(3aR,5bR,11aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-13-one

Details

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Internal ID 8830712a-0f9d-4105-866e-64a3b15150e4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3aR,5bR,11aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-13-one
SMILES (Canonical) CC(C)C1CCC2(C1C3C(=O)CC4C5(CCCC(C5CCC4(C3(CC2)C)C)(C)C)C)C
SMILES (Isomeric) CC(C)C1CC[C@]2(C1C3C(=O)CC4[C@]5(CCCC(C5CC[C@]4(C3(CC2)C)C)(C)C)C)C
InChI InChI=1S/C30H50O/c1-19(2)20-10-14-27(5)16-17-30(8)25(24(20)27)21(31)18-23-28(6)13-9-12-26(3,4)22(28)11-15-29(23,30)7/h19-20,22-25H,9-18H2,1-8H3/t20?,22?,23?,24?,25?,27-,28+,29-,30?/m1/s1
InChI Key QDEOBJOJWNHBGH-MRPFRCTHSA-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) 17.10 Ų
XlogP 9.80
Atomic LogP (AlogP) 8.31
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3aR,5bR,11aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,9,10,11,11b,12,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-13-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.6350 63.50%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5716 57.16%
OATP2B1 inhibitior - 0.8636 86.36%
OATP1B1 inhibitior + 0.8954 89.54%
OATP1B3 inhibitior + 0.9788 97.88%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6181 61.81%
P-glycoprotein inhibitior - 0.5864 58.64%
P-glycoprotein substrate - 0.8107 81.07%
CYP3A4 substrate + 0.6197 61.97%
CYP2C9 substrate - 0.7813 78.13%
CYP2D6 substrate - 0.7531 75.31%
CYP3A4 inhibition - 0.9232 92.32%
CYP2C9 inhibition - 0.8429 84.29%
CYP2C19 inhibition - 0.8244 82.44%
CYP2D6 inhibition - 0.9736 97.36%
CYP1A2 inhibition - 0.8671 86.71%
CYP2C8 inhibition - 0.7104 71.04%
CYP inhibitory promiscuity - 0.9369 93.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5830 58.30%
Eye corrosion - 0.9494 94.94%
Eye irritation - 0.8445 84.45%
Skin irritation + 0.7030 70.30%
Skin corrosion - 0.9215 92.15%
Ames mutagenesis - 0.7123 71.23%
Human Ether-a-go-go-Related Gene inhibition - 0.5754 57.54%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.8563 85.63%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6149 61.49%
Acute Oral Toxicity (c) III 0.7234 72.34%
Estrogen receptor binding + 0.8320 83.20%
Androgen receptor binding + 0.7710 77.10%
Thyroid receptor binding + 0.5714 57.14%
Glucocorticoid receptor binding + 0.7951 79.51%
Aromatase binding + 0.6684 66.84%
PPAR gamma + 0.6038 60.38%
Honey bee toxicity - 0.7669 76.69%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9703 97.03%

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
CHEMBL1937 Q92769 Histone deacetylase 2 95.57% 94.75%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 94.44% 96.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.29% 94.45%
CHEMBL3524 P56524 Histone deacetylase 4 92.94% 92.97%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.91% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.91% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.27% 95.89%
CHEMBL4302 P08183 P-glycoprotein 1 89.73% 92.98%
CHEMBL2581 P07339 Cathepsin D 89.58% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.10% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.04% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.66% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.95% 91.11%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.59% 95.71%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.41% 99.18%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.99% 93.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.80% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.10% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.79% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.42% 93.99%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 83.01% 100.00%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.61% 91.38%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.63% 91.24%
CHEMBL1871 P10275 Androgen Receptor 80.11% 96.43%

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.
Clerodendrum trichotomum

Cross-Links

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PubChem 5315973
NPASS NPC281519