10-acetyloxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid

Details

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Internal ID 20f03f58-cb4d-4985-b340-bd0e95c49ea5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 10-acetyloxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H50O4/c1-19-11-14-29(6)17-18-32(27(34)35)22(26(29)20(19)2)9-10-24-30(7)15-13-25(36-21(3)33)28(4,5)23(30)12-16-31(24,32)8/h9,19-20,23-26H,10-18H2,1-8H3,(H,34,35)
InChI Key ZRCFPJAOYIOKMF-UHFFFAOYSA-N
Popularity 0 references 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) 63.60 Ų
XlogP 8.10
Atomic LogP (AlogP) 7.66
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-acetyloxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 - 0.5176 51.76%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.9143 91.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7331 73.31%
OATP1B3 inhibitior - 0.5699 56.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6071 60.71%
BSEP inhibitior + 0.8454 84.54%
P-glycoprotein inhibitior + 0.6294 62.94%
P-glycoprotein substrate - 0.7890 78.90%
CYP3A4 substrate + 0.6880 68.80%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8818 88.18%
CYP3A4 inhibition - 0.8067 80.67%
CYP2C9 inhibition - 0.8398 83.98%
CYP2C19 inhibition - 0.8914 89.14%
CYP2D6 inhibition - 0.9524 95.24%
CYP1A2 inhibition - 0.7163 71.63%
CYP2C8 inhibition + 0.5653 56.53%
CYP inhibitory promiscuity - 0.9277 92.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9843 98.43%
Carcinogenicity (trinary) Non-required 0.6575 65.75%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.9428 94.28%
Skin irritation + 0.5901 59.01%
Skin corrosion - 0.9664 96.64%
Ames mutagenesis - 0.7223 72.23%
Human Ether-a-go-go-Related Gene inhibition - 0.4200 42.00%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.7084 70.84%
skin sensitisation - 0.5494 54.94%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4709 47.09%
Acute Oral Toxicity (c) III 0.8121 81.21%
Estrogen receptor binding + 0.7299 72.99%
Androgen receptor binding + 0.7316 73.16%
Thyroid receptor binding + 0.5974 59.74%
Glucocorticoid receptor binding + 0.8059 80.59%
Aromatase binding + 0.7408 74.08%
PPAR gamma + 0.5899 58.99%
Honey bee toxicity - 0.8104 81.04%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5095 50.95%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.16% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.65% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.48% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 91.98% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.83% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.51% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 84.42% 91.19%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.70% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.53% 86.33%
CHEMBL5028 O14672 ADAM10 81.90% 97.50%
CHEMBL2581 P07339 Cathepsin D 81.88% 98.95%

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.
Astilbe rubra

Cross-Links

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PubChem 56668012
LOTUS LTS0099525
wikiData Q105381882