(ent-15beta)-15-Hydroxy-19-trachylobanoic acid

Details

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Internal ID 9cd7e339-dd19-44dc-8742-0fb425494778
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name 16-hydroxy-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid
SMILES (Canonical) CC12CCCC(C1CCC34C2CC5C(C3)C5(C4O)C)(C)C(=O)O
SMILES (Isomeric) CC12CCCC(C1CCC34C2CC5C(C3)C5(C4O)C)(C)C(=O)O
InChI InChI=1S/C20H30O3/c1-17-6-4-7-18(2,16(22)23)13(17)5-8-20-10-12-11(9-14(17)20)19(12,3)15(20)21/h11-15,21H,4-10H2,1-3H3,(H,22,23)
InChI Key MHVNHDYWKUKRRJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O3
Molecular Weight 318.40 g/mol
Exact Mass 318.21949481 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (ent-15beta)-15-Hydroxy-19-trachylobanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.6402 64.02%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7530 75.30%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8626 86.26%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.5166 51.66%
P-glycoprotein inhibitior - 0.7662 76.62%
P-glycoprotein substrate - 0.8227 82.27%
CYP3A4 substrate + 0.6249 62.49%
CYP2C9 substrate - 0.6762 67.62%
CYP2D6 substrate - 0.8321 83.21%
CYP3A4 inhibition - 0.8251 82.51%
CYP2C9 inhibition - 0.6878 68.78%
CYP2C19 inhibition - 0.8608 86.08%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.5757 57.57%
CYP2C8 inhibition - 0.7490 74.90%
CYP inhibitory promiscuity - 0.9274 92.74%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6175 61.75%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.8980 89.80%
Skin irritation + 0.5674 56.74%
Skin corrosion - 0.9400 94.00%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7420 74.20%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.7015 70.15%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6114 61.14%
Acute Oral Toxicity (c) III 0.5177 51.77%
Estrogen receptor binding + 0.8667 86.67%
Androgen receptor binding + 0.5306 53.06%
Thyroid receptor binding + 0.6905 69.05%
Glucocorticoid receptor binding + 0.7985 79.85%
Aromatase binding + 0.7299 72.99%
PPAR gamma - 0.5465 54.65%
Honey bee toxicity - 0.8541 85.41%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9945 99.45%

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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 97.14% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.06% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.87% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 90.79% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 87.17% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.13% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.68% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.40% 93.04%
CHEMBL237 P41145 Kappa opioid receptor 82.17% 98.10%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.46% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.32% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.14% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.34% 93.03%

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.
Helianthus annuus
Xylopia aethiopica

Cross-Links

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PubChem 131752061
LOTUS LTS0129274
wikiData Q105164250