CID 75604483

Details

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Internal ID bc6087dd-ad94-4180-81ba-8d6e885648d8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical) CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4OC)C)(C)C)OC(=O)C
SMILES (Isomeric) CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4OC)C)(C)C)OC(=O)C
InChI InChI=1S/C23H36O6/c1-14-12-16(27-15(2)24)18-20(3,4)8-7-9-21(18,5)23(14)11-10-22(29-23)13-17(25)28-19(22)26-6/h14,16,18-19H,7-13H2,1-6H3
InChI Key SFOHMBBFSBTGGN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H36O6
Molecular Weight 408.50 g/mol
Exact Mass 408.25118886 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 6
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 75604483

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9828 98.28%
Caco-2 + 0.6017 60.17%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7434 74.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8014 80.14%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.4808 48.08%
P-glycoprotein inhibitior + 0.6520 65.20%
P-glycoprotein substrate - 0.6493 64.93%
CYP3A4 substrate + 0.6910 69.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8625 86.25%
CYP3A4 inhibition - 0.8540 85.40%
CYP2C9 inhibition - 0.8279 82.79%
CYP2C19 inhibition - 0.7708 77.08%
CYP2D6 inhibition - 0.9414 94.14%
CYP1A2 inhibition - 0.8960 89.60%
CYP2C8 inhibition + 0.4639 46.39%
CYP inhibitory promiscuity - 0.9613 96.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5769 57.69%
Eye corrosion - 0.9779 97.79%
Eye irritation - 0.8240 82.40%
Skin irritation - 0.7554 75.54%
Skin corrosion - 0.8742 87.42%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5185 51.85%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5708 57.08%
skin sensitisation - 0.8561 85.61%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.7503 75.03%
Acute Oral Toxicity (c) III 0.5925 59.25%
Estrogen receptor binding + 0.8176 81.76%
Androgen receptor binding + 0.6719 67.19%
Thyroid receptor binding + 0.7005 70.05%
Glucocorticoid receptor binding + 0.7127 71.27%
Aromatase binding + 0.7153 71.53%
PPAR gamma + 0.6538 65.38%
Honey bee toxicity - 0.6651 66.51%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9529 95.29%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.66% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.65% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 90.51% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.31% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.94% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.66% 85.14%
CHEMBL2996 Q05655 Protein kinase C delta 87.41% 97.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.28% 92.94%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.99% 91.07%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.77% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.91% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 84.10% 94.75%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.80% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.29% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.86% 89.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.23% 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 agnus-castus
Vitex trifolia subsp. litoralis

Cross-Links

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PubChem 75604483
LOTUS LTS0073465
wikiData Q105251907