(S)-9,10-Cyclo-p-menth-1-en-4-ol

Details

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Internal ID 9af75638-eee3-436a-ba31-0ac8c4951991
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 1-cyclopropyl-4-methylcyclohex-3-en-1-ol
SMILES (Canonical) CC1=CCC(CC1)(C2CC2)O
SMILES (Isomeric) CC1=CCC(CC1)(C2CC2)O
InChI InChI=1S/C10H16O/c1-8-4-6-10(11,7-5-8)9-2-3-9/h4,9,11H,2-3,5-7H2,1H3
InChI Key FTEUSHRMTWTVTP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEBI:171958
9,10-Cyclo-p-menth-1-en-4-ol
1-cyclopropyl-4-methylcyclohex-3-en-1-ol

2D Structure

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2D Structure of (S)-9,10-Cyclo-p-menth-1-en-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8303 83.03%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6584 65.84%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.9641 96.41%
OATP1B3 inhibitior + 0.9568 95.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8922 89.22%
P-glycoprotein inhibitior - 0.9822 98.22%
P-glycoprotein substrate - 0.9243 92.43%
CYP3A4 substrate - 0.5689 56.89%
CYP2C9 substrate - 0.5790 57.90%
CYP2D6 substrate - 0.7630 76.30%
CYP3A4 inhibition - 0.9474 94.74%
CYP2C9 inhibition - 0.8129 81.29%
CYP2C19 inhibition - 0.7831 78.31%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.7776 77.76%
CYP2C8 inhibition - 0.9226 92.26%
CYP inhibitory promiscuity - 0.8646 86.46%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.5465 54.65%
Eye corrosion - 0.8841 88.41%
Eye irritation + 0.9558 95.58%
Skin irritation + 0.6807 68.07%
Skin corrosion - 0.9271 92.71%
Ames mutagenesis - 0.9170 91.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7264 72.64%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5972 59.72%
skin sensitisation + 0.6774 67.74%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6917 69.17%
Acute Oral Toxicity (c) III 0.7303 73.03%
Estrogen receptor binding - 0.9389 93.89%
Androgen receptor binding - 0.8339 83.39%
Thyroid receptor binding - 0.8185 81.85%
Glucocorticoid receptor binding - 0.7742 77.42%
Aromatase binding - 0.9021 90.21%
PPAR gamma - 0.8182 81.82%
Honey bee toxicity - 0.9449 94.49%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5200 52.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.55% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.00% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.79% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.19% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.93% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.30% 97.25%
CHEMBL4208 P20618 Proteasome component C5 82.61% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.15% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.81% 95.56%

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.
Pistacia vera

Cross-Links

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PubChem 73815132
LOTUS LTS0231743
wikiData Q105001016