1,5,5-Trimethyl-6-(4-methylcyclohex-3-en-1-yl)cyclohexene

Details

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Internal ID b27b75ef-71ca-4a21-9616-59f4aa4a0a0d
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,5,5-trimethyl-6-(4-methylcyclohex-3-en-1-yl)cyclohexene
SMILES (Canonical) CC1=CCC(CC1)C2C(=CCCC2(C)C)C
SMILES (Isomeric) CC1=CCC(CC1)C2C(=CCCC2(C)C)C
InChI InChI=1S/C16H26/c1-12-7-9-14(10-8-12)15-13(2)6-5-11-16(15,3)4/h6-7,14-15H,5,8-11H2,1-4H3
InChI Key ITCITDAEAKLVHK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H26
Molecular Weight 218.38 g/mol
Exact Mass 218.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.12
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,5,5-Trimethyl-6-(4-methylcyclohex-3-en-1-yl)cyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.9584 95.84%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4056 40.56%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9519 95.19%
OATP1B3 inhibitior - 0.3382 33.82%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7278 72.78%
P-glycoprotein inhibitior - 0.9473 94.73%
P-glycoprotein substrate - 0.8748 87.48%
CYP3A4 substrate + 0.5460 54.60%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7640 76.40%
CYP3A4 inhibition - 0.9348 93.48%
CYP2C9 inhibition - 0.8598 85.98%
CYP2C19 inhibition - 0.7937 79.37%
CYP2D6 inhibition - 0.9589 95.89%
CYP1A2 inhibition - 0.8910 89.10%
CYP2C8 inhibition - 0.5840 58.40%
CYP inhibitory promiscuity + 0.5527 55.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4785 47.85%
Eye corrosion - 0.9247 92.47%
Eye irritation - 0.5986 59.86%
Skin irritation - 0.7201 72.01%
Skin corrosion - 0.9832 98.32%
Ames mutagenesis - 0.6523 65.23%
Human Ether-a-go-go-Related Gene inhibition + 0.7885 78.85%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5969 59.69%
skin sensitisation + 0.7888 78.88%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5626 56.26%
Acute Oral Toxicity (c) III 0.6276 62.76%
Estrogen receptor binding - 0.8516 85.16%
Androgen receptor binding - 0.5616 56.16%
Thyroid receptor binding - 0.7177 71.77%
Glucocorticoid receptor binding - 0.8128 81.28%
Aromatase binding - 0.8380 83.80%
PPAR gamma - 0.6009 60.09%
Honey bee toxicity - 0.8552 85.52%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 1.0000 100.00%

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 91.57% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.99% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.88% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.34% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.71% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.63% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.73% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.30% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.76% 90.17%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.45% 86.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.34% 93.99%
CHEMBL1871 P10275 Androgen Receptor 82.32% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.22% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 80.71% 89.05%

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.
Angelica sinensis
Atractylodes lancea

Cross-Links

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PubChem 5315803
NPASS NPC82098