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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3595 | Resmetirom | VIA-3196,MGL3196 | Thyroid hormone receptor(THR) |
Resmetirom (VIA-3196) is a highly selective thyroid hormone receptor β (THR-β) agonist. | |||
T7688 | 4-Nonylphenylboronic acid | FAAH | |
4-Nonylphenylboronic acid is a inhibitor of FAAH. | |||
T9970 | mGluR3 modulator-1 | 1-ethyl-3-(morpholin-4-yl)-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile | GluR |
mGluR3 modulator-1 (1-ethyl-3-(morpholin-4-yl)-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile) is a positive allosteric modulator of mGluR3 and can be used in studies about the treatment of Parkinson's disease. | |||
T12717 | Basimglurant | CTEP Derivative,RG7090 | GluR |
Basimglurant (CTEP Derivative) is a potent, selective and orally available modulator of mGlu5 negative allosteric(Kd of 1.1 nM). | |||
T60882 | mGluR2 modulator 2 | ||
mGluR2 modulator 2 (compound 2) can be used in antipsychotic research. mGluR2 modulator 2 is a potent, selective and orally bioavailable positive allosteric modulator of mGluR2 with an EC 50 value of 0.13 μM [1]. | |||
T61277 | mGluR2 modulator 4 | ||
mGluR2 modulator 4 (compound 47) is a highly potent positive allosteric modulator of mGluR2, exhibiting an EC 50 value of 0.8 μM. It holds the potential for investigating antipsychotic properties [1]. | |||
T38910 | mGluR2 antagonist 1 | ||
mGluR2 antagonist 1 is a potent and selective class of negative allosteric modulator targeting the metabotropic glutamate receptor 2 (mGluR2) with high oral bioavailability. It displays a remarkable affinity for mGluR2, ... | |||
T81801 | mGluR5 antagonist-1 | ||
mGluR5 antagonist-1 (compound 10) is a potent mGluR5 inhibitor exhibiting an IC50 of 11.5 nM and demonstrates antidepressant effects [1]. | |||
T62202 | mGluR2 modulator 1 | ||
mGluR2 modulator 1 (compound 95) is a potent, blood-brain-barrier permeable modulator of mGluR2 (metabotropic glutamate receptor-2) positive transmutation (EC50: 0.03 μM). mGluR2 modulator 1 can be used in the study of p... | |||
T38659 | mGluR5 modulator 1 | ||
mGluR5 modulator 1 is a compound that acts as a positive allosteric modulator of the metabotropic glutamate receptor subtype 5 (mGluR5). Its primary application lies in the field of schizophrenia and cognitive impairment... | |||
T74287 | MGlc-DAG | ||
MGlc-DAG, a glycoglycerolipid, serves as a precursor in the synthesis of drug delivery compounds [1]. | |||
T61775 | mGlu4 receptor agonist 1 | ||
mGlu4 receptor agonist 1 (compound 62) is a highly effective positive allosteric modulator of mGlu4 receptors, displaying an EC 50 of 308 nM. Additionally, it exhibits noteworthy anxiolytic and antipsychotic properties [... | |||
T3591 | URB602 | Lipase , Antibacterial | |
URB602 is a specific monoacylglycerol lipase (MGL) inhibitor, which inhibits rat brain MGL (IC50: 28±4 μM) through a noncompetitive mechanism. | |||
T28165 | NF-1819 | NF 1819,NF1819 | Lipase |
NF-1819 is a potent and selective irreversible MGL (β-lactam-based monoacylglycerol lipase) inhibitor. NF-1819 alleviates symptoms in a MS model in vivo and exhibits analgesic effects in an acute inflammatory pain model ... | |||
T5737 | Euphol | Others , Lipase , Endogenous Metabolite | |
Euphol, an alcohol tetracyclic triterpene, has a wide range of pharmacological properties and is considered to have anti-inflammatory action. | |||
T4S1050 | Pristimerin | Celastrol methyl ester | NF-κB , Antibacterial |
1. Pristimerin (Celastrol methyl ester) has anticancer activity , treatment with Pristimerin may be a potential strategy for the suppression of hypoxia-induced metastasis through the reversal of hypoxia-induced stem cell... | |||
T71493 | AM6580 | ||
AM6580 is an irreversible monoacylglycerol lipase (MGL) inhibitor. | |||
T34521 | SAR629 | SAR 629,SAR-629 | |
SAR-629 is an MGL inhibitor or 2-AG degradation inhibitor. | |||
T61294 | Monoacylglycerol lipase inhibitor 1 | ||
Monoacylglycerol lipase inhibitor 1, also known as compound 13 [1], is a potent inhibitor of monoacylglycerol lipase. |