4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,8,13-triol

Details

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Internal ID ec30c6a1-445d-40f8-b7af-7b185e733c9e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,8,13-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H50O3/c1-17-9-12-28(6)23(33)16-30(8)25(24(28)18(17)2)19(31)15-21-27(5)13-11-22(32)26(3,4)20(27)10-14-29(21,30)7/h9,18-25,31-33H,10-16H2,1-8H3
InChI Key CRZWSLHKMJNXGP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O3
Molecular Weight 458.70 g/mol
Exact Mass 458.37599545 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.97
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,8,13-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 - 0.5970 59.70%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6811 68.11%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.8943 89.43%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.7440 74.40%
P-glycoprotein inhibitior - 0.6793 67.93%
P-glycoprotein substrate - 0.7059 70.59%
CYP3A4 substrate + 0.6862 68.62%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.7120 71.20%
CYP2C9 inhibition - 0.9058 90.58%
CYP2C19 inhibition - 0.8555 85.55%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition - 0.8976 89.76%
CYP2C8 inhibition - 0.5961 59.61%
CYP inhibitory promiscuity - 0.7803 78.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5954 59.54%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9310 93.10%
Skin irritation + 0.5517 55.17%
Skin corrosion - 0.9646 96.46%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4275 42.75%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.6288 62.88%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8737 87.37%
Acute Oral Toxicity (c) III 0.7557 75.57%
Estrogen receptor binding + 0.8206 82.06%
Androgen receptor binding + 0.7546 75.46%
Thyroid receptor binding + 0.6609 66.09%
Glucocorticoid receptor binding + 0.7436 74.36%
Aromatase binding + 0.7398 73.98%
PPAR gamma + 0.5735 57.35%
Honey bee toxicity - 0.7787 77.87%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9886 98.86%

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 92.52% 96.09%
CHEMBL1871 P10275 Androgen Receptor 92.09% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.28% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.69% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.23% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.45% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.90% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 85.48% 90.17%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.49% 86.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.18% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 83.06% 97.79%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.91% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.14% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.27% 91.11%

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.
Cicuta virosa

Cross-Links

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PubChem 162940505
LOTUS LTS0092638
wikiData Q104969040