2,3-o-Diacetylcorosolic acid

Details

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Internal ID 7f3b8851-7fe9-48f7-b6e7-ce449e14b1e9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 10,11-diacetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H52O6/c1-19-12-15-34(29(37)38)17-16-32(8)23(27(34)20(19)2)10-11-26-31(7)18-24(39-21(3)35)28(40-22(4)36)30(5,6)25(31)13-14-33(26,32)9/h10,19-20,24-28H,11-18H2,1-9H3,(H,37,38)
InChI Key LHSSNRACHZBMIY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H52O6
Molecular Weight 556.80 g/mol
Exact Mass 556.37638937 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 7.50
Atomic LogP (AlogP) 7.20
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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57498-76-7

2D Structure

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2D Structure of 2,3-o-Diacetylcorosolic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 - 0.7357 73.57%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.9041 90.41%
OATP2B1 inhibitior - 0.7168 71.68%
OATP1B1 inhibitior + 0.8146 81.46%
OATP1B3 inhibitior - 0.5000 50.00%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5821 58.21%
BSEP inhibitior + 0.8449 84.49%
P-glycoprotein inhibitior + 0.7684 76.84%
P-glycoprotein substrate - 0.6899 68.99%
CYP3A4 substrate + 0.6839 68.39%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8818 88.18%
CYP3A4 inhibition - 0.8055 80.55%
CYP2C9 inhibition - 0.8521 85.21%
CYP2C19 inhibition - 0.8589 85.89%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition - 0.7291 72.91%
CYP2C8 inhibition + 0.6254 62.54%
CYP inhibitory promiscuity - 0.9394 93.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9843 98.43%
Carcinogenicity (trinary) Non-required 0.6579 65.79%
Eye corrosion - 0.9933 99.33%
Eye irritation - 0.9225 92.25%
Skin irritation + 0.5920 59.20%
Skin corrosion - 0.9626 96.26%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4625 46.25%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.6202 62.02%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6488 64.88%
Acute Oral Toxicity (c) III 0.5919 59.19%
Estrogen receptor binding + 0.6668 66.68%
Androgen receptor binding + 0.7400 74.00%
Thyroid receptor binding + 0.5836 58.36%
Glucocorticoid receptor binding + 0.7987 79.87%
Aromatase binding + 0.7448 74.48%
PPAR gamma + 0.6379 63.79%
Honey bee toxicity - 0.7322 73.22%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5505 55.05%
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 94.90% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.43% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.91% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.15% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 88.75% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.58% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.29% 93.00%
CHEMBL2581 P07339 Cathepsin D 84.78% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.26% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 83.62% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.67% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.96% 100.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.80% 94.08%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.42% 85.30%

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.
Prunus zippeliana

Cross-Links

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PubChem 73022349
LOTUS LTS0240928
wikiData Q105151935