Mesitylene

Details

Top
Internal ID 337c634e-d668-4d27-802e-301d82055753
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1,3,5-trimethylbenzene
SMILES (Canonical) CC1=CC(=CC(=C1)C)C
SMILES (Isomeric) CC1=CC(=CC(=C1)C)C
InChI InChI=1S/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H3
InChI Key AUHZEENZYGFFBQ-UHFFFAOYSA-N
Popularity 3,986 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12
Molecular Weight 120.19 g/mol
Exact Mass 120.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
1,3,5-Trimethylbenzene
108-67-8
sym-Trimethylbenzene
3,5-Dimethyltoluene
Fleet-X
Trimethylbenzol
Benzene, 1,3,5-trimethyl-
s-Trimethylbenzene
2,4,6-trimethylbenzene
NSC 9273
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Mesitylene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.8881 88.81%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9429 94.29%
Subcellular localzation Lysosomes 0.5862 58.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9673 96.73%
OATP1B3 inhibitior + 0.9654 96.54%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9017 90.17%
P-glycoprotein inhibitior - 0.9887 98.87%
P-glycoprotein substrate - 0.9960 99.60%
CYP3A4 substrate - 0.8549 85.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.9269 92.69%
CYP2C9 inhibition - 0.9572 95.72%
CYP2C19 inhibition - 0.9627 96.27%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8304 83.04%
CYP2C8 inhibition - 0.9953 99.53%
CYP inhibitory promiscuity - 0.8017 80.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5164 51.64%
Carcinogenicity (trinary) Warning 0.5628 56.28%
Eye corrosion + 0.9925 99.25%
Eye irritation + 0.9942 99.42%
Skin irritation + 0.9378 93.78%
Skin corrosion - 0.9180 91.80%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7355 73.55%
Micronuclear - 0.9668 96.68%
Hepatotoxicity + 0.9375 93.75%
skin sensitisation + 0.9405 94.05%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.8705 87.05%
Nephrotoxicity + 0.4509 45.09%
Acute Oral Toxicity (c) III 0.7939 79.39%
Estrogen receptor binding - 0.9498 94.98%
Androgen receptor binding - 0.8301 83.01%
Thyroid receptor binding - 0.8339 83.39%
Glucocorticoid receptor binding - 0.8724 87.24%
Aromatase binding - 0.8726 87.26%
PPAR gamma - 0.8913 89.13%
Honey bee toxicity - 0.9696 96.96%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.8928 89.28%

Targets

Top

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
CHEMBL3401 O75469 Pregnane X receptor 83.99% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.23% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.45% 94.80%
CHEMBL2581 P07339 Cathepsin D 80.83% 98.95%

Plants that contains it

Top
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.
Arachis hypogaea
Chaenomeles sinensis
Crocus sativus
Ferulago nodosa
Lepidium meyenii

Cross-Links

Top
PubChem 7947
NPASS NPC64270
LOTUS LTS0113640
wikiData Q425161