4-Carboxy-3-methyl-phenolate

Details

Top
Internal ID 9a525f9a-32c4-4969-b587-2dae38705fdb
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 4-carboxy-3-methylphenolate
SMILES (Canonical) CC1=C(C=CC(=C1)[O-])C(=O)O
SMILES (Isomeric) CC1=C(C=CC(=C1)[O-])C(=O)O
InChI InChI=1S/C8H8O3/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4,9H,1H3,(H,10,11)/p-1
InChI Key BBMFSGOFUHEVNP-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H7O3-
Molecular Weight 151.14 g/mol
Exact Mass 151.039519081 g/mol
Topological Polar Surface Area (TPSA) 60.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 0.77
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
4-carboxy-3-methyl-phenolate
CHEBI:165213

2D Structure

Top
2D Structure of 4-Carboxy-3-methyl-phenolate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9231 92.31%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.9427 94.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9615 96.15%
OATP1B3 inhibitior + 0.9795 97.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9664 96.64%
P-glycoprotein inhibitior - 0.9820 98.20%
P-glycoprotein substrate - 0.9797 97.97%
CYP3A4 substrate - 0.8183 81.83%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.9154 91.54%
CYP3A4 inhibition - 0.9648 96.48%
CYP2C9 inhibition - 0.9401 94.01%
CYP2C19 inhibition - 0.9500 95.00%
CYP2D6 inhibition - 0.9613 96.13%
CYP1A2 inhibition - 0.9144 91.44%
CYP2C8 inhibition - 0.8003 80.03%
CYP inhibitory promiscuity - 0.9607 96.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6410 64.10%
Carcinogenicity (trinary) Non-required 0.6810 68.10%
Eye corrosion + 0.8267 82.67%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9311 93.11%
Skin corrosion - 0.6879 68.79%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8581 85.81%
Micronuclear + 0.5296 52.96%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.6074 60.74%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6373 63.73%
Acute Oral Toxicity (c) III 0.6880 68.80%
Estrogen receptor binding - 0.8659 86.59%
Androgen receptor binding - 0.6009 60.09%
Thyroid receptor binding - 0.8078 80.78%
Glucocorticoid receptor binding - 0.7951 79.51%
Aromatase binding - 0.8539 85.39%
PPAR gamma - 0.8183 81.83%
Honey bee toxicity - 0.9891 98.91%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.9265 92.65%
Fish aquatic toxicity + 0.9414 94.14%

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 90.73% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.32% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.28% 98.95%
CHEMBL4208 P20618 Proteasome component C5 86.78% 90.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.54% 97.21%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.18% 93.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.95% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.17% 87.67%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.68% 96.95%

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.
Aquilaria sinensis
Cullen corylifolium
Psammosilene tunicoides

Cross-Links

Top
PubChem 54678414
NPASS NPC3128