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Galegine hydrochloride - ≥97.0%, high purity , CAS No.2368870-39-5

    Grade & Purity:
  • ≥97%
In stock
Item Number
G650848
Grouped product items
SKU Size
Availability
Price Qty
G650848-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$200.90
G650848-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$350.90

Alkaloids Other Alkaloids

Basic Description

Specifications & Purity ≥97%
Biochemical and Physiological Mechanisms Galegine hydrochloride, a guanidine derivative, contributes to weight loss in mice. Guanidine hydrochloride is the compound derived from G. officinalis , which gave rise to the biguanides, metformin and phenformin. Galegine hydrochloride activates AMPK in
Storage Temp Store at 2-8°C,Desiccated
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Galegine hydrochloride, a guanidine derivative, contributes to weight loss in mice. Guanidine hydrochloride is the compound derived from G. officinalis , which gave rise to the biguanides, metformin and phenformin. Galegine hydrochloride activates AMPK in 3T3-L1 adipocytes and L6 myotubes, as well as in the H4IIE rat hepatoma and HEK293 human kidney cell lines. Galegine hydrochloride has antibacterial activity, with minimum inhibitory concentration of 4 mg/L against Staphylococcus aureus strains.

In Vitro

Pre-treatment with Galegine hydrochloride (10 μM-3 mM; 5 h) produces a concentration-dependent stimulation of insulin-independent glucose uptake by 3T3-L1 adipocytes without any effect on cell viability. Incubation with Galegine hydrochloride (1 μM-1 mM, 5 h) produces a concentration-dependent stimulation of glucose uptake into L6 myotubes, again without any effect on cell viability. Galegine hydrochloride (0.3-300 μM; 24 hours) produced a slight reduction in basal glycerol release and a more marked reduction in isoprenaline-stimulated glycerol release from 3T3-L1 adipocytes. Incubation of H4IIE rat hepatoma cells with Galegine hydrochloride (10 or 300 μM) for up to 6 hours produces a time-dependent activation of AMPK measured in cell lysates, with maximal activation at 360 min and twofold activation still evident at 24 hous in the presence of 300 μM Galegine hydrochloride. The effect of 300 ΜM Galegine hydrochloride is markedly greater than that of 10 μM. Incubation with Galegine hydrochloride for 1 hour produces a concentration-dependent activation of AMPK in both 3T3L-1 adipocytes and L-6 myotubes. Galegine hydrochloride also produces a concentration-dependent activation of the enzyme in a human kidney cell line (HEK293). MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Galegine hydrochloride (63 mg/kg; feed; daily for 11 days) produces a significant reduction in body weight . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Adult male BALB/c mice Dosage: 63 mg/kg Administration: feed; daily for 11 days Result: Produced a significant reduction in body weight.

Form:Solid

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Guanidines
Intermediate Tree Nodes Not available
Direct Parent Guanidines
Alternative Parents Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Organopnictogen compounds  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as guanidines. These are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.
External Descriptors Not available

Names and Identifiers

IUPAC Name 2-(3-methylbut-2-enyl)guanidine;hydrochloride
INCHI InChI=1S/C6H13N3.ClH/c1-5(2)3-4-9-6(7)8;/h3H,4H2,1-2H3,(H4,7,8,9);1H
InChIKey QORPDBRMGGUYRL-UHFFFAOYSA-N
Smiles CC(=CCN=C(N)N)C.Cl
PubChem CID 139034173
Molecular Weight 163.65

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility H2O : 43.33 mg/mL (264.77 mM; Need ultrasonic) DMSO : 5.2 mg/mL (31.78 mM; Need ultrasonic)

Solution Calculators

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