Cyclopentaneethanol, beta,2,3-trimethyl-

Details

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Internal ID f0e04898-3798-410f-bd81-b487165d3970
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 2-(2,3-dimethylcyclopentyl)propan-1-ol
SMILES (Canonical) CC1CCC(C1C)C(C)CO
SMILES (Isomeric) CC1CCC(C1C)C(C)CO
InChI InChI=1S/C10H20O/c1-7-4-5-10(9(7)3)8(2)6-11/h7-11H,4-6H2,1-3H3
InChI Key OWKCKKNIZCLWKT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O
Molecular Weight 156.26 g/mol
Exact Mass 156.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2-(2,3-Dimethylcyclopentyl)-1-propanol #
Cyclopentaneethanol, .beta.,2,3-trimethyl-

2D Structure

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2D Structure of Cyclopentaneethanol, beta,2,3-trimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9839 98.39%
Caco-2 + 0.6818 68.18%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.7490 74.90%
OATP2B1 inhibitior - 0.8426 84.26%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9219 92.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9592 95.92%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.8644 86.44%
CYP3A4 substrate - 0.6461 64.61%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9031 90.31%
CYP2C9 inhibition - 0.8473 84.73%
CYP2C19 inhibition - 0.8907 89.07%
CYP2D6 inhibition - 0.9242 92.42%
CYP1A2 inhibition - 0.7857 78.57%
CYP2C8 inhibition - 0.9736 97.36%
CYP inhibitory promiscuity - 0.8599 85.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6534 65.34%
Eye corrosion + 0.6186 61.86%
Eye irritation + 0.8199 81.99%
Skin irritation - 0.5548 55.48%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6547 65.47%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6193 61.93%
skin sensitisation + 0.7968 79.68%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6145 61.45%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6356 63.56%
Acute Oral Toxicity (c) III 0.7423 74.23%
Estrogen receptor binding - 0.9044 90.44%
Androgen receptor binding - 0.6243 62.43%
Thyroid receptor binding - 0.7938 79.38%
Glucocorticoid receptor binding - 0.8711 87.11%
Aromatase binding - 0.8441 84.41%
PPAR gamma - 0.9182 91.82%
Honey bee toxicity - 0.9671 96.71%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9179 91.79%

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 95.11% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.49% 97.25%
CHEMBL2581 P07339 Cathepsin D 86.79% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.61% 97.09%
CHEMBL4072 P07858 Cathepsin B 84.16% 93.67%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.74% 96.47%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.94% 97.23%
CHEMBL3837 P07711 Cathepsin L 81.32% 96.61%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 549899
NPASS NPC305531