity (c) III 0.5598 55.98%
Estrogen receptor binding + 0.9001 90.01%
Androgen receptor binding + 0.7442 74.42%
Thyroid receptor binding + 0.6465 64.65%
Glucocorticoid receptor binding + 0.6746 67.46%
Aromatase binding + 0.7475 74.75%
PPAR gamma + 0.5846 58.46%
Honey bee toxicity - 0.8505 85.05%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.8360 83.60%

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 98.68% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 98.02% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.76% 97.25%
CHEMBL204 P00734 Thrombin 97.76% 96.01%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.94% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 96.10% 95.93%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.73% 96.38%
CHEMBL236 P41143 Delta opioid receptor 90.35% 99.35%
CHEMBL237 P41145 Kappa opioid receptor 89.78% 98.10%
CHEMBL268 P43235 Cathepsin K 89.53% 96.85%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.48% 96.61%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.41% 92.86%
CHEMBL2581 P07339 Cathepsin D 89.26% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 86.88% 98.03%
CHEMBL284 P27487 Dipeptidyl peptidase IV 86.86% 95.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.98% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.93% 91.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.21% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.78% 95.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.93% 100.00%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 83.15% 97.50%
CHEMBL2801 Q13557 CaM kinase II delta 83.09% 84.49%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.37% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.76% 96.77%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.21% 92.88%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 81.08% 95.27%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.90% 94.45%
CHEMBL206 P03372 Estrogen receptor alpha 80.70% 97.64%

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.
Buxus sempervirens

Cross-Links

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PubChem 162981415
LOTUS LTS0076595
wikiData Q105280130