4-Methyl-1,4-heptadiene

Details

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Internal ID ead0120c-b008-4b85-a049-7cbbc07a298b
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (4E)-4-methylhepta-1,4-diene
SMILES (Canonical) CCC=C(C)CC=C
SMILES (Isomeric) CC/C=C(\C)/CC=C
InChI InChI=1S/C8H14/c1-4-6-8(3)7-5-2/h4,7H,1,5-6H2,2-3H3/b8-7+
InChI Key NZXFAMRCCGUQGQ-BQYQJAHWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14
Molecular Weight 110.20 g/mol
Exact Mass 110.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1,4-Heptadiene, 4-methyl-
RefChem:1053332
4-Methyl-1,4-heptadiene
(4E)-4-methylhepta-1,4-diene
(4E)-4-Methyl-1,4-heptadiene
SCHEMBL1206451
SCHEMBL10442071
SCHEMBL14759568
CHEBI:229275
NZXFAMRCCGUQGQ-BQYQJAHWSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methyl-1,4-heptadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.9370 93.70%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5103 51.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9187 91.87%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9011 90.11%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9685 96.85%
CYP3A4 substrate - 0.6914 69.14%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9250 92.50%
CYP2C9 inhibition - 0.8924 89.24%
CYP2C19 inhibition - 0.8714 87.14%
CYP2D6 inhibition - 0.9017 90.17%
CYP1A2 inhibition - 0.6343 63.43%
CYP2C8 inhibition - 0.9400 94.00%
CYP inhibitory promiscuity - 0.6133 61.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6100 61.00%
Carcinogenicity (trinary) Warning 0.4922 49.22%
Eye corrosion + 0.7836 78.36%
Eye irritation + 0.9722 97.22%
Skin irritation + 0.7961 79.61%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7170 71.70%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.9366 93.66%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5892 58.92%
Acute Oral Toxicity (c) III 0.6250 62.50%
Estrogen receptor binding - 0.9628 96.28%
Androgen receptor binding - 0.9336 93.36%
Thyroid receptor binding - 0.9259 92.59%
Glucocorticoid receptor binding - 0.9399 93.99%
Aromatase binding - 0.9013 90.13%
PPAR gamma - 0.8859 88.59%
Honey bee toxicity - 0.8420 84.20%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9956 99.56%

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 86.45% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 85.85% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 82.55% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.01% 89.34%

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.
Ficus carica

Cross-Links

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PubChem 5362810
NPASS NPC253936