2-Formyl-6-hydroxybenzoic acid

Details

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Internal ID 638a2be0-28f4-455a-8161-9e31bfd4f4a7
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Salicylic acid and derivatives > Salicylic acids
IUPAC Name 2-formyl-6-hydroxybenzoic acid
SMILES (Canonical) C1=CC(=C(C(=C1)O)C(=O)O)C=O
SMILES (Isomeric) C1=CC(=C(C(=C1)O)C(=O)O)C=O
InChI InChI=1S/C8H6O4/c9-4-5-2-1-3-6(10)7(5)8(11)12/h1-4,10H,(H,11,12)
InChI Key HBZPATAKQIDUTN-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O4
Molecular Weight 166.13 g/mol
Exact Mass 166.02660867 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 0.90
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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6-formylsalicylic acid
4743-48-0
SCHEMBL20975456
MB25604

2D Structure

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2D Structure of 2-Formyl-6-hydroxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9200 92.00%
Caco-2 + 0.8934 89.34%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8536 85.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9361 93.61%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior + 0.6800 68.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9726 97.26%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9695 96.95%
CYP3A4 substrate - 0.7255 72.55%
CYP2C9 substrate - 0.6931 69.31%
CYP2D6 substrate - 0.8936 89.36%
CYP3A4 inhibition - 0.8608 86.08%
CYP2C9 inhibition - 0.7515 75.15%
CYP2C19 inhibition - 0.9107 91.07%
CYP2D6 inhibition - 0.9504 95.04%
CYP1A2 inhibition - 0.9753 97.53%
CYP2C8 inhibition - 0.9389 93.89%
CYP inhibitory promiscuity - 0.9463 94.63%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7346 73.46%
Carcinogenicity (trinary) Non-required 0.8203 82.03%
Eye corrosion - 0.8586 85.86%
Eye irritation + 0.9971 99.71%
Skin irritation + 0.8330 83.30%
Skin corrosion - 0.9074 90.74%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9093 90.93%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.6696 66.96%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5496 54.96%
Acute Oral Toxicity (c) III 0.5586 55.86%
Estrogen receptor binding - 0.8447 84.47%
Androgen receptor binding - 0.7994 79.94%
Thyroid receptor binding - 0.6451 64.51%
Glucocorticoid receptor binding - 0.8382 83.82%
Aromatase binding - 0.8574 85.74%
PPAR gamma - 0.5239 52.39%
Honey bee toxicity - 0.9805 98.05%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.9547 95.47%

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 97.02% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.97% 98.11%
CHEMBL3194 P02766 Transthyretin 90.30% 90.71%
CHEMBL2581 P07339 Cathepsin D 88.44% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.59% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.70% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.55% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 54441948
LOTUS LTS0115197
wikiData Q77489760