Tiron free acid

Details

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Internal ID 5ec06f81-65ef-4e5d-b82e-d516c677aa8f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzenesulfonic acids and derivatives
IUPAC Name 4,5-dihydroxybenzene-1,3-disulfonic acid
SMILES (Canonical) C1=C(C=C(C(=C1O)O)S(=O)(=O)O)S(=O)(=O)O
SMILES (Isomeric) C1=C(C=C(C(=C1O)O)S(=O)(=O)O)S(=O)(=O)O
InChI InChI=1S/C6H6O8S2/c7-4-1-3(15(9,10)11)2-5(6(4)8)16(12,13)14/h1-2,7-8H,(H,9,10,11)(H,12,13,14)
InChI Key XXAXVMUWHZHZMJ-UHFFFAOYSA-N
Popularity 1,334 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O8S2
Molecular Weight 270.20 g/mol
Exact Mass 269.95040949 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.41
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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149-46-2
CHYMOPAPAIN
4,5-dihydroxybenzene-1,3-disulfonic acid
1,3-Benzenedisulfonic acid, 4,5-dihydroxy-
3,5-Disulfopyrocatechol
4,5-Dihydroxy-1,3-benzenedisulfonic acid
Pyrocatechol-3,5-disulfonic acid
Tiferron
m-Benzenedisulfonic acid, 4,5-dihydroxy-
Sodium catechol sulfate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tiron free acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6052 60.52%
Caco-2 - 0.8636 86.36%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4981 49.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9849 98.49%
P-glycoprotein inhibitior - 0.9618 96.18%
P-glycoprotein substrate - 0.9709 97.09%
CYP3A4 substrate - 0.7192 71.92%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8258 82.58%
CYP3A4 inhibition - 0.9830 98.30%
CYP2C9 inhibition - 0.7836 78.36%
CYP2C19 inhibition - 0.7645 76.45%
CYP2D6 inhibition - 0.9187 91.87%
CYP1A2 inhibition - 0.7428 74.28%
CYP2C8 inhibition - 0.9667 96.67%
CYP inhibitory promiscuity - 0.9191 91.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.7963 79.63%
Carcinogenicity (trinary) Non-required 0.6704 67.04%
Eye corrosion - 0.9245 92.45%
Eye irritation + 0.6635 66.35%
Skin irritation - 0.7239 72.39%
Skin corrosion + 0.8850 88.50%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8415 84.15%
Micronuclear + 0.9400 94.00%
Hepatotoxicity + 0.6680 66.80%
skin sensitisation - 0.7688 76.88%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8151 81.51%
Acute Oral Toxicity (c) III 0.7956 79.56%
Estrogen receptor binding - 0.8709 87.09%
Androgen receptor binding - 0.8439 84.39%
Thyroid receptor binding - 0.7990 79.90%
Glucocorticoid receptor binding - 0.7801 78.01%
Aromatase binding - 0.8431 84.31%
PPAR gamma - 0.8546 85.46%
Honey bee toxicity - 0.8881 88.81%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9812 98.12%

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 94.43% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.66% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.14% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.74% 92.94%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.26% 94.42%
CHEMBL3401 O75469 Pregnane X receptor 83.05% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.85% 94.00%

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.
Carica papaya

Cross-Links

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PubChem 9002
LOTUS LTS0010034
wikiData Q27255921