320 Results for "

diphosphate

" in MedChemExpress (MCE) Product Catalog:
Products (320)

320 Results for "diphosphate" in MCE Product Catalog:

  • Targets Recommended:
51
51 Publications Verification
Art. -Nr.: HY-B0445
CAS. Nr.: 53-84-9
Synonyms: β-DPN; β-NAD; β-Nicotinamide Adenine Dinucleotide
NAD+ is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage.
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21
21 Cited Publications
Art. -Nr.: HY-A0129
CAS. Nr.: 51-74-1
Synonyms: Histamine diphosphate
Histamine phosphate is the agonist for histamine receptor and a vasodilator. Histamine phosphate is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine phosphate affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine phosphate can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma .
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14
14 Cited Publications
Art. -Nr.: HY-15592
CAS. Nr.: 1051375-10-0
Reinheit:  99.91%
Synonyms: GSK-1265744; S/GSK1265744
Target:  

OAT HIV HIV Integrase

Forschungsgebiete:  

Infection

Cabotegravir (GSK-1265744) is a orally active and long-acting HIV integrase strand transfer inhibitor and organic anion transporter 1/3 (OAT1/OAT3) inhibitor with IC50 values of 2.5 nM, 0.41 μM and 0.81 μM for HIVADA, OAT3 and OAT1, respectively. Cabotegravir is primarily metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A1, with low potential to interact with other antiretroviral agents (ARVs). Cabotegravir can be used to research AIDS .
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14
14 Cited Publications
Art. -Nr.: HY-15592A
CAS. Nr.: 1051375-13-3
Reinheit:  99.87%
Synonyms: GSK-1265744 sodium; S/GSK1265744 sodium
Target:  

OAT HIV HIV Integrase

Forschungsgebiete:  

Infection

Cabotegravir (GSK-1265744) sodium is a orally active and long-acting HIV integrase strand transfer inhibitor and organic anion transporter 1/3 (OAT1/OAT3) inhibitor with IC50 values of 2.5 nM, 0.41 μM and 0.81 μM for HIVADA, OAT3 and OAT1, respectively. Cabotegravir sodium is primarily metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A1, with low potential to interact with other antiretroviral agents (ARVs). Cabotegravir sodium can be used to research AIDS .
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13
13 Cited Publications
Art. -Nr.: HY-16582
CAS. Nr.: 1218778-77-8
Synonyms: Erismodegib diphosphate; LDE225 diphosphate; NVP-LDE225 diphosphate
Target:  

Smo

Forschungsgebiete:  

Cancer

Sonidegib diphosphate (Erismodegib diphosphate) is a potent and selective Smo antagonist with IC50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectively .
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10
10 Cited Publications
Art. -Nr.: HY-11101
CAS. Nr.: 121268-17-5
Reinheit:  99.6%
Synonyms: Alendronate; MK 217; G-704650 Adronat
Alendronate (sodium hydrate) is a farnesyl diphosphate synthase inhibitor with IC50 of 460 nM.
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9
9 Cited Publications
Art. -Nr.: HY-W010918
CAS. Nr.: 58-64-0
Synonyms: Adenosine diphosphate; ADP
Adenosine 5'-diphosphate (Adenosine diphosphate) is a nucleoside diphosphate. Adenosine 5'-diphosphate is the product of ATP dephosphorylation by ATPases. Adenosine 5'-diphosphate induces human platelet aggregation and inhibits stimulated adenylate cyclase by an action at P2T-purinoceptors.
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9
9 Cited Publications
Art. -Nr.: HY-D0199
CAS. Nr.: 16178-48-6
Synonyms: Adenosine diphosphate disodium; ADP disodium
Adenosine 5'-diphosphate disodium is a nucleoside diphosphate. Adenosine 5'-diphosphate disodium is the product of ATP dephosphorylation by ATPases. Adenosine 5'-diphosphate disodium is a platelet aggregation agent for hemostasis and the development and extension of arterial thrombosis .
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9
9 Cited Publications
Art. -Nr.: HY-W010791
CAS. Nr.: 20398-34-9
Target:  

Endogenous Metabolite

Forschungsgebiete:  

Others

Adenosine 5'-diphosphate sodium salt is a nucleoside diphosphate and the product of ATP dephosphorylation by ATPases. Adenosine 5'-diphosphate sodium salt induces human platelet aggregation and inhibits stimulated adenylate cyclase through its action on P2T-purinergic receptors .
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6
6 Cited Publications
Art. -Nr.: HY-12651
CAS. Nr.: 63-45-6
Reinheit:  99.28%
Synonyms: Primaquine phosphate; Primaquine bisphosphate
Target:  

Parasite

Forschungsgebiete:  

Infection Cancer

Primaquine diphosphate is a potent antimalaria agent and a potent gametocytocide in falciparum malaria. Primaquine diphosphate prevents relapse in vivax and ovale malaria .
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6
6 Cited Publications
Art. -Nr.: HY-100313A
CAS. Nr.: 182959-33-7
Reinheit:  98.23%
Forschungsgebiete:  

