2,3,4-Trimethylbenzaldehyde

Details

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Internal ID 43424de5-192d-4f99-add6-b832fefa47c0
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 2,3,4-trimethylbenzaldehyde
SMILES (Canonical) CC1=C(C(=C(C=C1)C=O)C)C
SMILES (Isomeric) CC1=C(C(=C(C=C1)C=O)C)C
InChI InChI=1S/C10H12O/c1-7-4-5-10(6-11)9(3)8(7)2/h4-6H,1-3H3
InChI Key RPZOPDOUASNMNP-UHFFFAOYSA-N
Popularity 21 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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34341-28-1
70679-68-4
SCHEMBL366594
DTXSID30372909
AKOS004907327
BENZALDEHYDE, 2,3,4-TRIMETHYL-
EN300-746797
Z1216815451

2D Structure

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2D Structure of 2,3,4-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 + 0.9346 93.46%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7428 74.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8643 86.43%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8950 89.50%
P-glycoprotein inhibitior - 0.9839 98.39%
P-glycoprotein substrate - 0.9774 97.74%
CYP3A4 substrate - 0.7249 72.49%
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 - 0.9169 91.69%
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 + 0.9884 98.84%
Skin irritation + 0.9103 91.03%
Skin corrosion - 0.8359 83.59%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6471 64.71%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.9646 96.46%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6544 65.44%
Acute Oral Toxicity (c) III 0.8847 88.47%
Estrogen receptor binding - 0.9339 93.39%
Androgen receptor binding - 0.8842 88.42%
Thyroid receptor binding - 0.7451 74.51%
Glucocorticoid receptor binding - 0.8867 88.67%
Aromatase binding - 0.8385 83.85%
PPAR gamma - 0.9061 90.61%
Honey bee toxicity - 0.9725 97.25%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5200 52.00%
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 95.29% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.54% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.16% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 86.43% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.00% 98.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.99% 97.36%
CHEMBL1951 P21397 Monoamine oxidase A 81.04% 91.49%

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.
Carum carvi
Hyoscyamus niger
Molopospermum peloponnesiacum
Rubia yunnanensis

Cross-Links

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PubChem 2752597
NPASS NPC92146
LOTUS LTS0049870
wikiData Q82160879