[(3S,3aS,5aR,5bR,7aS,9S,11R,11aR,11bS,13aR,13bS)-11-hydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate

Details

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Internal ID a9efcbc6-6742-44fd-a14e-4c62ee4027e3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Hopanoids
IUPAC Name [(3S,3aS,5aR,5bR,7aS,9S,11R,11aR,11bS,13aR,13bS)-11-hydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H54O4/c1-19(33)36-26-18-25(34)32(9)22(27(26,2)3)14-17-31(8)24(32)11-10-23-29(6)15-12-20(28(4,5)35)21(29)13-16-30(23,31)7/h20-26,34-35H,10-18H2,1-9H3/t20-,21-,22-,23+,24-,25+,26-,29-,30+,31+,32-/m0/s1
InChI Key IMYHRRRRCHBQMZ-HHTMWPDDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H54O4
Molecular Weight 502.80 g/mol
Exact Mass 502.40221020 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 8.00
Atomic LogP (AlogP) 6.76
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(3S,3aS,5aR,5bR,7aS,9S,11R,11aR,11bS,13aR,13bS)-11-hydroxy-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-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 + 0.9902 99.02%
Caco-2 - 0.7219 72.19%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8058 80.58%
OATP2B1 inhibitior - 0.5695 56.95%
OATP1B1 inhibitior + 0.8485 84.85%
OATP1B3 inhibitior + 0.8292 82.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8571 85.71%
BSEP inhibitior + 0.6359 63.59%
P-glycoprotein inhibitior - 0.4853 48.53%
P-glycoprotein substrate - 0.8084 80.84%
CYP3A4 substrate + 0.7320 73.20%
CYP2C9 substrate - 0.8254 82.54%
CYP2D6 substrate - 0.8496 84.96%
CYP3A4 inhibition - 0.8695 86.95%
CYP2C9 inhibition - 0.7723 77.23%
CYP2C19 inhibition - 0.8419 84.19%
CYP2D6 inhibition - 0.9770 97.70%
CYP1A2 inhibition - 0.6568 65.68%
CYP2C8 inhibition + 0.5145 51.45%
CYP inhibitory promiscuity - 0.9643 96.43%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9232 92.32%
Skin irritation + 0.6705 67.05%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis - 0.7654 76.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5181 51.81%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.7056 70.56%
skin sensitisation - 0.7990 79.90%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7335 73.35%
Acute Oral Toxicity (c) I 0.5155 51.55%
Estrogen receptor binding + 0.6914 69.14%
Androgen receptor binding + 0.7224 72.24%
Thyroid receptor binding + 0.5766 57.66%
Glucocorticoid receptor binding + 0.6666 66.66%
Aromatase binding + 0.7382 73.82%
PPAR gamma + 0.6454 64.54%
Honey bee toxicity - 0.5662 56.62%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9884 98.84%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.12% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.34% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.03% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.48% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.64% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.47% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.41% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.73% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.27% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.03% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.78% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.40% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 83.76% 91.19%
CHEMBL5028 O14672 ADAM10 82.36% 97.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.11% 97.14%
CHEMBL2996 Q05655 Protein kinase C delta 81.55% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.06% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.63% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.32% 92.94%

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.
There are no matching plants.

Cross-Links

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PubChem 163078612
LOTUS LTS0012338
wikiData Q105115997