Infection Metabolic Disease

YM-53601, a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo . YM-53601 inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. Lipid-lowering agent . YM-53601 is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation .
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5
5 Cited Publications
Art. -Nr.: HY-B0739
CAS. Nr.: 987-78-0
Synonyms: Cytidine diphosphate-choline; CDP-Choline; Cytidine 5'-diphosphocholine
Citicoline is an endogenous intermediate in the synthesis of phosphatidylcholine which is a component of cell membranes. Citicoline inhibits reactive oxygen species (ROS) and apoptosis. Citicoline can be used for neurological disease and hearing loss study .
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5
5 Cited Publications
Art. -Nr.: HY-B0739A
CAS. Nr.: 33818-15-4
Synonyms: Cytidine diphosphate-choline sodium; CDP-Choline sodium; Cytidine 5'-diphosphocholine sodium
Citicoline sodium is an endogenous intermediate in the synthesis of phosphatidylcholine which is a component of cell membranes. Citicoline sodium inhibits reactive oxygen species (ROS) and apoptosis. Citicoline sodium can be used for neurological disease and hearing loss study .
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5
5 Cited Publications
Art. -Nr.: HY-P2764
CAS. Nr.: 9000-95-7
Target:  

NTPDase

Forschungsgebiete:  

Inflammation/Immunology

Apyrase is an Nucleoside triphosphate diphosphohydrolase (NTPDase). Apyrase can hydrolyze extracellular adenosine triphosphate (ATP) and adenosine diphosphate (ADP). Apyrase can inhibit Stx2 toxin release of enterohemorrhagic Escherichia coli (EHEC) infection and protect the intestinal barrier function. Apyrase can be used for the research of infection and inflammation, such as hemorrhagic colitis .
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4
4 Cited Publications
Art. -Nr.: HY-10229
CAS. Nr.: 857876-30-3
Reinheit:  99.86%
Synonyms: AMG 706 diphosphate
Target:  

c-Kit VEGFR

Forschungsgebiete:  

Cancer

Motesanib Diphosphate (AMG 706 Diphosphate) is a potent ATP-competitive inhibitor of VEGFR1/2/3 with IC50s of 2 nM/3 nM/6 nM, respectively, and has similar activity against Kit, and is approximately 10-fold more selective for VEGFR than PDGFR and Ret.
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4
4 Cited Publications
Art. -Nr.: HY-106254A
CAS. Nr.: 1198151-75-5
Reinheit:  98.75%
Synonyms: BTA798 diphosphate
Target:  

Enterovirus

Forschungsgebiete:  

Infection Inflammation/Immunology

Vapendavir diphosphate (BTA798 diphosphate) is a potent enteroviral capsid binder (CB). Vapendavir diphosphate (BTA798 diphosphate) possesses potent antiviral activity for enterovirus 71 (EV71) replication, with EC50 values of 0.5-1.4 μM in different EV71 strains .
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4
4 Cited Publications
Art. -Nr.: HY-19638A
CAS. Nr.: 163706-36-3
Synonyms: AR-C69931MX tetrasodium
Target:  

P2Y Receptor

Cangrelor tetrasodium, an adenosine triphosphate analogue, is a reversible and selective platelet P2Y12 antagonist, with prompt and potent antiplatelet effects. Cangrelor tetrasodium directly blocks adenosine diphosphate (ADP)-induced activation and aggregation of platelets. Cangrelor tetrasodium is also a nonspecific GPR17 antagonist .
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2
2 Cited Publications
Art. -Nr.: HY-113066A
CAS. Nr.: 7415-69-2
Reinheit:  ≥95.0%
Synonyms: GDP disodium salt
Guanosine 5'-diphosphate (GDP) disodium salt, a purine nucleoside diphosphate, is interconverted to guanosine by the action of exonucleotidase and phosphorylation of nucleoside to guanine. Guanosine 5'-diphosphate disodium salt activates adenosine 5'-triphosphate-sensitive K + channel and is used to study the kinetics and characteristics of GTPases such as those associated with G-protein coupled receptors (GPCR). Guanosine 5'-diphosphate disodium salt is a potential iron mobilizer, which prevents the Hepcidin (HY-P70400)-ferroportin interaction and modulates the interleukin-6 (IL-6)/stat-3 pathway. Elevated levels of guanosine 5’-diphosphate are associated with the pathogenesis of neurological diseases. Guanosine 5'-diphosphate disodium salt is promising for the research of inflammation, such as anemia of inflammation (AI) .
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2
2 Cited Publications
Art. -Nr.: HY-W010832
CAS. Nr.: 27821-45-0
Synonyms: UDP disodium salt
Uridine-5'-diphosphate disodium salt is a potent, selective P2Y6 receptor native agonist (EC50=300 nM; pEC50=6.52 for human P2Y6 receptor). Uridine-5'-diphosphate disodium salt, an endogenous metabolite, catalyzes the glucuronidation of a wide array of substrates and is used in nucleic acid (RNA) biosynthesis .
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2
2 Cited Publications
Art. -Nr.: HY-113066C
CAS. Nr.: 43139-22-6
Reinheit:  99.88%
Synonyms: GDP sodium, Type I, 96% (HPLC)
Guanosine 5'-diphosphate (GDP) sodium, 96% (HPLC) is a nucleoside diphosphate that activates adenosine 5'-triphosphate-sensitive K + channel. Guanosine 5'-diphosphate sodium, 96% (HPLC) is an iron mobilizer, which forms a complex with hepcidin to inhibit the hepcidin-ferroportin (FPN) interaction and modulates the IL-6/stat-3 pathway. Guanosine 5'-diphosphate sodium, 96% (HPLC) ameliorates the Turpentine-induced anemia of inflammation (AI) in mice when combined with FeSO4. Guanosine 5'-diphosphate sodium, 96% (HPLC) can be used in the research of AI .
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