3,5-Dimethylbenzaldehyde

Details

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Internal ID 1dcb9577-77bb-4ff1-b194-88d7c32f3658
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name 3,5-dimethylbenzaldehyde
SMILES (Canonical) CC1=CC(=CC(=C1)C=O)C
SMILES (Isomeric) CC1=CC(=CC(=C1)C=O)C
InChI InChI=1S/C9H10O/c1-7-3-8(2)5-9(4-7)6-10/h3-6H,1-2H3
InChI Key NBEFMISJJNGCIZ-UHFFFAOYSA-N
Popularity 34 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O
Molecular Weight 134.17 g/mol
Exact Mass 134.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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5779-95-3
Benzaldehyde, 3,5-dimethyl-
3,5-Dimethyl benzaldehyde
MFCD00082777
m-Xylene-5-carboxaldehyde
3,5-DiMethyl-Benzaldehyde
3,5-dimehtylbenzaldehyde
3,5-Dimethylbenzaldehyde #
SCHEMBL280640
3,5-Dimethylbenzaldehyde, 97%
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,5-Dimethylbenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8944 89.44%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5773 57.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8986 89.86%
OATP1B3 inhibitior + 0.9714 97.14%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9102 91.02%
P-glycoprotein inhibitior - 0.9815 98.15%
P-glycoprotein substrate - 0.9922 99.22%
CYP3A4 substrate - 0.7680 76.80%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7537 75.37%
CYP3A4 inhibition - 0.9610 96.10%
CYP2C9 inhibition - 0.9698 96.98%
CYP2C19 inhibition - 0.9599 95.99%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.7071 70.71%
CYP2C8 inhibition - 0.9890 98.90%
CYP inhibitory promiscuity - 0.8883 88.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5164 51.64%
Carcinogenicity (trinary) Non-required 0.7129 71.29%
Eye corrosion + 0.9962 99.62%
Eye irritation + 0.9858 98.58%
Skin irritation + 0.9403 94.03%
Skin corrosion - 0.7368 73.68%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7104 71.04%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation + 0.9702 97.02%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.6004 60.04%
Acute Oral Toxicity (c) III 0.9399 93.99%
Estrogen receptor binding - 0.9414 94.14%
Androgen receptor binding - 0.8467 84.67%
Thyroid receptor binding - 0.8372 83.72%
Glucocorticoid receptor binding - 0.9068 90.68%
Aromatase binding - 0.8471 84.71%
PPAR gamma - 0.8992 89.92%
Honey bee toxicity - 0.9337 93.37%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8007 80.07%

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 95.52% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.88% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.77% 94.80%
CHEMBL1951 P21397 Monoamine oxidase A 84.54% 91.49%
CHEMBL2581 P07339 Cathepsin D 82.92% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.21% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.04% 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.
Crocus sativus

Cross-Links

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PubChem 34225
NPASS NPC270832