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Details

Stereochemistry ACHIRAL
Molecular Formula C7H5HgO2.Cl
Molecular Weight 357.16
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CHLOROMERCURIBENZOIC ACID

SMILES

[Cl-].OC(=O)C1=CC=C([Hg+])C=C1

InChI

InChIKey=YFZOUMNUDGGHIW-UHFFFAOYSA-M
InChI=1S/C7H5O2.ClH.Hg/c8-7(9)6-4-2-1-3-5-6;;/h2-5H,(H,8,9);1H;/q;;+1/p-1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H4HgO2
Molecular Weight 320.7
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Thiol-reactive metal compounds inhibit NF-kappa B activation by blocking I kappa B kinase.
2000 Jun 1
Acetaldehyde stimulates the activation of latent transforming growth factor-beta1 and induces expression of the type II receptor of the cytokine in rat cultured hepatic stellate cells.
2002 Dec 15
Beneficial effect of oleoylated lipids on paraoxonase 1: protection against oxidative inactivation and stabilization.
2003 Oct 15
3alpha/beta,20beta-hydroxysteroid dehydrogenase (porcine testicular carbonyl reductase) also has a cysteine residue that is involved in binding of cofactor NADPH.
2004 Apr
Modulation of activity and inhibitor sensitivity of rabbit aldose reductase-like protein (AKR1B19) by oxidized glutathione and SH-reagents.
2013 Feb 25
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:17:26 GMT 2023
Edited
by admin
on Sat Dec 16 02:17:26 GMT 2023
Record UNII
E1LE0WZ4BO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-CHLOROMERCURIBENZOIC ACID
Common Name English
NSC-32866
Code English
4-CHLOROMERCURIBENZOIC ACID
Common Name English
Code System Code Type Description
WIKIPEDIA
p-Chloromercuribenzoic acid
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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EPA CompTox
DTXSID8040725
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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PUBCHEM
1730
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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ECHA (EC/EINECS)
200-442-6
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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FDA UNII
E1LE0WZ4BO
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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NSC
32866
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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CHEBI
28420
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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CAS
59-85-8
Created by admin on Sat Dec 16 02:17:26 GMT 2023 , Edited by admin on Sat Dec 16 02:17:26 GMT 2023
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