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CAS No 357-70-0 , Galanthamine

  • Name: Galanthamine
  • Synonyms: (-)-Galanthamine;Galanthamine; Galanthaminum; Galantamin; Lycoremin; Galantamine; Reminyl; Galantamina; Jilkon; Lycoremine;galanthamine;
  • CAS Registry Number:
  • Melting Point: 119-1210C
  • Density: 1.28 g/cm3
  • Molecular Weight: 287.35354
  • InchiKey: ASUTZQLVASHGKV-JDFRZJQESA-N
  • InChI: InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11
    (10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1
  • Molecular Formula: C17H21NO3
  • Molecular Structure:CAS No:357-70-0 Galanthamine
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357-70-0 Galanthamine

  • Galanthamine Galanthamine is a long-acting, centrally active acetylcholinesterase(AChE) inhibitor (IC50 = 410 nM) and allosteric potentiator at neuronal nicotinic ACh receptors. Target: JAK Product Links: http://www.medchemexpress.cn/galanthamine.htm...
  • United States MedChemexpress LLC [Manufacturer]
  • Tel: 609-228-6898
  • Fax: --
  • Address: 18 Wilkinson Way, Princeton, NJ 08540, USA Princeton,New JerseyUnited States
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357-70-0 GALANTAMINE

  • Hong kong Advanced Technology & Industrial Co., Ltd. [Manufacturer]
  • Tel: (852) 2390 2293/ (852) 2394 5546
  • Fax: (852) 2789 8314
  • Address: Unit B, 1/F., Cheong Shing Bldg.,
    17 Walnut St., Tai Kok Tsui, Kln,
    Hong Kong null,nullHong kong
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357-70-0 Galantamine

  • IUPAC NAME-(4aS,6R,8aS)- 5,6,9,10,11,12- hexahydro- 3-methoxy- 11-methyl- 4aH- [1]benzofuro[3a,3,2-ef] [2] benzazepin- 6-ol MOLECULAR FORMULA-C17H21NO3 MOLAR MASS-287.354 g/mol Galantamine is used for the treatment of mild to moderate Alzheimer's dis...
  • India Swapnroop Drugs & Pharmaceuticals [Manufacturer, Trading Company]
  • Tel: 91-240-6641875
  • Fax: 91-240-6641875
  • Address: Harsool Aurangabad,MaharashtraIndia

357-70-0 Galanthamine base

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357-70-0 Galanthamine base

  • United States HBCChem, Inc. [Manufacturers]
  • Tel: +1-510-219-6317
  • Fax: +1-510-675-0318
  • Address: null Union City,CaliforniaUnited States
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357-70-0 Galanthamine

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357-70-0 Galanthamine base

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357-70-0 Galantamine

  • China Xingcheng Chempharm Co., Ltd [Manufacturer]
  • Tel: +86-576-88525005/ +86-576-88886292
  • Fax: +86-576-88225056
  • Address: B Area, 10F, Yaoda Mansion, 289, Shifu Road, Taizhou, Zhejiang, China 318000 null,nullChina
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357-70-0 Galantamine

  • India Triveni Chemicals null
  • Tel: +91-(260)-2400022, 3258683
  • Fax: +91-(260)-2400022/3264008
  • Address: 135, Pancharatna, Char Rasta, G.I.D.C., Vapi, Gujarat 396 195, null,nullIndia
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357-70-0 GALANTHAMINE-D3 HYDROBROMIDE

  • India VARDA Biotech (P) Ltd. [Manufacturer]
  • Tel: +91-22-6693 5686 / 2673 0141 / 2673 4258
  • Fax: +91-22-6693 5687
  • Address: 110 & 111, Kartik Complex
    New link Road, Andheri-(W)
    Mumbai-400053, INDIA. null,nullIndia
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References of Galanthamine
Title: Galantamine
CAS Registry Number: 357-70-0
CAS Name: (4aS,6R,8aS)-4a,5,9,10,11,12-Hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol
Synonyms: galanthamine; lycoremine
Molecular Formula: C17H21NO3
Molecular Weight: 287.35
Percent Composition: C 71.06%, H 7.37%, N 4.87%, O 16.70%
Literature References: Selective acetylcholinesterase inhibitor. Isoln from Caucasian snowdrops, Galanthus woronowii Vel., Amaryllidaceae: N. F. Proskurnina, A. P. Yakovleva, J. Gen. Chem. USSR 22, 1899 (1952); from Narcissus spp: Boit et al., Ber. 90, 725, 2197 (1957). Structure work: S. Kobayashi et al., Chem. Ind. (London) 1956, 177. Synthesis and stereochemistry: D. H. R. Barton, G. W. Kirby, Proc. Chem. Soc. London 1960, 392; eidem, J. Chem. Soc. 1962, 806. Asymmetric synthesis of isomers from L-tyrosine: K. Shimizu et al., Heterocycles 8, 277 (1977). Biosynthesis studies: D. H. R. Barton et al., J. Chem. Soc. 1963, 4545; W. D?bke, Heterocycles 6, 551 (1977). Toxicology study: S. L. Friess et al., Toxicol. Appl. Pharmacol. 3, 347 (1961). Clinical pharmacokinetics: U. Bickel et al., Clin. Pharmacol. Ther. 50, 420 (1991). Review of pharmacology: A. L. Harvey, Pharmacol. Ther. 68, 113-128 (1995); of clinical experience in Alzheimer's disease: R. Bullock, Exp. Rev. Neurother. 4, 153-163 (2004); of synthesis and pharmacology: J. Marco-Contelles et al., Chem. Rev. 106, 116-133 (2006).
Properties: Crystals from benzene, mp 126-127°. [a]D20 -118.8° (c = 1.378 in ethanol). Monoacidic base. Fairly sol in hot water; freely sol in alcohol, acetone, chloroform. Less sol in benzene, ether.
Melting point: mp 126-127°
Optical Rotation: [a]D20 -118.8° (c = 1.378 in ethanol)
 
Derivative Type: Hydrochloride
Molecular Formula: C17H21NO3.HCl
Molecular Weight: 323.81
Percent Composition: C 63.06%, H 6.85%, N 4.33%, O 14.82%, Cl 10.95%
Properties: Crystals from water, dec 256-257°. Sparingly sol in cold, more sol in hot water. Very sparingly sol in alcohol, acetone.
 
Derivative Type: Hydrobromide
CAS Registry Number: 1953-04-4
Trademarks: Nivalin (Waldheim); Razadyne (J & J); Reminyl (J & J)
Molecular Formula: C17H21NO3.HBr
Molecular Weight: 368.27
Percent Composition: C 55.44%, H 6.02%, N 3.80%, O 13.03%, Br 21.70%
Properties: Crystals from water, dec 246-247°. [a]D20 -93.1° (c = 0.1015 in 15 ml H2O). Sparingly sol in water. LD50 i.v. in mice (mg/kg): 5.2 ± 0.2 (Friess).
Optical Rotation: [a]D20 -93.1° (c = 0.1015 in 15 ml H2O)
Toxicity data: LD50 i.v. in mice (mg/kg): 5.2 ± 0.2 (Friess)
 
Therap-Cat: Cholinesterase inhibitor.
Keywords: Cholinesterase Inhibitor.