1,4-Cyclohexadiene

Details

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Internal ID b6d404cd-6992-4469-9dcc-f78be4e2f1e2
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins
IUPAC Name cyclohexa-1,4-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2
InChI Key UVJHQYIOXKWHFD-UHFFFAOYSA-N
Popularity 862 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8
Molecular Weight 80.13 g/mol
Exact Mass 80.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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628-41-1
Cyclohexa-1,4-diene
0F8Z5909QZ
DTXSID0060854
CHEBI:37611
RefChem:73171
DTXCID6043547
211-043-1
1,4-Dihydrobenzene
1,4-Cyclohexanediene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,4-Cyclohexadiene

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 + 0.9200 92.00%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.4279 42.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9821 98.21%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9162 91.62%
P-glycoprotein inhibitior - 0.9875 98.75%
P-glycoprotein substrate - 0.9960 99.60%
CYP3A4 substrate - 0.8481 84.81%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7346 73.46%
CYP3A4 inhibition - 0.9380 93.80%
CYP2C9 inhibition - 0.9020 90.20%
CYP2C19 inhibition - 0.9251 92.51%
CYP2D6 inhibition - 0.9652 96.52%
CYP1A2 inhibition - 0.7001 70.01%
CYP2C8 inhibition - 0.9962 99.62%
CYP inhibitory promiscuity - 0.6511 65.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5764 57.64%
Carcinogenicity (trinary) Warning 0.5539 55.39%
Eye corrosion + 0.9967 99.67%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9537 95.37%
Skin corrosion + 0.6451 64.51%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7914 79.14%
Micronuclear - 0.8841 88.41%
Hepatotoxicity + 0.8993 89.93%
skin sensitisation + 0.9524 95.24%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6363 63.63%
Acute Oral Toxicity (c) III 0.6811 68.11%
Estrogen receptor binding - 0.9545 95.45%
Androgen receptor binding - 0.9401 94.01%
Thyroid receptor binding - 0.8873 88.73%
Glucocorticoid receptor binding - 0.8697 86.97%
Aromatase binding - 0.8948 89.48%
PPAR gamma - 0.8266 82.66%
Honey bee toxicity - 0.8527 85.27%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9415 94.15%

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
No predicted targets yet!

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.
Forsythia suspensa
Forsythia viridissima

Cross-Links

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PubChem 12343
NPASS NPC296108