p-Hydroxymercuribenzoic acid

Identification

Name
p-Hydroxymercuribenzoic acid
Accession Number
DB01671
Description
Not Available
Type
Small Molecule
Groups
Experimental
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Structure
Thumb
Weight
Average: 338.71
Monoisotopic: 340.002319662
Chemical Formula
C7H6HgO3
Synonyms
  • (p-carboxyphenyl)hydroxymercury

Pharmacology

Indication
Not Available
Contraindications & Blackbox Warnings
Learn about our commercial Contraindications & Blackbox Warnings data.
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Pharmacodynamics
Not Available
Mechanism of action
TargetActionsOrganism
UCarbonic anhydrase 2Not AvailableHumans
Absorption
Not Available
Volume of distribution
Not Available
Protein binding
Not Available
Metabolism
Not Available
Route of elimination
Not Available
Half-life
Not Available
Clearance
Not Available
Adverse Effects
Learn about our commercial Adverse Effects data.
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Toxicity
Not Available
Affected organisms
Not Available
Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Categories

Drug Categories
Chemical TaxonomyProvided by Classyfire
Description
This compound belongs to the class of organic compounds known as 4-mercuribenzoic acids. These are benzoic acids containing a mercury atom attached to the 4-position of the benzene moiety.
Kingdom
Organic compounds
Super Class
Benzenoids
Class
Benzene and substituted derivatives
Sub Class
Benzoic acids and derivatives
Direct Parent
4-Mercuribenzoic acids
Alternative Parents
Benzoyl derivatives / Metal aryls / Aryl mercury compounds / Organic transition metal salts / Monocarboxylic acids and derivatives / Carboxylic acids / Organooxygen compounds / Organic oxoanionic compounds / Organic oxides / Hydrocarbon derivatives
Substituents
4-mercuribenzoic acid / Aromatic homomonocyclic compound / Aryl mercury compound / Benzoyl / Carboxylic acid / Carboxylic acid derivative / Hydrocarbon derivative / Metal aryl / Monocarboxylic acid or derivatives / Organic hydroxide
Molecular Framework
Aromatic homomonocyclic compounds
External Descriptors
mercuribenzoic acid (CHEBI:49644)

Chemical Identifiers

UNII
848QN6RR3O
CAS number
1126-48-3
InChI Key
WMHRYLDWLOGHSG-UHFFFAOYSA-M
InChI
InChI=1S/C7H5O2.Hg.H2O/c8-7(9)6-4-2-1-3-5-6;;/h2-5H,(H,8,9);;1H2/q;+1;/p-1
IUPAC Name
(4-carboxyphenyl)mercurol
SMILES
O[Hg]C1=CC=C(C=C1)C(O)=O

References

General References
Not Available
PubChem Compound
14309
PubChem Substance
46506059
ChemSpider
8264069
BindingDB
50351172
ChEBI
49644
PDBe Ligand
HGB
PDB Entries
1bv3 / 1f2w / 1ze8 / 2aw1 / 2f14 / 3ibi / 3ibl / 3ibn / 3ibu / 3k34
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Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Solid
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility52.2 mg/mLALOGPS
logP0.43ALOGPS
logP-0.12ChemAxon
logS-0.81ALOGPS
pKa (Strongest Acidic)3.86ChemAxon
pKa (Strongest Basic)-2.4ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area57.53 Å2ChemAxon
Rotatable Bond Count2ChemAxon
Refractivity35.3 m3·mol-1ChemAxon
Polarizability15.68 Å3ChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted ADMET Features
PropertyValueProbability
Human Intestinal Absorption+0.9512
Blood Brain Barrier+0.8998
Caco-2 permeable+0.6906
P-glycoprotein substrateNon-substrate0.8205
P-glycoprotein inhibitor INon-inhibitor0.9889
P-glycoprotein inhibitor IINon-inhibitor1.0
Renal organic cation transporterNon-inhibitor0.9332
CYP450 2C9 substrateNon-substrate0.8373
CYP450 2D6 substrateNon-substrate0.9328
CYP450 3A4 substrateNon-substrate0.8125
CYP450 1A2 substrateNon-inhibitor0.8095
CYP450 2C9 inhibitorNon-inhibitor0.8935
CYP450 2D6 inhibitorNon-inhibitor0.8988
CYP450 2C19 inhibitorNon-inhibitor0.9405
CYP450 3A4 inhibitorNon-inhibitor0.9484
CYP450 inhibitory promiscuityLow CYP Inhibitory Promiscuity0.9732
Ames testNon AMES toxic0.887
CarcinogenicityNon-carcinogens0.5473
BiodegradationReady biodegradable0.57
Rat acute toxicity1.6700 LD50, mol/kg Not applicable
hERG inhibition (predictor I)Weak inhibitor0.9708
hERG inhibition (predictor II)Non-inhibitor0.9768
ADMET data is predicted using admetSAR, a free tool for evaluating chemical ADMET properties. (23092397)

Spectra

Mass Spec (NIST)
Not Available
Spectra
Not Available

Targets

Kind
Protein
Organism
Humans
Pharmacological action
Unknown
General Function
Zinc ion binding
Specific Function
Essential for bone resorption and osteoclast differentiation (By similarity). Reversible hydration of carbon dioxide. Can hydrate cyanamide to urea. Involved in the regulation of fluid secretion in...
Gene Name
CA2
Uniprot ID
P00918
Uniprot Name
Carbonic anhydrase 2
Molecular Weight
29245.895 Da
References
  1. Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. [PubMed:17139284]
  2. Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. [PubMed:17016423]

Drug created on June 13, 2005 07:24 / Updated on June 12, 2020 10:51

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