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Details

Stereochemistry RACEMIC
Molecular Formula C10H11N4O5S.Na.3H2O
Molecular Weight 376.319
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CARBAZOCHROME SODIUM SULFONATE HYDRATE

SMILES

O.O.O.[Na+].CN1C(CC2=C\C(=N\NC(N)=O)C(=O)C=C12)S([O-])(=O)=O

InChI

InChIKey=CQGHBSBJJFZEHQ-LWUOGSMXSA-M
InChI=1S/C10H12N4O5S.Na.3H2O/c1-14-7-4-8(15)6(12-13-10(11)16)2-5(7)3-9(14)20(17,18)19;;;;/h2,4,9H,3H2,1H3,(H3,11,13,16)(H,17,18,19);;3*1H2/q;+1;;;/p-1/b12-6-;;;;

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C10H12N4O5S
Molecular Weight 300.291
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 1
Optical Activity ( + / - )

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/13257997

Adrenochrome is one of the principal oxidation products of epinephrine and has no significant pressor action. It has been studied in Europe since 1937 and in America since 1951 for its action in control of bleeding from capillaries and venules. Its role seems independent of the chemistry of coagulation, the vitamin K-prothrombin mechanism, and the function of heparin or the usual anticoagulants. It is alleged to reduce capillary permeability and to increase capillary resistance. Both natural and synthetic adrenochrome are markedly unstable and insoluble. Evolution of the adrenochrome monosemicarbazone sodium salicylate complex has overcome these chemical difficulties. This product is synthetically prepared in America under the trade name Adrenosem and the generic name of carbazochrome. The loss of blood was measured in fifty-three patients who underwent multiple extractions and alveoloplasty under general anesthesia. No local anesthetic was employed in any case. Of the fifty-three patients, twenty-six were prepared preoperatively by the intramuscular injection of 5 mg of carbazochrome (Adrenosem) salicylate one and one-half to two hours prior to the operation. The remaining twenty-seven patients served as a control group. When operations of equal extent and severity were compared, it was found that no effective benefit in reduction of loss of blood at operation was noted in the patients treated with carbazochrome salicylate.

Originator

Curator's Comment: On Monday, January 05, 1953, a U.S. federal trademark registration was filed for ADRENOSEM (Carbazochrome Sulfonic Acid) by BEECHAM INC., Bristol.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Phosphoinositide hydrolysis
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Unknown

Approved Use

Unknown
Preventing
ADONA

Approved Use

Hemorrhagic tendency (purpura etc.) due to decreased capillary resistance and increased capillary permeability. Hemorrhage from skin, mucous membrane and internal membrane, hemorrhage at eyeground, nephrotic hemorrhage and metrorrhagia. Abnormal bleeding during and after operation due to decrease of capillary resistance.

Launch Date

1955
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Can also be injected intramuscularly, subcutaneously and intravenously http://drugs-infos.blogspot.ru/2009/08/adona.html
In general, for adults, take 10 to 30mg of the active ingredient at a time 3 times a day. The dosage may be adjusted according to disease, age and symptoms of the patient. This preparation contains 30mg of the active ingredient in a tablet.
Route of Administration: Oral
In Vitro Use Guide
0.1-1 M of carbazochrome sulfonic acid reversed the barrier dysfunction induced by tryptase, thrombin and bradykinin in cultured porcine aortic endothelial cells.
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:35:27 GMT 2023
Edited
by admin
on Sat Dec 16 05:35:27 GMT 2023
Record UNII
Y6G4426VGB
Record Status Validated (UNII)
Record Version
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Name Type Language
CARBAZOCHROME SODIUM SULFONATE HYDRATE
JAN  
Common Name English
(±)-CARBAZOCHROME SODIUM SULFONATE TRIHYDRATE
Common Name English
CARBAZOCHROME SODIUM SULFONATE HYDRATE [JAN]
Common Name English
Carbazochrome sodium sulfonate trihydrate [WHO-DD]
Common Name English
MONOSODIUM (2RS)-1-METHYL-6-OXO-5-SEMICARBAZONE-2,3,5,6-TETRAHYDROINDOLE-2-SULFONATE TRIHYDRATE
Common Name English
CARBAZOCHROME SODIUM SULFONATE TRIHYDRATE
WHO-DD  
Common Name English
Code System Code Type Description
DAILYMED
Y6G4426VGB
Created by admin on Sat Dec 16 05:35:27 GMT 2023 , Edited by admin on Sat Dec 16 05:35:27 GMT 2023
PRIMARY
FDA UNII
Y6G4426VGB
Created by admin on Sat Dec 16 05:35:27 GMT 2023 , Edited by admin on Sat Dec 16 05:35:27 GMT 2023
PRIMARY
SMS_ID
100000168997
Created by admin on Sat Dec 16 05:35:27 GMT 2023 , Edited by admin on Sat Dec 16 05:35:27 GMT 2023
PRIMARY
EVMPD
SUB182589
Created by admin on Sat Dec 16 05:35:27 GMT 2023 , Edited by admin on Sat Dec 16 05:35:27 GMT 2023
PRIMARY
RXCUI
2469330
Created by admin on Sat Dec 16 05:35:27 GMT 2023 , Edited by admin on Sat Dec 16 05:35:27 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE