(1R,3R,3aR,4R,5aS,7aR,9R,11aS,13aS,13bS)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysene-1,4,9-triol

Details

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Internal ID 05ab6b97-8245-4853-aade-a35f8fd9682c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,3R,3aR,4R,5aS,7aR,9R,11aS,13aS,13bS)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysene-1,4,9-triol
SMILES (Canonical) CC(C)C1CC(C2C1(C(CC3(C2(CC=C4C3=CCC5C4(CCC(C5(C)C)O)C)C)C)O)C)O
SMILES (Isomeric) CC(C)[C@H]1C[C@H]([C@@H]2[C@@]1([C@@H](C[C@]3([C@]2(CC=C4C3=CC[C@@H]5[C@@]4(CC[C@H](C5(C)C)O)C)C)C)O)C)O
InChI InChI=1S/C30H48O3/c1-17(2)20-15-21(31)25-28(6)14-11-18-19(29(28,7)16-24(33)30(20,25)8)9-10-22-26(3,4)23(32)12-13-27(18,22)5/h9,11,17,20-25,31-33H,10,12-16H2,1-8H3/t20-,21-,22+,23-,24-,25+,27-,28+,29-,30+/m1/s1
InChI Key JKYBCDCVXDIGHM-BZDGEACKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O3
Molecular Weight 456.70 g/mol
Exact Mass 456.36034539 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.89
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,3R,3aR,4R,5aS,7aR,9R,11aS,13aS,13bS)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysene-1,4,9-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5065 50.65%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6838 68.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.6393 63.93%
P-glycoprotein inhibitior - 0.6546 65.46%
P-glycoprotein substrate - 0.5711 57.11%
CYP3A4 substrate + 0.6457 64.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7337 73.37%
CYP3A4 inhibition - 0.8741 87.41%
CYP2C9 inhibition - 0.9130 91.30%
CYP2C19 inhibition - 0.8936 89.36%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.9024 90.24%
CYP2C8 inhibition - 0.6028 60.28%
CYP inhibitory promiscuity - 0.7172 71.72%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5463 54.63%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.9410 94.10%
Skin irritation + 0.6084 60.84%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4696 46.96%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation + 0.4728 47.28%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity - 0.7525 75.25%
Acute Oral Toxicity (c) III 0.6265 62.65%
Estrogen receptor binding + 0.7032 70.32%
Androgen receptor binding + 0.6881 68.81%
Thyroid receptor binding + 0.6659 66.59%
Glucocorticoid receptor binding + 0.7501 75.01%
Aromatase binding + 0.6665 66.65%
PPAR gamma + 0.5774 57.74%
Honey bee toxicity - 0.7570 75.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9905 99.05%

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 97.55% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.27% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 93.11% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.41% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.24% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.21% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.12% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.81% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.55% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.36% 95.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.94% 85.31%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.72% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.53% 93.56%
CHEMBL1871 P10275 Androgen Receptor 82.46% 96.43%
CHEMBL221 P23219 Cyclooxygenase-1 82.29% 90.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.09% 97.14%
CHEMBL4444 P04070 Vitamin K-dependent protein C 81.49% 93.89%
CHEMBL2996 Q05655 Protein kinase C delta 81.14% 97.79%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.87% 96.61%

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.
Lonicera gracilipes

Cross-Links

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PubChem 10695139
LOTUS LTS0169041
wikiData Q105130570