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Details

Stereochemistry ACHIRAL
Molecular Formula C21H14O6S2.2C6H5Hg
Molecular Weight 981.85
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDRARGAPHEN

SMILES

[Hg+]C1=CC=CC=C1.[Hg+]C2=CC=CC=C2.[O-]S(=O)(=O)C3=CC4=C(C=CC=C4)C=C3CC5=C(C=C6C=CC=CC6=C5)S([O-])(=O)=O

InChI

InChIKey=KDNVJBRRDKAHDA-UHFFFAOYSA-L
InChI=1S/C21H16O6S2.2C6H5.2Hg/c22-28(23,24)20-12-16-7-3-1-5-14(16)9-18(20)11-19-10-15-6-2-4-8-17(15)13-21(19)29(25,26)27;2*1-2-4-6-5-3-1;;/h1-10,12-13H,11H2,(H,22,23,24)(H,25,26,27);2*1-5H;;/q;;;2*+1/p-2

HIDE SMILES / InChI

Molecular Formula C6H5Hg
Molecular Weight 277.69
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C21H14O6S2
Molecular Weight 426.462
Charge -2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Hydrargaphen (also known as penotrane) was studied in trials for patients with herpes genitalia. In the treatment of Trichomonas vaginalis infections, penotrane was the suitable treatment for those patients who have not responded to other treatments. Information about the current use of this drug is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of nystatin ('Nystan') and hydrargaphen ('Penotrane') in the treatment of vaginal candidosis in pregnancy.
1973
HERPES GENITALIS. SURVEY OF THIRTY CASES AND EFFECT OF TREATMENT WITH "PENOTRANE" JELLY.
1963-09
The effect of penotrane on the growth in vitro of Candida albicans and Aspergillus fumigatus.
1952-10
Trichomonas vaginalis infections treated with "penotrane".
1951-08-25

Sample Use Guides

The patient was instructed to apply the jelly liberally twice a day to the lesions and to return after 3 days and after 7 days of treatment.
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:47:31 GMT 2025
Edited
by admin
on Mon Mar 31 18:47:31 GMT 2025
Record UNII
DL2D409P9O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(.MU.-((3,3'-METHYLENEBIS(2-NAPHTHALENESULFONATO-.KAPPA.O))(2-)))DIPHENYLDIMERCURY
Preferred Name English
HYDRARGAPHEN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
PHENYLMERCURIC 3,3'-METHYLENEBIS(2-NAPHTHALENESULPHONATE)
Common Name English
PHENYLMERCURIC 3,3'-METHYLENEBIS(2-NAPHTHALENESULFONATE)
Common Name English
.MU.-(2,2'-BINAPHTHALENE-3-SULFONYLOXY)BIS(PHENYLMERCURY)
Common Name English
HYDRARGAPHEN [MI]
Common Name English
hydrargaphen [INN]
Common Name English
HYDRARGAPHEN [MART.]
Common Name English
Hydrargaphen [WHO-DD]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID901016603
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY
ECHA (EC/EINECS)
238-107-1
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY
FDA UNII
DL2D409P9O
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
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PUBCHEM
10350985
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
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MESH
C005041
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
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MERCK INDEX
m239
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY Merck Index
CAS
14235-86-0
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
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SMS_ID
100000084213
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
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ALANWOOD
hydrargaphen
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY
INN
945
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY
NCI_THESAURUS
C170045
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY
EVMPD
SUB08060MIG
Created by admin on Mon Mar 31 18:47:31 GMT 2025 , Edited by admin on Mon Mar 31 18:47:31 GMT 2025
PRIMARY