Oleoyl danshenxinkun A

Details

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Internal ID d1b3c694-ab5c-4a74-bbba-cdb99960cc2a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Tanshinones, isotanshinones, and derivatives
IUPAC Name 2-(1-hydroxy-8-methyl-3,4-dioxophenanthren-2-yl)propyl (Z)-octadec-9-enoate
SMILES (Canonical) CCCCCCCCC=CCCCCCCCC(=O)OCC(C)C1=C(C2=C(C3=CC=CC(=C3C=C2)C)C(=O)C1=O)O
SMILES (Isomeric) CCCCCCCC/C=C\CCCCCCCC(=O)OCC(C)C1=C(C2=C(C3=CC=CC(=C3C=C2)C)C(=O)C1=O)O
InChI InChI=1S/C36H48O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-31(37)41-25-27(3)32-34(38)30-24-23-28-26(2)20-19-21-29(28)33(30)36(40)35(32)39/h11-12,19-21,23-24,27,38H,4-10,13-18,22,25H2,1-3H3/b12-11-
InChI Key GENQRBVLYJXZQU-QXMHVHEDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C36H48O5
Molecular Weight 560.80 g/mol
Exact Mass 560.35017463 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 10.40
Atomic LogP (AlogP) 9.40
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 18

Synonyms

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CHEBI:66819
2-(3-hydroxy-8-methyl-1,4-dioxo-1,4-dihydrophenanthren-2-yl)propyl (9Z)-octadec-9-enoate
16-O-oleoyl danshenxinkun A
CHEMBL473262
Q27135452
2-(1-hydroxy-8-methyl-3,4-dioxophenanthren-2-yl)propyl (Z)-octadec-9-enoate

2D Structure

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2D Structure of Oleoyl danshenxinkun A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.7104 71.04%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8352 83.52%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.7874 78.74%
OATP1B3 inhibitior + 0.9238 92.38%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9689 96.89%
P-glycoprotein inhibitior + 0.7907 79.07%
P-glycoprotein substrate + 0.5253 52.53%
CYP3A4 substrate + 0.6575 65.75%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.8930 89.30%
CYP3A4 inhibition - 0.6155 61.55%
CYP2C9 inhibition - 0.6739 67.39%
CYP2C19 inhibition + 0.5737 57.37%
CYP2D6 inhibition - 0.8280 82.80%
CYP1A2 inhibition + 0.7404 74.04%
CYP2C8 inhibition + 0.6465 64.65%
CYP inhibitory promiscuity - 0.6192 61.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6595 65.95%
Eye corrosion - 0.9946 99.46%
Eye irritation - 0.9154 91.54%
Skin irritation - 0.6971 69.71%
Skin corrosion - 0.9701 97.01%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6694 66.94%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5391 53.91%
skin sensitisation - 0.8691 86.91%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8454 84.54%
Acute Oral Toxicity (c) III 0.5626 56.26%
Estrogen receptor binding + 0.7321 73.21%
Androgen receptor binding + 0.7325 73.25%
Thyroid receptor binding - 0.6387 63.87%
Glucocorticoid receptor binding + 0.6756 67.56%
Aromatase binding - 0.5763 57.63%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9174 91.74%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6942 69.42%
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
CHEMBL2581 P07339 Cathepsin D 99.61% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.71% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.56% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.33% 95.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.46% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.71% 92.08%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.88% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.85% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 93.82% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 93.45% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.92% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.91% 93.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 89.47% 93.03%
CHEMBL1781 P11387 DNA topoisomerase I 89.28% 97.00%
CHEMBL2535 P11166 Glucose transporter 89.24% 98.75%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.61% 97.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.25% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.15% 96.09%
CHEMBL299 P17252 Protein kinase C alpha 84.85% 98.03%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.82% 96.47%
CHEMBL230 P35354 Cyclooxygenase-2 84.77% 89.63%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.52% 91.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.47% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 82.01% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 80.76% 97.79%

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 miltiorrhiza

Cross-Links

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PubChem 10415411
NPASS NPC30480
LOTUS LTS0209721
wikiData Q105007242