2,2,4a,6a,6a,9,9,14a-Octamethyl-1,3,4,5,6,6b,7,10,11,12,12a,13,14,14b-tetradecahydropicen-1-ol

Details

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Internal ID 6b32bddb-5660-4b02-9cee-a2a87a2d2f4d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 2,2,4a,6a,6a,9,9,14a-octamethyl-1,3,4,5,6,6b,7,10,11,12,12a,13,14,14b-tetradecahydropicen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H50O/c1-25(2)13-9-10-21-20(25)11-12-22-28(21,6)17-19-30(8)23-24(31)26(3,4)14-15-27(23,5)16-18-29(22,30)7/h11,21-24,31H,9-10,12-19H2,1-8H3
InChI Key CBKBMXNYFWWHKR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O
Molecular Weight 426.70 g/mol
Exact Mass 426.386166214 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 9.30
Atomic LogP (AlogP) 8.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,2,4a,6a,6a,9,9,14a-Octamethyl-1,3,4,5,6,6b,7,10,11,12,12a,13,14,14b-tetradecahydropicen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.5745 57.45%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5452 54.52%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.8838 88.38%
OATP1B3 inhibitior + 0.9145 91.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8941 89.41%
P-glycoprotein inhibitior - 0.7561 75.61%
P-glycoprotein substrate - 0.8465 84.65%
CYP3A4 substrate + 0.5769 57.69%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.8304 83.04%
CYP2C9 inhibition - 0.6113 61.13%
CYP2C19 inhibition - 0.5375 53.75%
CYP2D6 inhibition - 0.9288 92.88%
CYP1A2 inhibition - 0.7440 74.40%
CYP2C8 inhibition - 0.6271 62.71%
CYP inhibitory promiscuity - 0.6420 64.20%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5800 58.00%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.9330 93.30%
Skin irritation + 0.5815 58.15%
Skin corrosion - 0.9428 94.28%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8037 80.37%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5959 59.59%
skin sensitisation + 0.6992 69.92%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.4514 45.14%
Acute Oral Toxicity (c) III 0.6673 66.73%
Estrogen receptor binding + 0.8402 84.02%
Androgen receptor binding + 0.6971 69.71%
Thyroid receptor binding + 0.6888 68.88%
Glucocorticoid receptor binding + 0.8229 82.29%
Aromatase binding + 0.7153 71.53%
PPAR gamma + 0.5938 59.38%
Honey bee toxicity - 0.8723 87.23%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9964 99.64%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.55% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.65% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.15% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.07% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.94% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.68% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.30% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.01% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.61% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.40% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.96% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 80.73% 98.95%
CHEMBL4208 P20618 Proteasome component C5 80.52% 90.00%

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.
Euonymus hamiltonianus

Cross-Links

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PubChem 162939410
LOTUS LTS0003673
wikiData Q104952453