1470 Results for "

synthase

" in MedChemExpress (MCE) Product Catalog:
Products (1470)

1470 Results for "synthase" in MCE Product Catalog:

119
119 Publications Verification
Art. -Nr.: HY-N6782
CAS. Nr.: 1404-19-9
Oligomycin, an antifungal antibiotic, is an inhibitor of H +-ATP-synthase. Oligomycin blocks oxidative phosphorylation and the electron transport chain. Oligomycin inhibits HIF-1alpha expression in hypoxic tumor cells .
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86
86 Cited Publications
Art. -Nr.: HY-114180
CAS. Nr.: 2262452-06-0
Reinheit:  99.95%
Synonyms: RU320521
Forschungsgebiete:  

Metabolic Disease

RU.521 (RU320521) is a potent and selective cyclic GMP-AMP synthase (cGAS) inhibitor and inhibits cGAS-mediated interferon upregulation. RU.521 suppresses dsDNA-activated reporter activity with an IC50 of 0.7 μM. RU.521 reduces constitutive expression of interferon in macrophages from a mouse model of Aicardi-Goutières syndrome (AGS) .
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56
56 Cited Publications
Art. -Nr.: HY-14881A
CAS. Nr.: 845533-86-0
Reinheit:  99.97%
Synonyms: R403323; TMC207 fumarate; R207910 fumarate
Target:  

Bacterial Antibiotic

Forschungsgebiete:  

Infection

Bedaquiline fumarate, a diarylquinoline antibiotic that targets ATP synthase, is effective for the treatment of Mycobacterium tuberculosis infections.
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56
56 Cited Publications
Art. -Nr.: HY-14881
CAS. Nr.: 843663-66-1
Reinheit:  99.98%
Synonyms: TMC207; R207910
Target:  

Bacterial Antibiotic

Forschungsgebiete:  

Infection

Bedaquiline (TMC207) is a diarylquinoline agent and inhibits Mycobacterium tuberculosis (Mtb) F1FO-ATP synthase through targeting of both the c- and the ε-subunit . Bedaquiline has uncoupler activity. Bedaquiline is used for the multi-agent resistant tuberculosis .
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52
52 Cited Publications
Art. -Nr.: HY-12364
CAS. Nr.: 218137-86-1
Reinheit:  99.91%
C75 is a synthetic fatty-acid synthase (FASN) inhibitor; inhibits prostate cancer cells PC3 with an IC50 of 35 μM . C75 is a potent CPT1A activator .
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40
40 Cited Publications
Art. -Nr.: HY-10820B
CAS. Nr.: 357166-29-1
Reinheit:  99.46%
Synonyms: LY231514 disodium heptahydrate
Target:  

Antifolate Autophagy

Forschungsgebiete:  

Cancer

Pemetrexed disodium heptahydrate is a novel antifolate, the Ki values of the pentaglutamate of LY231514 are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively.
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40
40 Cited Publications
Art. -Nr.: HY-10820
CAS. Nr.: 137281-23-3
Reinheit:  99.91%
Synonyms: LY231514
Target:  

Antifolate Autophagy

Forschungsgebiete:  

Cancer

Pemetrexed (LY231514) is an antifolate, the Ki values of the pentaglutamate of Pemetrexed (LY231514) are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively .
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40
40 Cited Publications
Art. -Nr.: HY-10820A
CAS. Nr.: 150399-23-8
Reinheit:  99.79%
Synonyms: LY231514 disodium
Forschungsgebiete:  

Cancer

Pemetrexed disodium (LY231514 disodium) is an antifolate, the Kis of the pentaglutamate of Pemetrexed disodium are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively .
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40
40 Cited Publications
Art. -Nr.: HY-13781
CAS. Nr.: 357166-30-4
Reinheit:  99.78%
Synonyms: LY231514 disodium hemipenta hydrate
Pemetrexed (LY231514) disodium hemipenta hydrate is a CNS-penetrant antifolate, the Ki values of the pentaglutamate of LY231514 are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively.
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39
39 Cited Publications
Art. -Nr.: HY-10230
CAS. Nr.: 120685-11-2
Reinheit:  99.91%
Synonyms: PKC412; CGP 41251
Forschungsgebiete:  

Cancer

Midostaurin (PKC412; CGP 41251) is an orally active, reversible multi-targeted protein kinase inhibitor. Midostaurin inhibits PKCα/β/γ, Syk, Flk-1, Akt, PKA, c-Kit, c-Fgr, c-Src, FLT3, PDFRβ and VEGFR1/2 with IC50s ranging from 22-500 nM . Midostaurin also upregulates endothelial nitric oxide synthase (eNOS) gene expression. Midostaurin shows powerful anticancer effects .
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34
34 Cited Publications
Art. -Nr.: HY-B0218
CAS. Nr.: 96829-58-2
Synonyms: Tetrahydrolipstatin; Ro-18-0647
Forschungsgebiete:  

