1,3-Divinylbenzene

Details

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Internal ID 4235461b-91de-4965-85a0-7ea0d2868f3d
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 1,3-bis(ethenyl)benzene
SMILES (Canonical) C=CC1=CC(=CC=C1)C=C
SMILES (Isomeric) C=CC1=CC(=CC=C1)C=C
InChI InChI=1S/C10H10/c1-3-9-6-5-7-10(4-2)8-9/h3-8H,1-2H2
InChI Key PRJNEUBECVAVAG-UHFFFAOYSA-N
Popularity 64 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10
Molecular Weight 130.19 g/mol
Exact Mass 130.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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108-57-6
m-Divinylbenzene
1,3-Diethenylbenzene
Benzene, 1,3-diethenyl-
m-Vinylstyrene
1,3-bis(ethenyl)benzene
Benzene, m-divinyl-
m-Divinylbenzen
m-Divinylbenzen [Czech]
m-Divinyl benzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3-Divinylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9543 95.43%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4285 42.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9590 95.90%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9094 90.94%
P-glycoprotein inhibitior - 0.9795 97.95%
P-glycoprotein substrate - 0.9875 98.75%
CYP3A4 substrate - 0.7967 79.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7136 71.36%
CYP3A4 inhibition - 0.9332 93.32%
CYP2C9 inhibition - 0.9089 90.89%
CYP2C19 inhibition - 0.8449 84.49%
CYP2D6 inhibition - 0.9538 95.38%
CYP1A2 inhibition - 0.6715 67.15%
CYP2C8 inhibition - 0.9210 92.10%
CYP inhibitory promiscuity - 0.6502 65.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5864 58.64%
Carcinogenicity (trinary) Warning 0.5426 54.26%
Eye corrosion + 1.0000 100.00%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9514 95.14%
Skin corrosion - 0.5284 52.84%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7490 74.90%
Micronuclear - 0.9641 96.41%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.9868 98.68%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.6776 67.76%
Acute Oral Toxicity (c) III 0.8054 80.54%
Estrogen receptor binding - 0.7522 75.22%
Androgen receptor binding - 0.8104 81.04%
Thyroid receptor binding - 0.7557 75.57%
Glucocorticoid receptor binding - 0.8650 86.50%
Aromatase binding - 0.8162 81.62%
PPAR gamma - 0.7632 76.32%
Honey bee toxicity - 0.8568 85.68%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9771 97.71%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.49% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.09% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.57% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 86.72% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 85.20% 94.73%
CHEMBL2581 P07339 Cathepsin D 85.10% 98.95%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 82.32% 96.42%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.65% 96.00%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 80.26% 81.29%

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 7941
NPASS NPC176985