CID 162923730

Details

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Internal ID 688bc61d-8c04-4b2e-a77e-0e77c8bb658a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CCOC1CC2(CCC3(O2)C(C(=O)C(C4C3(CCCC4(C)C)C)C)C)CO1
SMILES (Isomeric) CCOC1CC2(CCC3(O2)C(C(=O)C(C4C3(CCCC4(C)C)C)C)C)CO1
InChI InChI=1S/C23H38O4/c1-7-25-17-13-22(14-26-17)11-12-23(27-22)16(3)18(24)15(2)19-20(4,5)9-8-10-21(19,23)6/h15-17,19H,7-14H2,1-6H3
InChI Key PIERVVMAODGPOO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H38O4
Molecular Weight 378.50 g/mol
Exact Mass 378.27700969 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.74
H-Bond Acceptor 4
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 162923730

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9870 98.70%
Caco-2 + 0.7216 72.16%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6967 69.67%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.8593 85.93%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.5657 56.57%
P-glycoprotein inhibitior - 0.5953 59.53%
P-glycoprotein substrate - 0.6836 68.36%
CYP3A4 substrate + 0.6660 66.60%
CYP2C9 substrate - 0.8103 81.03%
CYP2D6 substrate - 0.8421 84.21%
CYP3A4 inhibition - 0.8354 83.54%
CYP2C9 inhibition - 0.7493 74.93%
CYP2C19 inhibition - 0.5880 58.80%
CYP2D6 inhibition - 0.9293 92.93%
CYP1A2 inhibition - 0.9134 91.34%
CYP2C8 inhibition - 0.6218 62.18%
CYP inhibitory promiscuity - 0.8149 81.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5338 53.38%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8303 83.03%
Skin irritation - 0.7876 78.76%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis + 0.5036 50.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4950 49.50%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.6433 64.33%
skin sensitisation - 0.8915 89.15%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.8407 84.07%
Acute Oral Toxicity (c) III 0.6003 60.03%
Estrogen receptor binding + 0.9281 92.81%
Androgen receptor binding + 0.7181 71.81%
Thyroid receptor binding + 0.6776 67.76%
Glucocorticoid receptor binding + 0.7919 79.19%
Aromatase binding + 0.8117 81.17%
PPAR gamma + 0.6177 61.77%
Honey bee toxicity - 0.7829 78.29%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9821 98.21%

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 92.64% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.58% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.37% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.64% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.36% 96.77%
CHEMBL2581 P07339 Cathepsin D 89.42% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.38% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 88.79% 94.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 87.47% 95.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.67% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.84% 100.00%
CHEMBL5555 O00767 Acyl-CoA desaturase 84.37% 97.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.69% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.97% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.56% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.03% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.80% 82.69%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.23% 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.
Pseudodictamnus aucheri

Cross-Links

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PubChem 162923730
LOTUS LTS0174200
wikiData Q105209468