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mGluR

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mGluR

Chemical Structure Cat. No. Product Name CAS No.
Decoglurant Chemical Structure
BCP33908 Decoglurant 911115-16-7
Decoglurant (RO4995819) is a negative allosteric modulator of mGluR2 and mGluR3. Decoglurant is developed as an antidepressant.
YM 298198 Hydrochloride Chemical Structure
BCP33084 YM 298198 Hydrochloride 748758-45-4
YM 298198 Hydrochloride is a non-competitive antagonist with high affinity and selectivity for mGlu1 receptors (Ki = 19 nM).
NPS 2390 Chemical Structure
BCP33083 NPS 2390 226878-01-9
NPS2390 is a group I mGlu antagonist; displays noncompetitive antagonist activity at both mGlu1 and mGlu5 receptors.
SIB 1893 Chemical Structure
BCP33034 SIB 1893 6266-99-5
SIB-1893 is a selective non-competitive antagonist of the metabotropic glutamate mGlu5 receptor subtype.
SIB 1757 Chemical Structure
BCP33033 SIB 1757 31993-01-8
SIB-1757 is a highly selective antagonist for the mGlu5 metabotropic glutamate receptor subtype. SIB-1757 displays an IC50 value of 0.4 μM at hmGlu5 compared with > 30 μM at hmGlu1b, hmGlu2, hmGlu4, hmGlu6, hmGlu7 and hmGlu8.
GET-73 Chemical Structure
BCP32664 GET-73 202402-01-5
GET-73 is a mGlu5 receptor allosteric modulator potentially for the treatment of alcoholism.
ADX-88178 Chemical Structure
BCP32622 ADX-88178 1235318-89-4
ADX88178 is a potent metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM) with an EC50 of 4 nM for human mGluR4.
PHCCC Chemical Structure
BCP25038 PHCCC 179068-02-1
PHCCC is a Group I metabotropic glutamate receptor antagonist with EC 50 of 6 uM and a positive allosteric modulator of mGluR4. Also as a potent to antagonism for mGluR2 and mGluR8.
Eglumetad Chemical Structure
BCP21205 Eglumetad 176199-48-7
Eglumegad is a highly potent and selective group II (mGlu2/3) receptor agonist with IC50s of 5 and 24 nM on transfected human mGlu2 and mGlu3 receptors, respectively.
VU-29 Chemical Structure
BCP27694 VU-29 890764-36-0
VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); binds to the MPEP allosteric site (Ki app = 244 nM).
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