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Merck

119149

ZM 241385

A highly potent, selective, non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells).

Synonym(s):

Adenosine A2A Receptor Antagonist I, ZM 241385

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About This Item

Empirical Formula (Hill Notation):
C16H15N7O2
CAS Number:
139180-30-6
Molecular Weight:
337.34
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
MFCD00908394

Product Name

Adenosine A2A Receptor Antagonist I, ZM 241385, A highly potent, selective, non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells).

SMILES string

[n]21nc(nc2nc(nc1N)NCCc4ccc(cc4)O)c3[o]ccc3

InChI

1S/C16H15N7O2/c17-14-20-15(18-8-7-10-3-5-11(24)6-4-10)21-16-19-13(22-23(14)16)12-2-1-9-25-12/h1-6,9,24H,7-8H2,(H3,17,18,19,20,21,22)

InChI key

PWTBZOIUWZOPFT-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

potency

800 pM Ki

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

color

white

solubility

DMSO: 15 mg/mL

application(s)

air monitoring

compatibility

for use with Viable Air Samplers (1.09191)
for use with Viable Air Samplers (1.09194)
for use with Viable Air Samplers (1.17103)
for use with Viable Air Samplers (1.17274)
for use with Viable Air Samplers (1.17275)

shipped in

ambient

storage temp.

2-8°C

Quality Level

100

Biochem/physiol Actions

Primary Target
A2A
Reversible: yes

Disclaimer

Toxicity: Standard Handling (A)

General description

A highly potent, selective, and orally bioavailable non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells). Does not exhibit any significant antagonistic activity in A1, A2B (Ki = 255 nM and 50 nM, respectively in human adenosine receptors stably expressed in CHO cells) or in A3R (Ki >10 µM in human A3R stably expressed in HEK-293 cells). Shown to have a protective effect against beta-amyloid peptide toxicity.
A highly potent, selective, non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells).

Other Notes

Poucher, S. M., et al. 1995. Brit. J. Pharmacol. 115, 1096.
Ongini, E. et al. 1999. Naunyn Schmiedebergs Arch Pharmacol. 359, 7.

Keddie, J. et al. 1996, Eur Journ Pharm. 301, 107.

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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