1,2-Xylene; 1,3-xylene; 1,4-xylene

Details

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Internal ID c1248de5-3bd4-4d9d-8c10-2a1f0633c3c3
Taxonomy Benzenoids > Benzene and substituted derivatives > Xylenes > p-Xylenes
IUPAC Name 1,2-xylene;1,3-xylene;1,4-xylene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/3C8H10/c1-7-3-5-8(2)6-4-7;1-7-4-3-5-8(2)6-7;1-7-5-3-4-6-8(7)2/h3*3-6H,1-2H3
InChI Key MVZVDAGWAAZJPE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H30
Molecular Weight 318.50 g/mol
Exact Mass 318.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 6.91
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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RefChem:412235
905-215-1
1,2-xylene;1,3-xylene;1,4-xylene
Xylenen
Xylenes, ACS reagent, >=98.5% xylenes + ethylbenzene basis
Xylenes reagent
Xylenes, ACS reagent
Xylenes, reagent grade
Xylenes, histological grade
Xylenes, puriss., 98.0%
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2-Xylene; 1,3-xylene; 1,4-xylene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.9780 97.80%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.6653 66.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9724 97.24%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7199 71.99%
P-glycoprotein inhibitior - 0.9703 97.03%
P-glycoprotein substrate - 0.9747 97.47%
CYP3A4 substrate - 0.7352 73.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.8632 86.32%
CYP2C9 inhibition - 0.7531 75.31%
CYP2C19 inhibition - 0.5515 55.15%
CYP2D6 inhibition - 0.9110 91.10%
CYP1A2 inhibition + 0.5339 53.39%
CYP2C8 inhibition - 0.9058 90.58%
CYP inhibitory promiscuity + 0.7518 75.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Warning 0.3948 39.48%
Eye corrosion - 0.6992 69.92%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7163 71.63%
Skin corrosion - 0.9889 98.89%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5747 57.47%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.8804 88.04%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5151 51.51%
Acute Oral Toxicity (c) III 0.8319 83.19%
Estrogen receptor binding - 0.7944 79.44%
Androgen receptor binding - 0.5066 50.66%
Thyroid receptor binding - 0.8179 81.79%
Glucocorticoid receptor binding - 0.8494 84.94%
Aromatase binding - 0.7440 74.40%
PPAR gamma - 0.8575 85.75%
Honey bee toxicity - 0.9852 98.52%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9919 99.19%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.67% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.94% 94.73%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 88.03% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.99% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.79% 86.33%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 85.75% 83.14%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.23% 93.65%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 83.63% 81.29%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.33% 90.93%
CHEMBL240 Q12809 HERG 81.86% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.77% 91.11%
CHEMBL3961 Q15759 MAP kinase p38 beta 80.57% 94.75%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.14% 100.00%

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.
Panax ginseng

Cross-Links

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PubChem 6850715
NPASS NPC167137