10-Hydroxy-2,4a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,6a-dicarboxylic acid

Details

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Internal ID bacd7209-5ab5-4114-abaa-492d5aab7124
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 10-hydroxy-2,4a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,6a-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H46O5/c1-25(2)20-9-12-29(6)21(28(20,5)11-10-22(25)31)8-7-18-19-17-27(4,23(32)33)14-13-26(19,3)15-16-30(18,29)24(34)35/h7,19-22,31H,8-17H2,1-6H3,(H,32,33)(H,34,35)
InChI Key QEZXREBSGZAJJO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O5
Molecular Weight 486.70 g/mol
Exact Mass 486.33452456 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 6.00
Atomic LogP (AlogP) 6.30
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Hydroxy-2,4a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,6a-dicarboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 - 0.6339 63.39%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8912 89.12%
OATP2B1 inhibitior - 0.7143 71.43%
OATP1B1 inhibitior + 0.8245 82.45%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5321 53.21%
BSEP inhibitior + 0.8729 87.29%
P-glycoprotein inhibitior - 0.6689 66.89%
P-glycoprotein substrate - 0.8583 85.83%
CYP3A4 substrate + 0.6564 65.64%
CYP2C9 substrate - 0.8404 84.04%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.9317 93.17%
CYP2C19 inhibition - 0.9604 96.04%
CYP2D6 inhibition - 0.9538 95.38%
CYP1A2 inhibition - 0.9296 92.96%
CYP2C8 inhibition - 0.6815 68.15%
CYP inhibitory promiscuity - 0.9544 95.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6941 69.41%
Eye corrosion - 0.9945 99.45%
Eye irritation - 0.9371 93.71%
Skin irritation + 0.6462 64.62%
Skin corrosion - 0.9582 95.82%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3633 36.33%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation + 0.5247 52.47%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.5428 54.28%
Acute Oral Toxicity (c) III 0.8402 84.02%
Estrogen receptor binding + 0.7355 73.55%
Androgen receptor binding + 0.6762 67.62%
Thyroid receptor binding + 0.5513 55.13%
Glucocorticoid receptor binding + 0.8638 86.38%
Aromatase binding + 0.7116 71.16%
PPAR gamma + 0.5815 58.15%
Honey bee toxicity - 0.8664 86.64%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9975 99.75%

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
CHEMBL221 P23219 Cyclooxygenase-1 97.03% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.41% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.10% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.85% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.15% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.66% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.96% 93.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.61% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.23% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.62% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.63% 82.69%

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.
Cordia alliodora

Cross-Links

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PubChem 73810238
LOTUS LTS0038589
wikiData Q105219452