Clovane, 2beta,9alpha-diol

Details

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Internal ID baab260d-8f40-4e6f-829b-0e7d90f480ad
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,4,8-trimethyltricyclo[6.3.1.01,5]dodecane-3,6-diol
SMILES (Canonical) CC1(C(CC23C1C(CC(C2)(CCC3)C)O)O)C
SMILES (Isomeric) CC1(C(CC23C1C(CC(C2)(CCC3)C)O)O)C
InChI InChI=1S/C15H26O2/c1-13(2)11(17)8-15-6-4-5-14(3,9-15)7-10(16)12(13)15/h10-12,16-17H,4-9H2,1-3H3
InChI Key XUAASKRYNOBPBG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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Clovane, 2.beta.,9.alpha.-diol

2D Structure

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2D Structure of Clovane, 2beta,9alpha-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.6706 67.06%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.4766 47.66%
OATP2B1 inhibitior - 0.8470 84.70%
OATP1B1 inhibitior + 0.9449 94.49%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8496 84.96%
P-glycoprotein inhibitior - 0.9491 94.91%
P-glycoprotein substrate - 0.8734 87.34%
CYP3A4 substrate + 0.5503 55.03%
CYP2C9 substrate - 0.5901 59.01%
CYP2D6 substrate - 0.6964 69.64%
CYP3A4 inhibition - 0.9351 93.51%
CYP2C9 inhibition - 0.8921 89.21%
CYP2C19 inhibition - 0.8959 89.59%
CYP2D6 inhibition - 0.9678 96.78%
CYP1A2 inhibition - 0.5229 52.29%
CYP2C8 inhibition - 0.9385 93.85%
CYP inhibitory promiscuity - 0.8743 87.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6108 61.08%
Eye corrosion - 0.9810 98.10%
Eye irritation + 0.5782 57.82%
Skin irritation + 0.6481 64.81%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.7654 76.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6586 65.86%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5319 53.19%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.4635 46.35%
Acute Oral Toxicity (c) III 0.8136 81.36%
Estrogen receptor binding - 0.5978 59.78%
Androgen receptor binding - 0.4912 49.12%
Thyroid receptor binding - 0.5366 53.66%
Glucocorticoid receptor binding - 0.5279 52.79%
Aromatase binding - 0.7131 71.31%
PPAR gamma - 0.8068 80.68%
Honey bee toxicity - 0.8645 86.45%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5711 57.11%
Fish aquatic toxicity + 0.9375 93.75%

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 91.91% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.19% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.92% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 85.99% 97.79%
CHEMBL259 P32245 Melanocortin receptor 4 85.30% 95.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.69% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 81.29% 95.93%

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.
Cinnamomum aromaticum
Saussurea cordifolia

Cross-Links

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PubChem 495838
NPASS NPC167960
LOTUS LTS0130082
wikiData Q105342033