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  8. RP 67580, Tocris Bioscience™

RP 67580, Tocris Bioscience™

Catalog Number 163550
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Quantity:
10 mg
50 mg
This item is not returnable. View return policy
135911-02-3
C29H30N2O2
438.571
VWBOQFANCXZMAU-LOSJGSFVSA-N
unii-49u9m41bgy, 7,7-diphenyl-2-1-imino-2-2-methoxyphenyl ethyl perhydroisoindol-4-one, 4h-isoindol-4-one, octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-, 3ar-cis, 3ar,7ar-octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-4h-isoindol, 4h-isoindol-4-one, octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-, 3ar,7ar, tocris-1635, d08kxe, 3ar,7ar-octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-4h-isoindol-4-one, 3ar,7ar-2-1-imino-2-2-methoxy-phenyl-ethyl-7,7-diphenyl-octahydro-isoindol-4-one, 3ar,7ar-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-4-perhydroisoindolone
107686
(3aR,7aR)-2-[2-(2-methoxyphenyl)ethanimidoyl]-7,7-diphenyl-1,3,3a,5,6,7a-hexahydroisoindol-4-one
COC1=CC=CC=C1CC(=N)N2CC3C(C2)C(CCC3=O)(C4=CC=CC=C4)C5=CC=CC=C5
This item is not returnable. View return policy
135911-02-3
C29H30N2O2
438.571
VWBOQFANCXZMAU-LOSJGSFVSA-N
unii-49u9m41bgy, 7,7-diphenyl-2-1-imino-2-2-methoxyphenyl ethyl perhydroisoindol-4-one, 4h-isoindol-4-one, octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-, 3ar-cis, 3ar,7ar-octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-4h-isoindol, 4h-isoindol-4-one, octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-, 3ar,7ar, tocris-1635, d08kxe, 3ar,7ar-octahydro-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-4h-isoindol-4-one, 3ar,7ar-2-1-imino-2-2-methoxy-phenyl-ethyl-7,7-diphenyl-octahydro-isoindol-4-one, 3ar,7ar-2-1-imino-2-2-methoxyphenyl ethyl-7,7-diphenyl-4-perhydroisoindolone
107686
(3aR,7aR)-2-[2-(2-methoxyphenyl)ethanimidoyl]-7,7-diphenyl-1,3,3a,5,6,7a-hexahydroisoindol-4-one
COC1=CC=CC=C1CC(=N)N2CC3C(C2)C(CCC3=O)(C4=CC=CC=C4)C5=CC=CC=C5

Description

Potent and selective NK1 antagonist

Potent and selective tachykinin NK1 receptor antagonist (Ki values are 2.9 nM and > 10 μM for rat NK1, and rat NK2 and NK3 receptors respectively). Displays higher affinity at rat and mouse than human receptors. Antinociceptive in vivo, possibly partly via inhibition of calcium channels.
Quantity 50 mg
Formula Weight 438.57
Percent Purity >97%
Chemical Name or Material RP 67580

Safety and Handling

Recommended Storage Store at -20°C
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