CID 20375919

Details

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Internal ID 05c32379-a82d-4ae1-a1e1-5af026c7fb44
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name benzaldehyde
SMILES (Canonical) C1=CC=C(C=C1)C=O.C1=CC=C(C=C1)C=O
SMILES (Isomeric) C1=CC=C(C=C1)C=O.C1=CC=C(C=C1)C=O
InChI InChI=1S/2C7H6O/c2*8-6-7-4-2-1-3-5-7/h2*1-6H
InChI Key BHLWLVTYEDJFGZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H12O2
Molecular Weight 212.24 g/mol
Exact Mass 212.083729621 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 0.00
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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A804633

2D Structure

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2D Structure of CID 20375919

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.9661 96.61%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7613 76.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9202 92.02%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.9948 99.48%
CYP3A4 substrate - 0.8575 85.75%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.7276 72.76%
CYP3A4 inhibition - 0.9571 95.71%
CYP2C9 inhibition - 0.8401 84.01%
CYP2C19 inhibition - 0.7575 75.75%
CYP2D6 inhibition - 0.9322 93.22%
CYP1A2 inhibition + 0.5245 52.45%
CYP2C8 inhibition - 0.9443 94.43%
CYP inhibitory promiscuity - 0.6968 69.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5523 55.23%
Carcinogenicity (trinary) Non-required 0.7084 70.84%
Eye corrosion + 0.5898 58.98%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7200 72.00%
Skin corrosion - 0.5724 57.24%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8556 85.56%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.8842 88.42%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5399 53.99%
Acute Oral Toxicity (c) III 0.5323 53.23%
Estrogen receptor binding - 0.8697 86.97%
Androgen receptor binding - 0.7132 71.32%
Thyroid receptor binding - 0.8132 81.32%
Glucocorticoid receptor binding - 0.9401 94.01%
Aromatase binding - 0.7435 74.35%
PPAR gamma - 0.8938 89.38%
Honey bee toxicity - 0.9510 95.10%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9558 95.58%

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 96.69% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.29% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.97% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.57% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.98% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.39% 94.73%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.01% 94.23%

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.
There are no matching plants.

Cross-Links

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PubChem 20375919
NPASS NPC97117