CID 163190142

Details

Top
Internal ID 630dfae7-06e9-4f7b-a479-8ab86f79385f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical) CCCCOC1C2(CCC3(O2)C(CC(C4C3(CCCC4(C)C)C)OC(=O)C)C)CC(=O)O1
SMILES (Isomeric) CCCCO[C@@H]1[C@@]2(CC[C@]3(O2)[C@H](C[C@@H]([C@H]4[C@]3(CCCC4(C)C)C)OC(=O)C)C)CC(=O)O1
InChI InChI=1S/C26H42O6/c1-7-8-14-29-22-25(16-20(28)31-22)12-13-26(32-25)17(2)15-19(30-18(3)27)21-23(4,5)10-9-11-24(21,26)6/h17,19,21-22H,7-16H2,1-6H3/t17-,19-,21+,22-,24+,25+,26-/m0/s1
InChI Key CFJIARCTYBJYBE-VZTUBQQKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H42O6
Molecular Weight 450.60 g/mol
Exact Mass 450.29813906 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.17
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 163190142

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.5318 53.18%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7737 77.37%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.7720 77.20%
OATP1B3 inhibitior + 0.9506 95.06%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.7195 71.95%
P-glycoprotein inhibitior + 0.6811 68.11%
P-glycoprotein substrate + 0.5121 51.21%
CYP3A4 substrate + 0.7097 70.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8625 86.25%
CYP3A4 inhibition - 0.8097 80.97%
CYP2C9 inhibition - 0.6159 61.59%
CYP2C19 inhibition - 0.6547 65.47%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition - 0.9273 92.73%
CYP2C8 inhibition + 0.6607 66.07%
CYP inhibitory promiscuity - 0.8292 82.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5698 56.98%
Eye corrosion - 0.9814 98.14%
Eye irritation - 0.8871 88.71%
Skin irritation - 0.7973 79.73%
Skin corrosion - 0.9385 93.85%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4232 42.32%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.5275 52.75%
skin sensitisation - 0.8911 89.11%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6865 68.65%
Acute Oral Toxicity (c) III 0.7147 71.47%
Estrogen receptor binding + 0.7923 79.23%
Androgen receptor binding + 0.6926 69.26%
Thyroid receptor binding + 0.6631 66.31%
Glucocorticoid receptor binding + 0.7389 73.89%
Aromatase binding + 0.7234 72.34%
PPAR gamma + 0.6539 65.39%
Honey bee toxicity - 0.8637 86.37%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9840 98.40%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.84% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.89% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.13% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 95.90% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.62% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.05% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.16% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.89% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 86.49% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.43% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.98% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 83.29% 91.49%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.23% 95.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.20% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.26% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.98% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.74% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.56% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.55% 89.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.23% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.00% 100.00%

Plants that contains it

Top
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

Top
PubChem 163190142
LOTUS LTS0228151
wikiData Q104956643