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345670

Galanthamine, Hydrobromide

A competitive and reversible inhibitor of acetylcholinesterase.

Synonym(s):

Galanthamine, Hydrobromide, Nivalin, HBr

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Size/SKUAvailabilityPrice
20 mg

Available to ship TODAYfromAreál Kühne+Nagel spol. s r.o.

CZK 3,920.00

About This Item

Empirical Formula (Hill Notation):
C17H21NO3 · xHBr
CAS Number:
Molecular Weight:
287.35 (free base basis)
MDL number:
UNSPSC Code:
12352116
NACRES:
NA.77
Assay:
≥95% (HPLC)
Form:
solid
Storage condition:
OK to freeze, desiccated

CZK 3,920.00


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Quality Segment

description

Merck USA index - 14, 4340

assay

≥95% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, desiccated

color

white

solubility

ethanol: 1 mg/mL, water: 1 mg/mL, DMSO: 5 mg/mL

shipped in

ambient

storage temp.

2-8°C

SMILES string

[Br-].[N+H]1(CC[C@@]32[C@@H](Oc4c3c(ccc4OC)C1)C[C@H](C=C2)O)C

InChI

1S/C17H21NO3.BrH/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;1H/t12-,14-,17-;/m0./s1

InChI key

QORVDGQLPPAFRS-XPSHAMGMSA-N

General description

A competitive and reversible inhibitor of acetylcholinesterase. Antimyasthenic agent. Can partially reverse the effects of scopolamine-induced amnesia in rats. Reported to improve learning and short-term memory in animal models.
Cholinesterase antagonist. Antimyasthenic agent. Can partially reverse the effects of scopolamine-induced amnesia in rats.

Biochem/physiol Actions

Cell permeable: no
Primary Target
Acetylcholinesterase
Product competes with ATP.
Reversible: yes

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Pilger, C., et al. 2001. J. Mol. Graph. Model19, 288.
Iliev, A., et al. 1999. Methods Find. Exp. Clin. Pharmacol. 21, 297.
Southan, G.J., et al. 1996. Br. J. Pharmacol.117, 619.
Mutafova-Yambolieva, V.N., et al. 1993. Gen. Pharmacol. 24, 1253.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Toxic (F)

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This Item
G1660SML0398PHR1623
form

solid

form

powder

form

powder

form

-

assay

≥95% (HPLC)

assay

≥94% (HPLC)

assay

≥96% (HPLC)

assay

-

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

300

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-30°C

solubility

ethanol: 1 mg/mL, DMSO: 5 mg/mL, water: 1 mg/mL

solubility

DMSO: soluble 10 mg/mL, clear, colorless, water: soluble 20 mg/mL, clear, colorless

solubility

H2O: 5 mg/mL (warmed; clear solution)

solubility

-


pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Certificates of Analysis (COA)

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