CID 162996555

Details

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Internal ID cecb6547-6e38-4ee9-8cfd-76699dfcc428
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H78N2O7/c1-27-45-41(61-53(27)17-15-48(5,59)26-60-53)20-35-31-12-10-29-18-37-39(24-49(29,6)33(31)22-43(57)51(35,45)8)55-38-19-30-11-13-32-34(50(30,7)25-40(38)56-37)23-44(58)52(9)36(32)21-42-46(52)28(2)54(62-42)16-14-47(3,4)63-54/h20,27-34,36,41-46,57-59H,10-19,21-26H2,1-9H3/t27-,28-,29-,30-,31+,32+,33-,34-,36+,41+,42-,43+,44-,45-,46-,48-,49-,50-,51+,52+,53+,54+/m0/s1
InChI Key OQFYYRHPDXZIHN-AYVSTLDZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C54H78N2O7
Molecular Weight 867.20 g/mol
Exact Mass 866.58090283 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 8.32
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162996555

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 - 0.8578 85.78%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5834 58.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8592 85.92%
OATP1B3 inhibitior + 0.9358 93.58%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9695 96.95%
P-glycoprotein inhibitior + 0.7583 75.83%
P-glycoprotein substrate + 0.7299 72.99%
CYP3A4 substrate + 0.7453 74.53%
CYP2C9 substrate - 0.8089 80.89%
CYP2D6 substrate - 0.7776 77.76%
CYP3A4 inhibition - 0.7658 76.58%
CYP2C9 inhibition - 0.8535 85.35%
CYP2C19 inhibition - 0.8436 84.36%
CYP2D6 inhibition - 0.8626 86.26%
CYP1A2 inhibition + 0.5132 51.32%
CYP2C8 inhibition + 0.7795 77.95%
CYP inhibitory promiscuity - 0.6742 67.42%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5363 53.63%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9059 90.59%
Skin irritation - 0.6980 69.80%
Skin corrosion - 0.9304 93.04%
Ames mutagenesis - 0.6437 64.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7370 73.70%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8229 82.29%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6496 64.96%
Acute Oral Toxicity (c) III 0.6378 63.78%
Estrogen receptor binding + 0.8117 81.17%
Androgen receptor binding + 0.7631 76.31%
Thyroid receptor binding + 0.5423 54.23%
Glucocorticoid receptor binding + 0.7512 75.12%
Aromatase binding + 0.6662 66.62%
PPAR gamma + 0.8025 80.25%
Honey bee toxicity - 0.6581 65.81%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9566 95.66%

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 97.21% 96.09%
CHEMBL2243 O00519 Anandamide amidohydrolase 91.29% 97.53%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.21% 100.00%
CHEMBL1914 P06276 Butyrylcholinesterase 91.10% 95.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.71% 97.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 90.47% 89.05%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.07% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.98% 85.14%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.11% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.02% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.95% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.38% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.86% 82.69%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 85.58% 96.39%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.33% 94.45%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.19% 98.99%
CHEMBL5028 O14672 ADAM10 81.77% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.13% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162996555
LOTUS LTS0010366
wikiData Q105196771