lavendustin A
CAS No. 125697-92-9
lavendustin A( Lavendustin A | RG 14355 | RG-14355 | RG14355. )
Catalog No. M17228 CAS No. 125697-92-9
lavendustin A is a potent, cell-permeable inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 312 | In Stock |
|
| 5MG | 537 | In Stock |
|
| 10MG | 767 | In Stock |
|
| 25MG | 1161 | In Stock |
|
| 50MG | 1557 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Namelavendustin A
-
NoteResearch use only, not for human use.
-
Brief Descriptionlavendustin A is a potent, cell-permeable inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase.
-
DescriptionLavendustin A, also known as RG 14355, is a potent, cell-permeable inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase (IC50 = 11 nM). Lavendustin A shows cytotoxic effects on tumor cell lines. Lavendustin A enhances axon elongation in VHL gene-transfected neural stem cells.
-
In Vitro——
-
In Vivo——
-
SynonymsLavendustin A | RG 14355 | RG-14355 | RG14355.
-
PathwayEndocrinology/Hormones
-
TargetCaMK
-
RecptorEGFR
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number125697-92-9
-
Formula Weight381.38
-
Molecular FormulaC21H19NO6
-
Purity>98% (HPLC)
-
SolubilityDMSO : ≥ 250 mg/mL 655.51 mM
-
SMILESO=C(O)c1cc(N(Cc2cc(O)ccc2O)Cc2ccccc2O)ccc1O
-
Chemical Name5-[[(2,5-Dihydroxyphenyl)methyl][(2-hydroxyphenyl)methyl]amino]-2-hydroxybenzoic acid
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Nam DH, et al. Synthesis and anticancer activity of chromone-based analogs of lavendustin A. Eur J Med Chem. 2010 Sep;45(9):4288-92
molnova catalog
related products
-
SCR7 pyrazine
SCR7 is a specific DNA Ligase IV inhibitor, which blocks nonhomologous end-joining (NHEJ).
-
CAMKK2 inhibitor 4t
CAMKK2 inhibitor 4t is a potent, selective, orally available, brain-penetrant CAMKK2 inhibitor with pIC50 of 8.5.
-
Calmodulin-Dependent...
Calmodulin-Dependent Protein Kinase II (290-309) is a potent CaMK antagonist with an IC50 of 52 nM for inhibition of Ca2+/calmodulin-dependent protein kinase II.
Cart
sales@molnova.com