Salicylamide

Details

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Internal ID 2b66ba2b-9ee4-4206-a436-98d61bbf841d
Taxonomy Benzenoids > Phenols > 1-hydroxy-4-unsubstituted benzenoids
IUPAC Name 2-hydroxybenzamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)
InChI Key SKZKKFZAGNVIMN-UHFFFAOYSA-N
Popularity 2,544 references in papers

Physical and Chemical Properties

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Molecular Formula C7H7NO2
Molecular Weight 137.14 g/mol
Exact Mass 137.047678466 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.49
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2-Hydroxybenzamide
65-45-2
o-Hydroxybenzamide
2-Carbamoylphenol
Salicylic acid amide
Benzamide, 2-hydroxy-
Salamide
Urtosal
2-Carboxamidophenol
Algiamida
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Salicylamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9234 92.34%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9816 98.16%
OATP1B3 inhibitior + 0.9597 95.97%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9593 95.93%
P-glycoprotein inhibitior - 0.9903 99.03%
P-glycoprotein substrate - 0.9847 98.47%
CYP3A4 substrate - 0.7955 79.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8693 86.93%
CYP3A4 inhibition - 0.8828 88.28%
CYP2C9 inhibition - 0.9520 95.20%
CYP2C19 inhibition - 0.8779 87.79%
CYP2D6 inhibition - 0.9043 90.43%
CYP1A2 inhibition - 0.7061 70.61%
CYP2C8 inhibition - 0.9383 93.83%
CYP inhibitory promiscuity - 0.9144 91.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7022 70.22%
Carcinogenicity (trinary) Non-required 0.6714 67.14%
Eye corrosion - 0.9886 98.86%
Eye irritation + 0.9974 99.74%
Skin irritation - 0.7388 73.88%
Skin corrosion - 0.9849 98.49%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9094 90.94%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.6427 64.27%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6070 60.70%
Acute Oral Toxicity (c) III 0.8030 80.30%
Estrogen receptor binding - 0.9192 91.92%
Androgen receptor binding - 0.7565 75.65%
Thyroid receptor binding - 0.6174 61.74%
Glucocorticoid receptor binding - 0.8803 88.03%
Aromatase binding - 0.8515 85.15%
PPAR gamma - 0.7773 77.73%
Honey bee toxicity - 0.9748 97.48%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.7595 75.95%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.51% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.70% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.55% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.48% 95.50%

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 5147
LOTUS LTS0156083
wikiData Q2496906