Conocenol A

Details

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Internal ID cf13cd7a-4a44-4271-a2c3-d22234633981
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name [(2R,5S,8S,8aS)-2,4-bis(hydroxymethyl)-2,8-dimethyl-3,5,6,7,8,8a-hexahydro-1H-azulen-5-yl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O3/c1-10-3-4-11(7-16)14(8-17)13-6-15(2,9-18)5-12(10)13/h10-12,16-18H,3-9H2,1-2H3/t10-,11+,12-,15+/m0/s1
InChI Key OVEMDSHJDSVUAE-OZTPJHRESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Conocenol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 + 0.5704 57.04%
Blood Brain Barrier + 0.7493 74.93%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6468 64.68%
OATP2B1 inhibitior - 0.8474 84.74%
OATP1B1 inhibitior + 0.9073 90.73%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6876 68.76%
BSEP inhibitior - 0.9121 91.21%
P-glycoprotein inhibitior - 0.9156 91.56%
P-glycoprotein substrate - 0.7506 75.06%
CYP3A4 substrate + 0.5291 52.91%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.8449 84.49%
CYP2C9 inhibition - 0.7478 74.78%
CYP2C19 inhibition - 0.7941 79.41%
CYP2D6 inhibition - 0.8879 88.79%
CYP1A2 inhibition - 0.7368 73.68%
CYP2C8 inhibition - 0.6236 62.36%
CYP inhibitory promiscuity - 0.7792 77.92%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5966 59.66%
Eye corrosion - 0.9598 95.98%
Eye irritation + 0.6712 67.12%
Skin irritation - 0.7724 77.24%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5086 50.86%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6256 62.56%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.6919 69.19%
Acute Oral Toxicity (c) III 0.5579 55.79%
Estrogen receptor binding - 0.4856 48.56%
Androgen receptor binding - 0.5628 56.28%
Thyroid receptor binding - 0.5523 55.23%
Glucocorticoid receptor binding - 0.5222 52.22%
Aromatase binding - 0.6998 69.98%
PPAR gamma - 0.8146 81.46%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9849 98.49%

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 97.38% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.29% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.89% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.12% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 92.91% 95.93%
CHEMBL2996 Q05655 Protein kinase C delta 86.21% 97.79%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.33% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.12% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.70% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 80.79% 90.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 23643842
LOTUS LTS0109521
wikiData Q77561579