CID 85190129

Details

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Internal ID d09d323d-607a-4b8e-85a2-85b21fbc40f5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC1CC(C2C(CCCC2(C13CCC4(O3)CC(OC4)OC)C)(C)C)OC(=O)C
SMILES (Isomeric) CC1CC(C2C(CCCC2(C13CCC4(O3)CC(OC4)OC)C)(C)C)OC(=O)C
InChI InChI=1S/C23H38O5/c1-15-12-17(27-16(2)24)19-20(3,4)8-7-9-21(19,5)23(15)11-10-22(28-23)13-18(25-6)26-14-22/h15,17-19H,7-14H2,1-6H3
InChI Key FZZTZQBZRHIDKL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H38O5
Molecular Weight 394.50 g/mol
Exact Mass 394.27192431 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.47
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 85190129

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9851 98.51%
Caco-2 + 0.6202 62.02%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7412 74.12%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8626 86.26%
OATP1B3 inhibitior + 0.9656 96.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.6137 61.37%
P-glycoprotein inhibitior - 0.5625 56.25%
P-glycoprotein substrate - 0.6262 62.62%
CYP3A4 substrate + 0.6981 69.81%
CYP2C9 substrate - 0.8185 81.85%
CYP2D6 substrate - 0.8782 87.82%
CYP3A4 inhibition - 0.8662 86.62%
CYP2C9 inhibition - 0.7336 73.36%
CYP2C19 inhibition - 0.7003 70.03%
CYP2D6 inhibition - 0.9093 90.93%
CYP1A2 inhibition - 0.8975 89.75%
CYP2C8 inhibition + 0.5396 53.96%
CYP inhibitory promiscuity - 0.9296 92.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5684 56.84%
Eye corrosion - 0.9800 98.00%
Eye irritation - 0.8260 82.60%
Skin irritation - 0.8380 83.80%
Skin corrosion - 0.9562 95.62%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5097 50.97%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.6449 64.49%
skin sensitisation - 0.8634 86.34%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6313 63.13%
Acute Oral Toxicity (c) III 0.6056 60.56%
Estrogen receptor binding + 0.8773 87.73%
Androgen receptor binding + 0.6685 66.85%
Thyroid receptor binding + 0.7508 75.08%
Glucocorticoid receptor binding + 0.7336 73.36%
Aromatase binding + 0.7810 78.10%
PPAR gamma + 0.6908 69.08%
Honey bee toxicity - 0.6807 68.07%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9246 92.46%

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 97.52% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.41% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.43% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.97% 85.14%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 89.71% 95.71%
CHEMBL340 P08684 Cytochrome P450 3A4 89.23% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.84% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.34% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.91% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.44% 99.23%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.98% 89.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.41% 86.33%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.26% 97.28%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.28% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.93% 91.07%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.71% 95.71%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.93% 95.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.25% 82.69%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.52% 97.14%

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.
Vitex agnus-castus

Cross-Links

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PubChem 85190129
LOTUS LTS0014162
wikiData Q105005277