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Lavendustin A

Lavendustin A

Product ID L0284
Cas No. 125697-92-9
Purity ≥97%
Product Unit SizeCostQuantityStock
1 mg $156.00 In stock
5 mg $355.00 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

Description

Lavendustin A inhibits various tyrosine kinases and exhibits neuroprotective activity, increasing axonal outgrowth in neurons; this compound is used in research models to examine the effects of tyrosine kinases.

Product Info

Cas No.

125697-92-9

Purity

≥97%

Formula

C21H19NO6

Formula Wt.

381.38

Chemical Name

5-Amino-[(N-2,5-dihydroxybenzyl)-N'-2-hydroxy- benzyl]salicylic Acid

IUPAC Name

5-[(2, 5-dihydroxyphenyl)methyl-[(2-hydroxyphenyl)methyl]amino]-2- hydroxybenzoic acid

Synonym

5-[[(2,5-Dihydroxyphenyl)methyl][(2-hydroxyphenyl)- methyl]amino]-2-hydroxybenzoic acid

Melting Point

158°C

Solubility

Soluble in DMSO or ethanol, or acetic acid.

Appearance

White to off-white crystal

Shipping and Storage

Store Temp

-20°C

Ship Temp

Ambient

Downloads

MSDS

L0284 MSDS PDF

Info Sheet

L0284 Info Sheet PDF

References

Rojas A, Wetherington J, Shaw R, et al. Activation of group I metabotropic glutamate receptors potentiates heteromeric kainate receptors. Mol Pharmacol. 2013 Jan;83(1):106-21. PMID: 23066089.

Kim HJ, Ahn HS, Choi BH, et al. Inhibition of Kv4.3 by genistein via a tyrosine phosphorylation-independent mechanism. Am J Physiol Cell Physiol. 2011 Mar;300(3):C567-75. PMID: 21148405.

Murakami K, Kanno H, Yamamoto I, et al. Lavendustin A enhances axon elongation in VHL gene-transfected neural stem cells. Neuroreport. 2004 Mar 22;15(4):611-4. PMID: 15094462.

Custom Order

  • Size of single unit expressed as number (e.g. '500' in the case of 500 mg)
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