Metabolic Disease Cancer

Orlistat (Tetrahydrolipstatin) is a well-known irreversible inhibitor of pancreatic and gastric lipases. Orlistat is also an inhibitor of fatty acid synthase (FASN), is used orally for long-term research of obesity . Anti-atherosclerotic effect .
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30
30 Cited Publications
Art. -Nr.: HY-B1359
CAS. Nr.: 7220-79-3
Synonyms: C.I. Basic Blue 9 trihydrate
Methylene blue trihydrate (C.I. Basic Blue 9 trihydrate) is a guanylyl cyclase (sGC), monoamine oxidase A (MAO-A) and NO synthase (NOS) inhibitor. Methylene blue trihydrate is a vasopressor and is often used as a dye in several medical procedures. Methylene blue trihydrate has antinociception, antimalarial, antidepressant and anxiolytic activity effects. Methylene Blue trihydrate has the potential for methemoglobinemias, neurodegenerative disorders and ifosfamide-induced encephalopathytreatment .
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30
30 Cited Publications
Art. -Nr.: HY-14536
CAS. Nr.: 61-73-4
Reinheit:  95.05%
Synonyms: Basic Blue 9; CI-52015; Methylthioninium chloride
Methylene blue (Basic Blue 9) is a guanylyl cyclase (sGC), monoamine oxidase A (MAO-A) and NO synthase (NOS) inhibitor. Methylene blue is a vasopressor and is often used as a dye in several medical procedures. Methylene blue through the nitric oxide syntase/guanylate cyclase signalling pathway to reduce prepulse inhibition. Methylene blue is a REDOX cycling compound and able to cross the blood-brain barrier. Methylene blue is a Tau aggregation inhibitor. Methylene Blue is a photosensitizer and redox agent. Methylene blue reduces cerebral edema, attenuated microglial activation and reduced neuroinflammation .
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29
29 Cited Publications
Art. -Nr.: HY-18730
CAS. Nr.: 180001-34-7
Synonyms: W1400
1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a Kd value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .
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29
29 Cited Publications
Art. -Nr.: HY-18731
CAS. Nr.: 214358-33-5
1400W dihydrochloride is the dihydrochloride form of 1400W (HY-18730). 1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a Kd value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .
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27
27 Cited Publications
Art. -Nr.: HY-103087
CAS. Nr.: 1083162-61-1
Reinheit:  98.03%
Target:  

Ferroptosis

Forschungsgebiete:  

Others

FIN56 is a specific inducer of ferroptosis. FIN56 induces ferroptosis by inducing degradation of GPX4. FIN56 also binds to and activates squalene synthase .
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27
27 Cited Publications
Art. -Nr.: HY-D0958
CAS. Nr.: 122965-43-9
Synonyms: Basic Blue 9 hydrate; CI-52015 hydrate; Methylthioninium chloride hydrate
Methylene blue (Basic Blue 9) hydrate is a guanylyl cyclase (sGC), monoamine oxidase A (MAO-A) and NO synthase (NOS) inhibitor. Methylene blue is a vasopressor and is often used as a dye in several medical procedures. Methylene blue hydrate through the nitric oxide syntase/guanylate cyclase signalling pathway to reduce prepulse inhibition. Methylene blue hydrate is a REDOX cycling compound and able to cross the blood-brain barrier. Methylene blue hydrate is a Tau aggregation inhibitor. Methylene blue hydrate reduces cerebral edema, attenuated microglial activation and reduced neuroinflammation .
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25
25 Cited Publications
Art. -Nr.: HY-N0455
CAS. Nr.: 74-79-3
L-Arginine ((S)-(+)-Arginine) is the substrate for the endothelial nitric oxide synthase (eNOS) to generate NO. L-Arginine is transported into vascular smooth muscle cells by the cationic amino acid transporter family of proteins where it is metabolized to nitric oxide (NO), polyamines, or L-proline. L-Arginine is a potent vasodilator, and can be used to induce experimental acute pancreatitis .
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25
25 Cited Publications
Art. -Nr.: HY-N0455A
CAS. Nr.: 1119-34-2
Synonyms: (S)-(+)-Arginine hydrochloride
L-Arginine ((S)-(+)-Arginine) is the substrate for the endothelial nitric oxide synthase (eNOS) to generate NO. L-Arginine is transported into vascular smooth muscle cells by the cationic amino acid transporter family of proteins where it is metabolized to nitric oxide (NO), polyamines, or L-proline. L-Arginine is a potent vasodilator, and can be used to induce experimental acute pancreatitis .
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22
22 Cited Publications
Art. -Nr.: HY-16294
CAS. Nr.: 603288-22-8
Target:  

GSK-3

Forschungsgebiete:  

Cancer

LY2090314 is a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 values of 1.5 nM and 0.9 nM for GSK-3α and GSK-3β, respectively.
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