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

Details

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Internal ID 4a3b7d85-c7bf-4474-8cd9-1273c1599724
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(2R,3R,4aR,6aS,6bR,8aS,11S,12R,12aR,14bS)-2,11-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-yl] acetate
SMILES (Canonical) CC1C2C3=CC=C4C(C3(CCC2(CCC1(C)O)C)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C
SMILES (Isomeric) C[C@@H]1[C@H]2C3=CC=C4[C@]([C@@]3(CC[C@]2(CC[C@]1(C)O)C)C)(CC[C@@H]5[C@@]4(C[C@H]([C@@H](C5(C)C)OC(=O)C)O)C)C
InChI InChI=1S/C32H50O4/c1-19-25-21-10-11-24-29(6)18-22(34)26(36-20(2)33)27(3,4)23(29)12-13-31(24,8)30(21,7)16-14-28(25,5)15-17-32(19,9)35/h10-11,19,22-23,25-26,34-35H,12-18H2,1-9H3/t19-,22-,23+,25+,26+,28+,29+,30-,31-,32+/m1/s1
InChI Key KWEUMHZBJOUIDF-PMIIATRGSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C32H50O4
Molecular Weight 498.70 g/mol
Exact Mass 498.37091007 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.60
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3R,4aR,6aS,6bR,8aS,11S,12R,12aR,14bS)-2,11-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicen-3-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 + 0.9957 99.57%
Caco-2 - 0.5758 57.58%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8614 86.14%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8913 89.13%
OATP1B3 inhibitior + 0.8634 86.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6543 65.43%
P-glycoprotein inhibitior + 0.5960 59.60%
P-glycoprotein substrate - 0.5666 56.66%
CYP3A4 substrate + 0.6922 69.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8815 88.15%
CYP3A4 inhibition - 0.8345 83.45%
CYP2C9 inhibition - 0.8585 85.85%
CYP2C19 inhibition - 0.9226 92.26%
CYP2D6 inhibition - 0.9449 94.49%
CYP1A2 inhibition - 0.9004 90.04%
CYP2C8 inhibition - 0.5856 58.56%
CYP inhibitory promiscuity - 0.9467 94.67%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9743 97.43%
Carcinogenicity (trinary) Non-required 0.6567 65.67%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.9418 94.18%
Skin irritation + 0.5438 54.38%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis - 0.7870 78.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6426 64.26%
skin sensitisation - 0.5911 59.11%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4965 49.65%
Estrogen receptor binding + 0.7074 70.74%
Androgen receptor binding + 0.7343 73.43%
Thyroid receptor binding + 0.6548 65.48%
Glucocorticoid receptor binding + 0.7263 72.63%
Aromatase binding + 0.7189 71.89%
PPAR gamma + 0.5752 57.52%
Honey bee toxicity - 0.6361 63.61%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5255 52.55%
Fish aquatic toxicity + 0.9951 99.51%

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 96.19% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.14% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.09% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.63% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 90.86% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.51% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.09% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.50% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.90% 100.00%
CHEMBL2581 P07339 Cathepsin D 87.65% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.12% 97.21%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.85% 91.07%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.10% 92.94%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.00% 91.24%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.98% 93.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.68% 90.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.52% 85.30%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.14% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.02% 95.50%

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.
Salvia kronenburgii

Cross-Links

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PubChem 21600001
LOTUS LTS0263119
wikiData Q105146894