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Details

Stereochemistry RACEMIC
Molecular Formula C5H11HgN2O2.Cl
Molecular Weight 367.2
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORMERODRIN

SMILES

[Cl-].COC(C[Hg+])CNC(N)=O

InChI

InChIKey=BJFGVYCULWBXKF-UHFFFAOYSA-M
InChI=1S/C5H11N2O2.ClH.Hg/c1-4(9-2)3-7-5(6)8;;/h4H,1,3H2,2H3,(H3,6,7,8);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 C5H11HgN2O2
Molecular Weight 331.74
Charge 1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

CHLORMERODRIN, an isourea derivative, is an organomercury compound that was previously used as a diuretic. Its radiolabelled (197Hg, 203Hg) forms were used as diagnostics in renal imaging and brain scans.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Neohydrin

Approved Use

Diuretic, for the treatment of edema and congestive heart failure

Launch Date

-5.6808001E11
PubMed

PubMed

TitleDatePubMed
Chlormerodrin: clinical effectiveness and absence of toxicity in congestive heart failure; report of a four-year study.
1959 Apr 4
EFFECTS OF CHLORMERODRIN, P-CHLOROMERCURIBENZOATE AND DICHLORPHENAMIDE ON RENAL SODIUM REABSORPTION AND OXYGEN CONSUMPTION.
1964
COMPARATIVE STUDIES ON MERCURATED 1-, 3-, AND 5- ALLYLHYDANTOINS AND CHLORMERODRIN.
1964 Jun 1
Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:16 UTC 2023
Edited
by admin
on Fri Dec 15 14:59:16 UTC 2023
Record UNII
99T5TWO621
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORMERODRIN
INN   MI   WHO-DD  
INN  
Official Name English
Chlormerodrin [WHO-DD]
Common Name English
CHLORMERODRIN [MI]
Common Name English
(3-(CHLOROMERCURI)-2-METHOXYPROPYL))UREA
Common Name English
NSC-19911
Code English
NEOHYDRIN
Brand Name English
MERCLORAN
Brand Name English
chlormerodrin [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C448
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
Code System Code Type Description
WIKIPEDIA
Chlormerodrin
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
DRUG BANK
DB00534
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
FDA UNII
99T5TWO621
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
MERCK INDEX
m3375
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY Merck Index
PUBCHEM
2716
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110562
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
NCI_THESAURUS
C65315
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-530-4
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
INN
446
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
DRUG CENTRAL
4911
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
CHEBI
59445
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
CAS
62-37-3
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
EVMPD
SUB06184MIG
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
MESH
D002717
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
SMS_ID
100000081563
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
NSC
19911
Created by admin on Fri Dec 15 14:59:16 UTC 2023 , Edited by admin on Fri Dec 15 14:59:16 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY