1,3,3-Trimethyl-2-(2-methyl-cyclopropyl)-cyclohexene

Details

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Internal ID 4dc06fbc-205f-4878-8c0b-d2e4b2e7dc75
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,3,3-trimethyl-2-(2-methylcyclopropyl)cyclohexene
SMILES (Canonical) CC1CC1C2=C(CCCC2(C)C)C
SMILES (Isomeric) CC1CC1C2=C(CCCC2(C)C)C
InChI InChI=1S/C13H22/c1-9-6-5-7-13(3,4)12(9)11-8-10(11)2/h10-11H,5-8H2,1-4H3
InChI Key BIJUQTKPTMHITN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22
Molecular Weight 178.31 g/mol
Exact Mass 178.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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BIJUQTKPTMHITN-UHFFFAOYSA-N
1,3,3-Trimethyl-2-(2-methylcyclopropyl)-1-cyclohexene #

2D Structure

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2D Structure of 1,3,3-Trimethyl-2-(2-methyl-cyclopropyl)-cyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.8653 86.53%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5128 51.28%
OATP2B1 inhibitior - 0.8452 84.52%
OATP1B1 inhibitior + 0.8770 87.70%
OATP1B3 inhibitior - 0.3198 31.98%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8166 81.66%
P-glycoprotein inhibitior - 0.9190 91.90%
P-glycoprotein substrate - 0.9544 95.44%
CYP3A4 substrate - 0.5225 52.25%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7640 76.40%
CYP3A4 inhibition - 0.9583 95.83%
CYP2C9 inhibition - 0.8746 87.46%
CYP2C19 inhibition - 0.8324 83.24%
CYP2D6 inhibition - 0.9529 95.29%
CYP1A2 inhibition - 0.8250 82.50%
CYP2C8 inhibition - 0.8357 83.57%
CYP inhibitory promiscuity - 0.6087 60.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.4631 46.31%
Eye corrosion - 0.9066 90.66%
Eye irritation + 0.8892 88.92%
Skin irritation + 0.5823 58.23%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.7987 79.87%
Human Ether-a-go-go-Related Gene inhibition - 0.5418 54.18%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation + 0.8427 84.27%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5074 50.74%
Nephrotoxicity - 0.6189 61.89%
Acute Oral Toxicity (c) III 0.6824 68.24%
Estrogen receptor binding - 0.9187 91.87%
Androgen receptor binding - 0.7096 70.96%
Thyroid receptor binding - 0.7529 75.29%
Glucocorticoid receptor binding - 0.8923 89.23%
Aromatase binding - 0.8045 80.45%
PPAR gamma - 0.8752 87.52%
Honey bee toxicity - 0.8363 83.63%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9960 99.60%

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 93.58% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.07% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.21% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.61% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.34% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.61% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.25% 100.00%
CHEMBL230 P35354 Cyclooxygenase-2 83.19% 89.63%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 80.02% 90.71%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 595941
NPASS NPC190693