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or product name starting with: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

JBP485 is an inhibitor of renal transporters OAT1 and OAT3. JBP485 is an antihepat...

JBSNF-000088

JBSNF-000088 is an inhibitor of Nicotinamide N-methyltransferase (NNMT) for the tr...

JBSNF-000567

JBSNF-000567 is a Metabolite of JBSNF-000088.

JC 1 can be used in a probe for measuring mitochondrial membrane potential by flow...

JC124 is a NLRP3 Inflammasome Inhibitor.

JC1-40 is a novel RORα activator, diminishing diethylnitrosamine-induced acute liv...

JC-171 is an NLRP3 inflammasome inhibitor with biological activity in vivo, for po...

JC 40 is a bioactive chemical.

JCC76 is a selective inhibitor of heat shock protein 27 (Hsp27). JCC76 inhibits th...

JC-D7 is a selective fluorescent probe for specific labeling of synthetic polyP in...

JC-D8 is a novel selective fluorescent probe for specific labeling of synthetic po...

JCF 109 is a bioactive chemical.

Jci 3661 kills mouse mammary tumor FM3A (F28-7) cells.

JCN037 is a potent brain-penetrant EGFR tyrosine kinase inhibitor against malignan...

JCP-170 is an inhibitor of ABHD6 that works in a dose-dependent manner.

JCP174 is an inhibitor of a depalmitoylase that enhances Toxoplasma host-cell inva...

JCP174-Et is a suicide substrate for serine proteases, irreversibly inactivating h...

JCP251 is an inhibitor of serine hydrolases which also acts as a gamma-secretase i...

JCP-265 is an inhibitor of ABHD6 that works in a dose-dependent manner.

JCP405 is a covalent dual inhibitor of DPAP1 and DPAP3.

JCP410 is a covalent dual inhibitor of DPAP1 and DPAP3.

JCP678 is an irreversible serine hydrolases inhibitor.

JD5037 is a peripherally restricted (PR) cannabinoid-1 receptor blocker (CB1R anta...

Jdr 004 is a bioactive chemical.

JDTic dihydrochloride

JDTic dihydrochloride is a kappa opioid receptor (KOR) antagonist that prevents st...

JE-2147 belongs to the class of organic compounds known as hybrid peptides. These ...

JE-2178 is a highly bioavailable compound.

Jedi2 is a Piezo1 channel activator that promotes Ca2+ influx into HEK293 cells ex...

Jegosapogenol A

Jegosapogenol A is a member of the class of compounds known as triterpenoids. Trit...

Jervine HCl

Jervine (11-Ketocyclopamine) is a naturally occuring steroidal alkaloid, and is de...

Jesaconitine

Jesaconitine is an Aconitine analog. Aconitine alkaloid pharmacokinetic analgesic....

JF549,SE (JF549,NHS) is a fluorescent dye with the absorption maximum (λab (max)) ...

JFD00950 is a human flap endonuclease 1 (FEN1) inhibitor with in vitro inhibition ...

JF-NP-26 is a caged raseglurant, releasing raseglurant upon exposure to violet 405...

JG-231 is an allosteric inhibitor of protein-protein interactions with heat shock ...

JG2-38 is a novel inhibitor of the heat shock protein 70 (Hsp70) with anti-prolife...

JG26 is an ADAM17 inhibitor. JG26 also inhibits AngII-induced EGFR transactivation...

JG 365 is a HIV protease inhibitor.

JG-48 is an inhibitor of Hsp70. JG-48 suppresses phosphorylated and total Tau in T...

JG-98, an allosteric heat shock protein 70 (Hsp70) inhibitor, which binds tightly ...

JH295 is an irreversible, cysteine-targeted inhibitors of the human centrosomal ki...

JH-II-127 is a potent and selective inhibitor of both wild-type and G2019S mutant ...

JH-IX-179 is a novel type I ATP competitive, extremely potent and selective FLT3 ...

JHN76359, also known as Slingshot inhibitor D3, is a novel Potent Inhibitor of the...

JH-T4 is a novel sirt2 inhibitor, increasing intracellular k-ras4a lysine fatty a...

JHU-083 is a Glutamine antagonist, a DON prodrug.

JHU 37152 is a high affinity and highly potent activator of hM3Dq and hM4Di DREADD...

JHU 37160 is a high affinity and highly potent activator of hM3Dq and hM4Di DREADD...

JHU395 is a novel orally-bioavailable GA prodrug designed to circulate inert in pl...

JHU-58 is a novel dipeptide MrgC agonist. JHU-58 inhibited both mechanical and he...