2,4,6-Trimethylbenzaldehyde

Details

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Internal ID 696db3d2-3640-42f1-87d9-fe9fe0065f9a
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 2,4,6-trimethylbenzaldehyde
SMILES (Canonical) CC1=CC(=C(C(=C1)C)C=O)C
SMILES (Isomeric) CC1=CC(=C(C(=C1)C)C=O)C
InChI InChI=1S/C10H12O/c1-7-4-8(2)10(6-11)9(3)5-7/h4-6H,1-3H3
InChI Key HIKRJHFHGKZKRI-UHFFFAOYSA-N
Popularity 137 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Mesitaldehyde
487-68-3
Mesitylaldehyde
Benzaldehyde, 2,4,6-trimethyl-
Mesitylenecarboxaldehyde
2-Mesitylenecarboxaldehyde
2-Formylmesitylene
2,4,6-trimethyl-benzaldehyde
EINECS 207-662-1
MFCD00003341
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,6-Trimethylbenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9122 91.22%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.7428 74.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9012 90.12%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9073 90.73%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9888 98.88%
CYP3A4 substrate - 0.7691 76.91%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8082 80.82%
CYP3A4 inhibition - 0.9459 94.59%
CYP2C9 inhibition - 0.9439 94.39%
CYP2C19 inhibition - 0.9048 90.48%
CYP2D6 inhibition - 0.9421 94.21%
CYP1A2 inhibition - 0.5317 53.17%
CYP2C8 inhibition - 0.9810 98.10%
CYP inhibitory promiscuity - 0.7249 72.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6187 61.87%
Eye corrosion + 0.9651 96.51%
Eye irritation + 0.9955 99.55%
Skin irritation + 0.9103 91.03%
Skin corrosion - 0.8359 83.59%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7365 73.65%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.9646 96.46%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5326 53.26%
Acute Oral Toxicity (c) III 0.8847 88.47%
Estrogen receptor binding - 0.9090 90.90%
Androgen receptor binding - 0.7817 78.17%
Thyroid receptor binding - 0.7465 74.65%
Glucocorticoid receptor binding - 0.8903 89.03%
Aromatase binding - 0.8309 83.09%
PPAR gamma - 0.9064 90.64%
Honey bee toxicity - 0.9381 93.81%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9250 92.50%

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 96.36% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 92.09% 98.11%
CHEMBL3401 O75469 Pregnane X receptor 91.55% 94.73%
CHEMBL2581 P07339 Cathepsin D 86.97% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.64% 94.80%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 80.90% 95.70%
CHEMBL3568 P29475 Nitric-oxide synthase, brain 80.35% 95.46%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.13% 96.00%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 10254
NPASS NPC164526