[(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-3-oxo-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-yl] acetate

Details

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Internal ID 2f1c33d6-f7de-4b6d-bcd9-f058570bd381
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-3-oxo-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-yl] acetate
SMILES (Canonical) CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C
SMILES (Isomeric) C[C@H]1C(=O)[C@H](C[C@@H]2[C@@]1(CC[C@H]3[C@]2(CC[C@@]4([C@@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C
InChI InChI=1S/C32H52O3/c1-20-26(34)22(35-21(2)33)18-24-29(20,6)11-10-23-30(24,7)15-17-32(9)25-19-27(3,4)12-13-28(25,5)14-16-31(23,32)8/h20,22-25H,10-19H2,1-9H3/t20-,22-,23-,24+,25+,28+,29+,30+,31+,32-/m0/s1
InChI Key BSEZSGNYRAQMJE-UPOUNKDHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H52O3
Molecular Weight 484.80 g/mol
Exact Mass 484.39164552 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 9.80
Atomic LogP (AlogP) 8.00
H-Bond Acceptor 3
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 [(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-3-oxo-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 - 0.6334 63.34%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8491 84.91%
OATP2B1 inhibitior - 0.7178 71.78%
OATP1B1 inhibitior + 0.8868 88.68%
OATP1B3 inhibitior + 0.9872 98.72%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8827 88.27%
P-glycoprotein inhibitior + 0.6161 61.61%
P-glycoprotein substrate - 0.7407 74.07%
CYP3A4 substrate + 0.6832 68.32%
CYP2C9 substrate - 0.7941 79.41%
CYP2D6 substrate - 0.8488 84.88%
CYP3A4 inhibition - 0.8606 86.06%
CYP2C9 inhibition - 0.8211 82.11%
CYP2C19 inhibition - 0.7301 73.01%
CYP2D6 inhibition - 0.9660 96.60%
CYP1A2 inhibition - 0.9075 90.75%
CYP2C8 inhibition - 0.7239 72.39%
CYP inhibitory promiscuity - 0.9687 96.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5659 56.59%
Eye corrosion - 0.9755 97.55%
Eye irritation - 0.8859 88.59%
Skin irritation - 0.5892 58.92%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7454 74.54%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.7197 71.97%
skin sensitisation - 0.5825 58.25%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6784 67.84%
Acute Oral Toxicity (c) III 0.7109 71.09%
Estrogen receptor binding + 0.7126 71.26%
Androgen receptor binding + 0.6460 64.60%
Thyroid receptor binding + 0.6345 63.45%
Glucocorticoid receptor binding + 0.7561 75.61%
Aromatase binding + 0.7262 72.62%
PPAR gamma + 0.6312 63.12%
Honey bee toxicity - 0.7431 74.31%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9920 99.20%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.42% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.59% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.58% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.35% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.22% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.03% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.32% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.78% 96.38%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.42% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.20% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.85% 93.03%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.73% 91.03%
CHEMBL340 P08684 Cytochrome P450 3A4 81.69% 91.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.05% 91.07%
CHEMBL237 P41145 Kappa opioid receptor 80.74% 98.10%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.49% 94.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.38% 89.00%

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.
Allium neapolitanum
Cycas armstrongii
Cycas revoluta
Ephedra aphylla
Licaria armeniaca
Mammillaria magnimamma
Munronia pinnata
Plectocephalus chilensis
Quercus suber
Trichilia hirta
Typha domingensis

Cross-Links

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PubChem 14465799
NPASS NPC263964