Basic information Safety Supplier Related

HNMPA-(AM)3

Basic information Safety Supplier Related

HNMPA-(AM)3 Basic information

Product Name:
HNMPA-(AM)3
Synonyms:
  • PRO-DRUG II
  • HYDROXY-2-NAPHTHALENYLMETHYLPHOSPHONIC ACID TRISACETOXYMETHYL ESTER
  • HNMPA-(AM)
  • HNMPA-(AM)3
  • Phosphonic acid, P-[[(acetyloxy)methoxy]-2-naphthalenylmethyl]-, bis[(acetyloxy)methyl] ester
  • HNMPA-(AM)3
CAS:
120944-03-8
MF:
C20H23O10P
MW:
454.36
Mol File:
Mol File
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HNMPA-(AM)3 Chemical Properties

Boiling point:
573.1±50.0 °C(Predicted)
Density 
1.325±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
DMF: 15 mg/ml; DMSO: 1 mg/ml; Ethanol: 25 mg/ml; PBS (pH 7.2): 1 mg/ml
form 
Colorless oil.
color 
Colorless to light yellow
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HNMPA-(AM)3 Usage And Synthesis

Uses

HNMPA-(AM)3 is a cell-permeable and selective insulin receptor tyrosine kinase inhibitor analog of HNMPA. HNMPA-(AM)3 greatly inhibits the ability of prothoracicotropic hormone (PTTH) to activate ERK phosphorylation and stimulate ecdysteroidogenesis. HNMPA-(AM)3 is also effective in inhibiting ecdysteroid production (IC50=14.2 μM) and insulin receptor activity (IC50 is 14.2 μM and 200 μM in mosquitoes and mammals, respectively)[1][2].

Definition

ChEBI: Hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester is an organic phosphonate that is the trisacetoxymethylester derivative of naphthalene substituted hydroxymethylphosphonic acid. It has been found to inhibit insulin receptor tyrosine kinase activity and insulin stimulated glucose oxidation. It has a role as a tyrosine kinase inhibitor. It is an organic phosphonate, a member of naphthalenes and an acetate ester. It is functionally related to a hydroxymethylphosphonic acid.

Biological Activity

Cell permeable: yes', 'Primary Target
tyrosine kinase', 'Product does not compete with ATP.', 'Reversible: no', 'Target IC50: 100 μM and 10 μM against insulin receptor tyrosine kinase and insulin-stimulated glucose oxidation in isolated r at adipocytes, respectively

References

[1] Riehle MA, et al. Insulin stimulates ecdysteroid production through a conserved signaling cascade in the mosquito Aedes aegypti. Insect Biochem Mol Biol. 1999 Oct;29(10):855-60. DOI:10.1016/s0965-1748(99)00084-3
[2] Gu SH, et al. PTTH-stimulated ERK phosphorylation in prothoracic glands of the silkworm, Bombyx mori: role of Ca2+/calmodulin and receptor tyrosine kinase. J Insect Physiol. 2010;56(1):93-101. DOI:10.1016/j.jinsphys.2009.09.008

HNMPA-(AM)3Supplier

Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Email
info@efebio.com
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
RD International Technology Co., Limited
Tel
18024082417
Email
market@ubiochem.com
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Enzo Biochem Inc
Tel
Enzo Biochem Inc. 13797054060
Email
Enzoname@qq.com
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