2,4,5-Trimethylbenzaldehyde

Details

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Internal ID 83e429f7-6440-4c3d-93cf-0b9a9eca6750
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 2,4,5-trimethylbenzaldehyde
SMILES (Canonical) CC1=CC(=C(C=C1C)C=O)C
SMILES (Isomeric) CC1=CC(=C(C=C1C)C=O)C
InChI InChI=1S/C10H12O/c1-7-4-9(3)10(6-11)5-8(7)2/h4-6H,1-3H3
InChI Key LROJZZICACKNJL-UHFFFAOYSA-N
Popularity 15 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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5779-72-6
Duryl aldehyde
Duraldehyde
Durylaldehyde
Benzaldehyde, 2,4,5-trimethyl-
MFCD00017713
2,4,5-TriMethyl-Benzaldehyde
SCHEMBL97117
LROJZZICACKNJL-UHFFFAOYSA-
DTXSID80206482
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,5-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 + 0.9100 91.00%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7428 74.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8584 85.84%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8426 84.26%
P-glycoprotein inhibitior - 0.9746 97.46%
P-glycoprotein substrate - 0.9829 98.29%
CYP3A4 substrate - 0.7440 74.40%
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 - 0.9766 97.66%
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 + 0.9918 99.18%
Skin irritation + 0.9103 91.03%
Skin corrosion - 0.8359 83.59%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6558 65.58%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.9646 96.46%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5342 53.42%
Acute Oral Toxicity (c) III 0.8847 88.47%
Estrogen receptor binding - 0.8946 89.46%
Androgen receptor binding - 0.8627 86.27%
Thyroid receptor binding - 0.7453 74.53%
Glucocorticoid receptor binding - 0.8819 88.19%
Aromatase binding - 0.7406 74.06%
PPAR gamma - 0.8673 86.73%
Honey bee toxicity - 0.9594 95.94%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.20% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.11% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.88% 94.73%
CHEMBL4208 P20618 Proteasome component C5 83.44% 90.00%
CHEMBL2581 P07339 Cathepsin D 83.07% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.14% 86.33%

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
Crocus sativus
Lonicera japonica

Cross-Links

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PubChem 22013
NPASS NPC93135