3-Methylidene-2-propan-2-ylcyclohexan-1-ol

Details

Top
Internal ID 2e3cb564-871e-4844-bfcb-303a474c27cf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 3-methylidene-2-propan-2-ylcyclohexan-1-ol
SMILES (Canonical) CC(C)C1C(CCCC1=C)O
SMILES (Isomeric) CC(C)C1C(CCCC1=C)O
InChI InChI=1S/C10H18O/c1-7(2)10-8(3)5-4-6-9(10)11/h7,9-11H,3-6H2,1-2H3
InChI Key GKJOISDJSXXEFB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-Methylidene-2-propan-2-ylcyclohexan-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.5352 53.52%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6209 62.09%
OATP2B1 inhibitior - 0.8448 84.48%
OATP1B1 inhibitior + 0.9332 93.32%
OATP1B3 inhibitior + 0.9342 93.42%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9640 96.40%
P-glycoprotein inhibitior - 0.9642 96.42%
P-glycoprotein substrate - 0.9385 93.85%
CYP3A4 substrate - 0.6510 65.10%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.9418 94.18%
CYP2C9 inhibition - 0.8960 89.60%
CYP2C19 inhibition - 0.8624 86.24%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.8873 88.73%
CYP2C8 inhibition - 0.9834 98.34%
CYP inhibitory promiscuity - 0.8407 84.07%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.6603 66.03%
Eye corrosion - 0.7255 72.55%
Eye irritation + 0.9355 93.55%
Skin irritation + 0.6190 61.90%
Skin corrosion - 0.8783 87.83%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6045 60.45%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6959 69.59%
skin sensitisation + 0.8279 82.79%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7342 73.42%
Acute Oral Toxicity (c) III 0.7929 79.29%
Estrogen receptor binding - 0.9033 90.33%
Androgen receptor binding - 0.8445 84.45%
Thyroid receptor binding - 0.8176 81.76%
Glucocorticoid receptor binding - 0.7170 71.70%
Aromatase binding - 0.8467 84.67%
PPAR gamma - 0.8626 86.26%
Honey bee toxicity - 0.9621 96.21%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8508 85.08%

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 90.67% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.09% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.42% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.98% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.72% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 82.29% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.03% 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.
Xylopia aromatica

Cross-Links

Top
PubChem 130149091
LOTUS LTS0156488
wikiData Q105010052