Basic information Safety Supplier Related

(R)-ZINC-3573 ((R)-ZINC3573)

Basic information Safety Supplier Related

(R)-ZINC-3573 ((R)-ZINC3573) Basic information

Product Name:
(R)-ZINC-3573 ((R)-ZINC3573)
Synonyms:
  • (3R)-N,N-Dimethyl-1-(5-phenylpyrazolo[1,5-a]pyrimidin-7-yl)-3-pyrrolidinamine
  • (R)-ZINC-3573 ((R)-ZINC3573)
  • ZINC 3573
  • ZINC3573
  • ZINC-3573
  • 3-Pyrrolidinamine, N,N-dimethyl-1-(5-phenylpyrazolo[1,5-a]pyrimidin-7-yl)-, (3R)-
  • (R)-N,N-Dimethyl-1-(5-phenylpyrazolo[1,5-a]pyrimidin-7-yl)pyrrolidin-3-amine
  • (3R)-N,N-dimethyl-1-{5-phenylpyrazolo[1,5-a]pyrimidin-7-yl}pyrrolidin-3-amine
CAS:
2089389-15-9
MF:
C18H21N5
MW:
307.39
Mol File:
2089389-15-9.mol
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(R)-ZINC-3573 ((R)-ZINC3573) Chemical Properties

Density 
1.23±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
8.69±0.20(Predicted)
form 
Solid
color 
Off-white to light yellow
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(R)-ZINC-3573 ((R)-ZINC3573) Usage And Synthesis

Uses

(R)-ZINC-3573 is a selective Mas-related G protein-coupled receptor X2 (MRGPRX2) agonist with an EC50 value of 740 nM. (R)-ZINC-3573 can be used as a MRGPRX2 probe for the research of pain and itch[1].

Biological Activity

(R)-ZINC-3573 is a selective agonist probe of the orphan receptor Mas-related G-protein coupled receptor member X2 (MRGPRX2), a G-protein coupled receptor (GPCR) selectively expressed in mast cells and dorsal root and trigeminal ganglia primary sensory neurons of primates. Lack of selective and potent probes has made it difficult to determine MRGPRX2 funtion. (R)-ZINC-3573 was shown to be a potent and selective agonist with an EC50 value of 760 nM for MRGPRX2 and little activity for MRGPRX1 or over 350 other GPCRs and 97 kinases tested. (R)-ZINC-3573 activates endogenous MRGPRX2 expressed in a human mast cell line and induced degranulation and calcium release. (S)-ZINC-3573 is inactive and can be used as a control.

storage

Store at +4°C

References

[1] Lansu K, et al. In silico design of novel probes for the atypical opioid receptor MRGPRX2. Nat Chem Biol. 2017 May;13(5):529-536. DOI:10.1038/nchembio.2334

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