(6E,8E)-4,6,8-Megastigmatriene

Details

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Internal ID e021da3e-3021-4fda-878e-9f7ab94bbe37
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (6Z)-6-[(E)-but-2-enylidene]-1,5,5-trimethylcyclohexene
SMILES (Canonical) CC=CC=C1C(=CCCC1(C)C)C
SMILES (Isomeric) C/C=C/C=C/1\C(=CCCC1(C)C)C
InChI InChI=1S/C13H20/c1-5-6-9-12-11(2)8-7-10-13(12,3)4/h5-6,8-9H,7,10H2,1-4H3/b6-5+,12-9+
InChI Key BYDQKMZEOZVIJM-HFACTSAFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20
Molecular Weight 176.30 g/mol
Exact Mass 176.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Megastigme-4,6(E),8(E)-triene
4,6,8-Megastigmatriene
Megastigma-4,6(E),8(Z)-triene
C13-H20
BYDQKMZEOZVIJM-HFACTSAFSA-N
CHEBI:184203
(6Z)-6-[(E)-but-2-enylidene]-1,5,5-trimethylcyclohexene
Cyclohexene, 6-(2-butenylidene)-1,5,5-trimethyl-, (E,Z)-
Megastigma-4,6(E),8(E)-triene
(6Z,8E)-Megastigma-4,6,8-triene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (6E,8E)-4,6,8-Megastigmatriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.9471 94.71%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.6177 61.77%
OATP2B1 inhibitior - 0.8654 86.54%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior - 0.3531 35.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7334 73.34%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.9400 94.00%
CYP3A4 substrate - 0.5778 57.78%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9129 91.29%
CYP2C9 inhibition - 0.9053 90.53%
CYP2C19 inhibition - 0.8817 88.17%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.8622 86.22%
CYP2C8 inhibition - 0.8537 85.37%
CYP inhibitory promiscuity - 0.6482 64.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Warning 0.5038 50.38%
Eye corrosion - 0.8231 82.31%
Eye irritation + 0.8582 85.82%
Skin irritation + 0.7528 75.28%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6071 60.71%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6428 64.28%
skin sensitisation + 0.9285 92.85%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6766 67.66%
Nephrotoxicity - 0.5767 57.67%
Acute Oral Toxicity (c) III 0.8810 88.10%
Estrogen receptor binding - 0.9645 96.45%
Androgen receptor binding - 0.8532 85.32%
Thyroid receptor binding - 0.8209 82.09%
Glucocorticoid receptor binding - 0.8833 88.33%
Aromatase binding - 0.9194 91.94%
PPAR gamma - 0.8554 85.54%
Honey bee toxicity - 0.9253 92.53%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9890 98.90%

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
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.98% 85.30%
CHEMBL2039 P27338 Monoamine oxidase B 90.31% 92.51%
CHEMBL1937 Q92769 Histone deacetylase 2 87.36% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.06% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.84% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.07% 96.09%

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.
Crocus sativus

Cross-Links

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PubChem 5369483
NPASS NPC75080