CID 6711881

Details

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Internal ID 4fae9fd6-68e0-4fa2-87ee-93c626ffe898
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC1C(=O)CC2C(CCCC2(C13CCC4(O3)COC=C4)C)(C)C
SMILES (Isomeric) C[C@@H]1C(=O)CC2[C@@]([C@@]13CC[C@]4(O3)COC=C4)(CCCC2(C)C)C
InChI InChI=1S/C20H30O3/c1-14-15(21)12-16-17(2,3)6-5-7-18(16,4)20(14)9-8-19(23-20)10-11-22-13-19/h10-11,14,16H,5-9,12-13H2,1-4H3/t14-,16?,18+,19-,20-/m1/s1
InChI Key MFAYXOLUJJXHCN-YEJLTRTHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O3
Molecular Weight 318.40 g/mol
Exact Mass 318.21949481 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CHEMBL1982919
NSC-645754
NCI60_015678

2D Structure

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2D Structure of CID 6711881

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7632 76.32%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7333 73.33%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8496 84.96%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.5125 51.25%
P-glycoprotein inhibitior - 0.7283 72.83%
P-glycoprotein substrate - 0.8120 81.20%
CYP3A4 substrate + 0.5866 58.66%
CYP2C9 substrate - 0.7917 79.17%
CYP2D6 substrate - 0.8100 81.00%
CYP3A4 inhibition - 0.9087 90.87%
CYP2C9 inhibition - 0.8739 87.39%
CYP2C19 inhibition - 0.7774 77.74%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition - 0.7334 73.34%
CYP2C8 inhibition - 0.6632 66.32%
CYP inhibitory promiscuity - 0.8804 88.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5138 51.38%
Eye corrosion - 0.9836 98.36%
Eye irritation - 0.8989 89.89%
Skin irritation - 0.7000 70.00%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.5370 53.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6559 65.59%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation - 0.7164 71.64%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5474 54.74%
Acute Oral Toxicity (c) III 0.6412 64.12%
Estrogen receptor binding + 0.8238 82.38%
Androgen receptor binding + 0.6599 65.99%
Thyroid receptor binding + 0.6919 69.19%
Glucocorticoid receptor binding + 0.6493 64.93%
Aromatase binding + 0.7277 72.77%
PPAR gamma + 0.5923 59.23%
Honey bee toxicity - 0.8487 84.87%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9737 97.37%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.46% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.90% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.36% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.62% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.85% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 87.46% 86.00%
CHEMBL2581 P07339 Cathepsin D 87.32% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.71% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.17% 96.77%
CHEMBL325 Q13547 Histone deacetylase 1 86.12% 95.92%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.91% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.43% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.92% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.55% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.64% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.56% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.39% 95.89%

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.
Leonurus japonicus
Schisandra chinensis

Cross-Links

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PubChem 6711881
NPASS NPC214292
LOTUS LTS0089408
wikiData Q104402346