TG 4-155 structure
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Common Name | TG 4-155 | ||
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CAS Number | 1164462-05-8 | Molecular Weight | 394.46 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C23H26N2O4 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of TG 4-155TG4-155 is a potent, brain-permeant and selective EP2 receptor antagonist with a Ki of 9.9 nM[1][2]. TG4-155 shows low nanomolar antagonist activity against only EP2 and DP1[1]. TG4-155 has an EP2 Schild KB of 2.4 nM and displays 550-4750-fold selectivity for EP2 over EP1, EP3, EP4 and IP, but only 14-fold selectivity against the DP1 receptor[2]. |
Name | (E)- N-(2-(2-methyl-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide |
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Synonym | More Synonyms |
Description | TG4-155 is a potent, brain-permeant and selective EP2 receptor antagonist with a Ki of 9.9 nM[1][2]. TG4-155 shows low nanomolar antagonist activity against only EP2 and DP1[1]. TG4-155 has an EP2 Schild KB of 2.4 nM and displays 550-4750-fold selectivity for EP2 over EP1, EP3, EP4 and IP, but only 14-fold selectivity against the DP1 receptor[2]. |
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Related Catalog | |
Target |
EP2 Receptor:9.9 nM (Ki) |
References |
[2]. Ganesh T. Prostanoid receptor EP2 as a therapeutic target. J Med Chem. 2014 Jun 12;57(11):4454-65. |
Molecular Formula | C23H26N2O4 |
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Molecular Weight | 394.46 |
Exact Mass | 394.18900 |
PSA | 61.72000 |
LogP | 4.19600 |
Storage condition | 2-8℃ |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P280-P305 + P351 + P338-P337 + P313 |
RIDADR | NONH for all modes of transport |
TG4-155 |
(E)-N-(2-(2-methyl-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide |
N-(2-(2-methyl-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide |