CID 162821194

Details

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Internal ID 1dd04e09-3011-4128-988f-c22faf6e8161
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical) CC1CC(C2C(CCCC2(C13CCC4(O3)CCOC4=O)C)(C)C)OC(=O)C
SMILES (Isomeric) C[C@@H]1C[C@@H]([C@@H]2[C@]([C@@]13CC[C@@]4(O3)CCOC4=O)(CCCC2(C)C)C)OC(=O)C
InChI InChI=1S/C22H34O5/c1-14-13-16(26-15(2)23)17-19(3,4)7-6-8-20(17,5)22(14)10-9-21(27-22)11-12-25-18(21)24/h14,16-17H,6-13H2,1-5H3/t14-,16+,17+,20-,21-,22-/m1/s1
InChI Key OVICILMSQORLAX-KCSQECINSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O5
Molecular Weight 378.50 g/mol
Exact Mass 378.24062418 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162821194

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 + 0.6479 64.79%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8022 80.22%
OATP2B1 inhibitior - 0.8664 86.64%
OATP1B1 inhibitior + 0.8871 88.71%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7125 71.25%
P-glycoprotein inhibitior - 0.4848 48.48%
P-glycoprotein substrate - 0.7034 70.34%
CYP3A4 substrate + 0.6599 65.99%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.8581 85.81%
CYP3A4 inhibition - 0.8955 89.55%
CYP2C9 inhibition - 0.7110 71.10%
CYP2C19 inhibition - 0.7546 75.46%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.9189 91.89%
CYP2C8 inhibition - 0.6536 65.36%
CYP inhibitory promiscuity - 0.9379 93.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5642 56.42%
Eye corrosion - 0.9785 97.85%
Eye irritation - 0.8642 86.42%
Skin irritation - 0.8023 80.23%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4163 41.63%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5773 57.73%
skin sensitisation - 0.8771 87.71%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7303 73.03%
Acute Oral Toxicity (c) III 0.6411 64.11%
Estrogen receptor binding + 0.8832 88.32%
Androgen receptor binding + 0.7035 70.35%
Thyroid receptor binding + 0.7386 73.86%
Glucocorticoid receptor binding + 0.8797 87.97%
Aromatase binding + 0.7962 79.62%
PPAR gamma - 0.4892 48.92%
Honey bee toxicity - 0.8318 83.18%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9734 97.34%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.57% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.04% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.86% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.26% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.65% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 87.66% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.85% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 86.82% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.29% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.99% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.23% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.89% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.71% 82.69%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.30% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.24% 99.23%
CHEMBL2581 P07339 Cathepsin D 82.12% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.06% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.87% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.58% 91.07%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.16% 90.08%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 80.84% 95.71%

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 trifolia

Cross-Links

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PubChem 162821194
LOTUS LTS0007174
wikiData Q105200745