Salicylate

Details

Top
Internal ID 43a0f6f7-911d-409b-ac67-3095c9f8c58f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Salicylic acid and derivatives > Salicylic acids
IUPAC Name 2-carboxyphenolate
SMILES (Canonical) C1=CC=C(C(=C1)C(=O)O)[O-]
SMILES (Isomeric) C1=CC=C(C(=C1)C(=O)O)[O-]
InChI InChI=1S/C7H6O3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H,(H,9,10)/p-1
InChI Key YGSDEFSMJLZEOE-UHFFFAOYSA-M
Popularity 13,398 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H5O3-
Molecular Weight 137.11 g/mol
Exact Mass 137.023869017 g/mol
Topological Polar Surface Area (TPSA) 60.40 Ų
XlogP 2.40
Atomic LogP (AlogP) 0.46
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
2-Hydroxybenzoate
o-Hydroxybenzoate
Salicylate ion
Salicylate anion
2-carboxyphenolate
o-Hydroxybenzoate anion
2-Hydroxybenzoic acid ion(1-)
Salicylic acid, ion(1-)
63-36-5
2-hydroxy-benzoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Salicylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9858 98.58%
Caco-2 + 0.9313 93.13%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.9152 91.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9674 96.74%
OATP1B3 inhibitior + 0.9815 98.15%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9563 95.63%
P-glycoprotein inhibitior - 0.9884 98.84%
P-glycoprotein substrate - 0.9930 99.30%
CYP3A4 substrate - 0.8596 85.96%
CYP2C9 substrate - 0.6146 61.46%
CYP2D6 substrate - 0.8927 89.27%
CYP3A4 inhibition - 0.9707 97.07%
CYP2C9 inhibition - 0.9700 97.00%
CYP2C19 inhibition - 0.8946 89.46%
CYP2D6 inhibition - 0.9567 95.67%
CYP1A2 inhibition - 0.9420 94.20%
CYP2C8 inhibition - 0.9112 91.12%
CYP inhibitory promiscuity - 0.9616 96.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6499 64.99%
Carcinogenicity (trinary) Non-required 0.6828 68.28%
Eye corrosion + 0.7174 71.74%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9554 95.54%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9131 91.31%
Micronuclear + 0.6396 63.96%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.7033 70.33%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5514 55.14%
Acute Oral Toxicity (c) III 0.8183 81.83%
Estrogen receptor binding - 0.9228 92.28%
Androgen receptor binding - 0.8127 81.27%
Thyroid receptor binding - 0.6858 68.58%
Glucocorticoid receptor binding - 0.8989 89.89%
Aromatase binding - 0.8889 88.89%
PPAR gamma - 0.5402 54.02%
Honey bee toxicity - 0.9777 97.77%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.9277 92.77%

Targets

Top

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 91.44% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.73% 94.62%
CHEMBL2581 P07339 Cathepsin D 82.67% 98.95%
CHEMBL5847 P52895 Aldo-keto reductase family 1 member C2 82.47% 92.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.90% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.28% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.95% 87.67%

Plants that contains it

Top
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.
Abrus melanospermus subsp. melanospermus
Artemisia capillaris
Cephalotaxus fortunei
Diospyros kaki
Fagopyrum esculentum
Glehnia littoralis
Isatis tinctoria
Laggera alata
Rubus idaeus
Senna alexandrina

Cross-Links

Top
PubChem 54675850
NPASS NPC20045