1,2,3,5-Tetramethylbenzene

Details

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Internal ID eeff19de-e118-4c5e-87dc-0348d30bff42
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1,2,3,5-tetramethylbenzene
SMILES (Canonical) CC1=CC(=C(C(=C1)C)C)C
SMILES (Isomeric) CC1=CC(=C(C(=C1)C)C)C
InChI InChI=1S/C10H14/c1-7-5-8(2)10(4)9(3)6-7/h5-6H,1-4H3
InChI Key BFIMMTCNYPIMRN-UHFFFAOYSA-N
Popularity 240 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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527-53-7
Isodurene
Benzene, 1,2,3,5-tetramethyl-
1,3,4,5-Tetramethylbenzene
NSC 8091
EINECS 208-417-1
UNII-0JBI5Y5A5Z
0JBI5Y5A5Z
1,2,3,5-tetramethyl-benzene
CCRIS 8661
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2,3,5-Tetramethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.8629 86.29%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.9429 94.29%
Subcellular localzation Mitochondria 0.5629 56.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9634 96.34%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8580 85.80%
P-glycoprotein inhibitior - 0.9805 98.05%
P-glycoprotein substrate - 0.9768 97.68%
CYP3A4 substrate - 0.8143 81.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7340 73.40%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.9261 92.61%
CYP2C19 inhibition - 0.8939 89.39%
CYP2D6 inhibition - 0.9356 93.56%
CYP1A2 inhibition - 0.6775 67.75%
CYP2C8 inhibition - 0.9878 98.78%
CYP inhibitory promiscuity - 0.6329 63.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Warning 0.5220 52.20%
Eye corrosion + 0.9721 97.21%
Eye irritation + 0.9873 98.73%
Skin irritation + 0.9313 93.13%
Skin corrosion - 0.9713 97.13%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6186 61.86%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.8660 86.60%
skin sensitisation + 0.9512 95.12%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5896 58.96%
Acute Oral Toxicity (c) III 0.6305 63.05%
Estrogen receptor binding - 0.9336 93.36%
Androgen receptor binding - 0.7899 78.99%
Thyroid receptor binding - 0.7646 76.46%
Glucocorticoid receptor binding - 0.8658 86.58%
Aromatase binding - 0.8184 81.84%
PPAR gamma - 0.9086 90.86%
Honey bee toxicity - 0.9751 97.51%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity + 0.9604 96.04%

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
CHEMBL3401 O75469 Pregnane X receptor 85.73% 94.73%
CHEMBL2581 P07339 Cathepsin D 82.50% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.49% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.42% 94.80%
CHEMBL3568 P29475 Nitric-oxide synthase, brain 81.66% 95.46%

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
Crocus sativus
Curcuma longa
Lycium barbarum
Lycium chinense

Cross-Links

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PubChem 10695
NPASS NPC113837