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Products starting with 'D'

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

D011-2120 is an antiviral agent. It acts by blocking microtubule polymerization, d...

D153249 is a promoter of spinal muscular atrophy (SMA).

D 15413 has an inhibitory effect on estrogen-dependent mammary tumors.

D 15414 is a nonsteroidal weak estrogen of the 2-phenylindole group which was neve...

D159687 is a selective negative allosteric modulator (NAM) of PDE4D.

D 2097 is a bioactive chemical.

D21-2393 is known as Edoxaban 4-Carboxylic Acid. Subjects received a single-oral-d...

D21-6076 is a β-1,6-Glucan inhibitor. These inhibitors work as antifungal drugs by...

D 2343 is a Beta 2-adrenoreceptor agonist with alpha 1-adrenoreceptor blocking pro...

D264-0698 is a novel ERK2 inhibitor.

D2923 is a selective inhibitor of colony-stimulating factor 1 receptor (CSF1R).

D-2-Aminoglutarimide HCl

D-2-Aminoglutarimide is a synthetic intermediate. It has been used in the synthesi...

d2T is a nucleoside analog of thymidine that has antiviral activity. It inhibits H...

D3-2 is a highly potent S1P1 modulator with apparent pathway selectivity for β-arr...

D-3263 free base

D-3263 is a TRPM8 agonist ( transient receptor potential melastatin member 8) with...

D36 is an androgen receptor (AR) allosteric antagonist with inverse agonist proper...

D44 is an inhibitor of Plasmodium FKBPs.

D-4418, is PDE4 inhibitors has been in development as a novel anti-inflammatory th...

D-4476, also known as Casein Kinase I Inhibitor, is a potent, selective and cell-p...

D-473 is a novel orally active triple reuptake inhibitor targeting dopamine, serot...

D4DAP is HIV virus replication inhibitor.

D4-Ribavirin

D4-Ribavirin is isolated from the brine shrimp active fraction of the MeOH extract...

D-528 is a novel potent triple reuptake inhibitor (DAT: Ki=7.94 nM; NET: Ki=14.6 n...

D-544 is a novel potent triple reuptake inhibitor (DAT: Ki=29.6 nM; NET: Ki=2.14 n...

D54 naponate

D54 naponate is a repository salt form of the biologically active dihydnotniazine,...

D561-0775 is a direct AMPK agonist, showing potential anti-cancer activity via ind...

D595 (10(-5) M), is a phenethylamine-type calcium channel blocker. The most potent...

D5D-IN-326 is a novel Selective Inhibitor of Delta-5 Desaturase (D5D), Lowering In...

D-609, also known as D-609 free, is a phospholipase C inhibitor potentially for th...

D-64131 is a potent and selective tubulin inhibitor. D-64131 inhibits tumor cell p...

D-703 is a bioactive chemical.

D714 is a weakly conserved palm-subdomain residue (located distant from the cataly...

D719 is a novel inhibitor of integrase nuclear translocation, showing significant ...

D-7193, also known as N,N-Diacetylcystine, is an immunosuppressant potentially for...

D 729 is a biochemical.

D75-4590 is a β-1,6-Glucan inhibitor. These inhibitors work as antifungal drugs by...

D77 functions as a novel anti-HIV-1 inhibitor targeting the interaction between in...

D-87503 is a dual extracellular signaling-related kinase (ERK)/PI3K inhibitor.

DA-11004 is a synthetic, potent NADP-dependent isocitrate dehydrogenase (IDPc) inh...

DA 1131 is a new carbapenem antibiotic, undergoes renal metabolism by renal dehydr...

DA 1686 is a therapeutic agent of anti-arrhythmic.

DA-3003-2 is a Cdc25 dual-specific protein tyrosine phosphatase inhibitor. Cdc25 d...

DA 3505 is one of feprazone metabolite. Limits of detection are 0.1 microgram fep...

DA-3934 is of phenoxyacetanilide derivatives, it has high affinity for gastrin/CCK...

DA 4360 is H2-receptor antagonism. The compounds which were investigated in a wide...

DA 4626 is H2-receptor antagonism. The compounds which were investigated in a wide...

DA 4643 is one of histamine H2-receptor antagonistic. Two histamine H2-receptor an...

DA 5018 is a capsaicin derivative, it has the antipruritic effect. DA 5018 is also...

DA-6886 is a 5-Hydroxytryptamine receptor 4 (5-HT4) agonist potentially for the tr...

DA-7867 is a novel oxazolidinone. In vitro activities of DA-7867 were compared to ...