4beta-tert-Butyl-2-cyclohexen-1beta-ol

Details

Top
Internal ID a5bdf727-296a-434b-8361-a8c089dc097d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name (1R,4S)-4-tert-butylcyclohex-2-en-1-ol
SMILES (Canonical) CC(C)(C)C1CCC(C=C1)O
SMILES (Isomeric) CC(C)(C)[C@H]1CC[C@H](C=C1)O
InChI InChI=1S/C10H18O/c1-10(2,3)8-4-6-9(11)7-5-8/h4,6,8-9,11H,5,7H2,1-3H3/t8-,9+/m1/s1
InChI Key NGXNAIZTJAUMGV-BDAKNGLRSA-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 2.50
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
NGXNAIZTJAUMGV-BDAKNGLRSA-N
4beta-tert-Butyl-2-cyclohexen-1beta-ol

2D Structure

Top
2D Structure of 4beta-tert-Butyl-2-cyclohexen-1beta-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.6969 69.69%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5004 50.04%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9585 95.85%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9586 95.86%
P-glycoprotein inhibitior - 0.9815 98.15%
P-glycoprotein substrate - 0.9438 94.38%
CYP3A4 substrate - 0.6565 65.65%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.7466 74.66%
CYP3A4 inhibition - 0.9247 92.47%
CYP2C9 inhibition - 0.8714 87.14%
CYP2C19 inhibition - 0.8977 89.77%
CYP2D6 inhibition - 0.9436 94.36%
CYP1A2 inhibition - 0.8407 84.07%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.9434 94.34%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.6678 66.78%
Eye corrosion - 0.5772 57.72%
Eye irritation + 0.7759 77.59%
Skin irritation + 0.8575 85.75%
Skin corrosion - 0.7749 77.49%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5790 57.90%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8607 86.07%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8446 84.46%
Nephrotoxicity - 0.6093 60.93%
Acute Oral Toxicity (c) III 0.8682 86.82%
Estrogen receptor binding - 0.8706 87.06%
Androgen receptor binding - 0.9458 94.58%
Thyroid receptor binding - 0.7818 78.18%
Glucocorticoid receptor binding - 0.6844 68.44%
Aromatase binding - 0.9308 93.08%
PPAR gamma - 0.9154 91.54%
Honey bee toxicity - 0.8555 85.55%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.5586 55.86%

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 93.25% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.70% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.73% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 80.52% 98.95%

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.
Elettaria cardamomum
Ephedra sinica
Piper nigrum
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

Top
PubChem 6427100
NPASS NPC103700