4-Hydroxy-3-methoxy-5-sulfobenzoic acid

Details

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Internal ID 77b2740c-5ccd-4563-b95c-423b7c22257c
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzenesulfonic acids and derivatives > Sulfobenzoic acids > 3-sulfobenzoic acids
IUPAC Name 4-hydroxy-3-methoxy-5-sulfobenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8O7S/c1-15-5-2-4(8(10)11)3-6(7(5)9)16(12,13)14/h2-3,9H,1H3,(H,10,11)(H,12,13,14)
InChI Key CHJARSOVVOWISM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O7S
Molecular Weight 248.21 g/mol
Exact Mass 247.99907376 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3-methoxy-5-sulfobenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7651 76.51%
Caco-2 - 0.7496 74.96%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5468 54.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9737 97.37%
P-glycoprotein inhibitior - 0.9444 94.44%
P-glycoprotein substrate - 0.9205 92.05%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8752 87.52%
CYP3A4 inhibition - 0.9836 98.36%
CYP2C9 inhibition - 0.7312 73.12%
CYP2C19 inhibition - 0.7489 74.89%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.6710 67.10%
CYP2C8 inhibition - 0.7163 71.63%
CYP inhibitory promiscuity - 0.9412 94.12%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) + 0.7983 79.83%
Carcinogenicity (trinary) Non-required 0.6676 66.76%
Eye corrosion - 0.8778 87.78%
Eye irritation + 0.9826 98.26%
Skin irritation - 0.7961 79.61%
Skin corrosion + 0.6377 63.77%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8068 80.68%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.6555 65.55%
skin sensitisation - 0.8478 84.78%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6824 68.24%
Acute Oral Toxicity (c) III 0.7683 76.83%
Estrogen receptor binding - 0.5914 59.14%
Androgen receptor binding - 0.9042 90.42%
Thyroid receptor binding - 0.7869 78.69%
Glucocorticoid receptor binding - 0.7201 72.01%
Aromatase binding - 0.8552 85.52%
PPAR gamma - 0.8940 89.40%
Honey bee toxicity - 0.9216 92.16%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9840 98.40%

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 92.96% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 91.04% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.74% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.46% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.75% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.82% 98.95%
CHEMBL3194 P02766 Transthyretin 84.35% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 83.41% 91.19%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.24% 96.09%
CHEMBL2535 P11166 Glucose transporter 81.79% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 81.64% 90.20%

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.
Harpephyllum caffrum

Cross-Links

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PubChem 162817584
LOTUS LTS0265502
wikiData Q104958858