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Substance Name: Stibamine glucoside [INN:BAN]
RN: 1344-34-9
UNII: WXW6I2Y86R
InChIKey: CTZKOPZYANZEBA-PLJZAMQKSA-M

Classification Codes

  • Drug / Therapeutic Agent
  • Organometallic

Molecular Formulas

  • C36-H49-N3-Na-O22-Sb3
  • C36-H49-N3-O22-Sb3.Na

Molecular Weight

  • 1264.05
 
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Names and Synonyms

Name of Substance

  • Stibamine glucoside [INN:BAN]

Synonyms

  • Estibamina-glucosido
  • Estibamina-glucosido [INN-Spanish]
  • Glucostibamine sodium
  • Glucostimidine sodium
  • Neostam stibamine glucoside
  • Nitrogen glucoside of sodium p-aminophenylstibonate
  • Sodium p-aminobenzenestibonate glucoside
  • Sodium stibanilate glucoside
  • Stibamina glucoside
  • Stibamina glucoside [DCIT]
  • Stibamine glucoside
  • Stibamini glucosidum
  • Stibamini glucosidum [INN-Latin]
  • UNII-WXW6I2Y86R

Systematic Names

  • N-Glucoside of sodium 4-aminobenzenestibonate
  • Neostam

Registry Numbers

CAS Registry Number

  • 1344-34-9

FDA UNII

  • WXW6I2Y86R

System Generated Number

  • 0001344349

Molecular Formulas

Molecular Formulas

  • C36-H49-N3-Na-O22-Sb3
  • C36-H49-N3-O22-Sb3.Na

Molecular Formula Fragments

  • C36-H49-N3-O22-Sb3
  • COMPONENT
  • Na

Structure Descriptors

InChI

1S/3C12H16NO5.Na.H2O.6O.3Sb/c3*14-6-8-9(15)10(16)11(17)12(18-8)13-7-4-2-1-3-5-7;;;;;;;;;;;/h3*2-5,8-17H,6H2;;1H2;;;;;;;;;/q;;;+1;;;;;;;-1;;;+1/p-1/t3*8-,9-,10+,11-,12-;;;;;;;;;;;/m111.........../s1

InChIKey

CTZKOPZYANZEBA-PLJZAMQKSA-M

Smiles

N([C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO)c1ccc([Sb@@](O[Sb@@](c2ccc(cc2)N[C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)(=O)O)(=O)O[Sb](=O)([O-])c2ccc(N[C@@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)CO)cc2)cc1.[Na+]

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 1475mg/kg (1475mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 81, Pg. 224, 1944.
rabbit LD50 intramuscular 91mg/kg (91mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) Journal of Pharmacology and Experimental Therapeutics. Vol. 87, Pg. 119, 1946.