2-Methyl-5-propan-2-ylcyclohexa-1,5-dien-1-ol

Details

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Internal ID 92ebd51c-e9d5-48f0-a32e-10b919db668f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-methyl-5-propan-2-ylcyclohexa-1,5-dien-1-ol
SMILES (Canonical) CC1=C(C=C(CC1)C(C)C)O
SMILES (Isomeric) CC1=C(C=C(CC1)C(C)C)O
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h6-7,11H,4-5H2,1-3H3
InChI Key WINXWCKAWOVXQI-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 2.10
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-5-propan-2-ylcyclohexa-1,5-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.7988 79.88%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4533 45.33%
OATP2B1 inhibitior - 0.8421 84.21%
OATP1B1 inhibitior + 0.8935 89.35%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9513 95.13%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.9431 94.31%
CYP3A4 substrate - 0.6826 68.26%
CYP2C9 substrate + 0.6075 60.75%
CYP2D6 substrate - 0.8126 81.26%
CYP3A4 inhibition - 0.8710 87.10%
CYP2C9 inhibition - 0.7853 78.53%
CYP2C19 inhibition - 0.7887 78.87%
CYP2D6 inhibition - 0.8693 86.93%
CYP1A2 inhibition - 0.6591 65.91%
CYP2C8 inhibition - 0.9791 97.91%
CYP inhibitory promiscuity - 0.6579 65.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6124 61.24%
Eye corrosion - 0.8028 80.28%
Eye irritation + 0.9389 93.89%
Skin irritation + 0.8004 80.04%
Skin corrosion - 0.5990 59.90%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5743 57.43%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.8348 83.48%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6786 67.86%
Acute Oral Toxicity (c) III 0.7298 72.98%
Estrogen receptor binding - 0.9553 95.53%
Androgen receptor binding - 0.7062 70.62%
Thyroid receptor binding - 0.7880 78.80%
Glucocorticoid receptor binding - 0.8329 83.29%
Aromatase binding - 0.9082 90.82%
PPAR gamma - 0.8518 85.18%
Honey bee toxicity - 0.9553 95.53%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9570 95.70%

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
CHEMBL2581 P07339 Cathepsin D 90.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.00% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.94% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.89% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.31% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.96% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.86% 93.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.05% 99.15%

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.
Xylopia aromatica

Cross-Links

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PubChem 13670329
LOTUS LTS0135362
wikiData Q105306391