Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
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- Epigenetics
-
GPCR/G Protein
- Urotensin Receptor
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Neuro Signaling Pathway
- Imidazoline Receptor
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- mGluR
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Protease/Metabolic Enzyme
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- TGF beta/Smad
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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinoline Series
- Quinazoline
- Pyrazole Series
- Pyrimidine Series
- Boric acid
- Saccharide
- Thiophene Series
- Pyrrole Series
- Indole Series
- Azaindole
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
mGluR
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP33908 | Decoglurant New | 911115-16-7 |
Decoglurant (RO4995819) is a negative allosteric modulator of mGluR2 and mGluR3. Decoglurant is developed as an antidepressant.
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BCP33084 | YM 298198 Hydrochloride New | 748758-45-4 |
YM 298198 Hydrochloride is a non-competitive antagonist with high affinity and selectivity for mGlu1 receptors (Ki = 19 nM).
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BCP33083 | NPS 2390 New | 226878-01-9 |
NPS2390 is a group I mGlu antagonist; displays noncompetitive antagonist activity at both mGlu1 and mGlu5 receptors.
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BCP33034 | SIB 1893 New | 6266-99-5 |
SIB-1893 is a selective non-competitive antagonist of the metabotropic glutamate mGlu5 receptor subtype.
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BCP33033 | SIB 1757 New | 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.
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BCP32664 | GET-73 New | 202402-01-5 |
GET-73 is a mGlu5 receptor allosteric modulator potentially for the treatment of alcoholism.
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BCP32622 | ADX-88178 New | 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.
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BCP25038 | PHCCC New | 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.
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BCP21205 | Eglumetad New | 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.
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BCP27694 | VU-29 New | 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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