1,1,3-Trimethylcyclohexan

Details

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Internal ID 5e64c3b1-d97d-4fa6-aacb-b04a9b3f5eff
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name (3S)-1,1,3-trimethylcyclohexane
SMILES (Canonical) CC1CCCC(C1)(C)C
SMILES (Isomeric) C[C@H]1CCCC(C1)(C)C
InChI InChI=1S/C9H18/c1-8-5-4-6-9(2,3)7-8/h8H,4-7H2,1-3H3/t8-/m0/s1
InChI Key PYOLJOJPIPCRDP-QMMMGPOBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18
Molecular Weight 126.24 g/mol
Exact Mass 126.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,1,3-Trimethylcyclohexan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.8572 85.72%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.6991 69.91%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.9307 93.07%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9447 94.47%
P-glycoprotein inhibitior - 0.9798 97.98%
P-glycoprotein substrate - 0.9662 96.62%
CYP3A4 substrate - 0.5735 57.35%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.7671 76.71%
CYP3A4 inhibition - 0.9547 95.47%
CYP2C9 inhibition - 0.9116 91.16%
CYP2C19 inhibition - 0.9537 95.37%
CYP2D6 inhibition - 0.9610 96.10%
CYP1A2 inhibition - 0.9140 91.40%
CYP2C8 inhibition - 0.9712 97.12%
CYP inhibitory promiscuity - 0.9283 92.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5226 52.26%
Eye corrosion + 0.9149 91.49%
Eye irritation + 0.9822 98.22%
Skin irritation + 0.6867 68.67%
Skin corrosion - 0.9804 98.04%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6890 68.90%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5397 53.97%
skin sensitisation + 0.8908 89.08%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity + 0.5869 58.69%
Nephrotoxicity - 0.5554 55.54%
Acute Oral Toxicity (c) IV 0.6567 65.67%
Estrogen receptor binding - 0.9051 90.51%
Androgen receptor binding - 0.8738 87.38%
Thyroid receptor binding - 0.8555 85.55%
Glucocorticoid receptor binding - 0.9152 91.52%
Aromatase binding - 0.9074 90.74%
PPAR gamma - 0.9199 91.99%
Honey bee toxicity - 0.8936 89.36%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8200 82.00%
Fish aquatic toxicity + 0.9874 98.74%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.25% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.42% 97.09%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 88.41% 95.27%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.21% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.94% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.97% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.86% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.21% 100.00%
CHEMBL259 P32245 Melanocortin receptor 4 82.92% 95.38%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.15% 86.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.64% 82.69%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.45% 99.18%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.40% 94.78%
CHEMBL3012 Q13946 Phosphodiesterase 7A 80.31% 99.29%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.24% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.20% 95.50%

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.
Passiflora edulis

Cross-Links

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PubChem 57176118
LOTUS LTS0246493
wikiData Q105216679