Metabolismo

Los inhibidores del metabolismo son compuestos que interfieren con las vías metabólicas, alterando la producción y utilización de energía dentro de las células. Estos inhibidores se utilizan para estudiar la regulación del metabolismo, el papel de las vías metabólicas en enfermedades como el cáncer y la diabetes, y para desarrollar nuevas estrategias terapéuticas. Los inhibidores del metabolismo pueden dirigirse a diversas enzimas y procesos involucrados en la glucólisis, la oxidación de ácidos grasos y otras funciones metabólicas. En CymitQuimica, ofrecemos una amplia gama de inhibidores del metabolismo de alta calidad para apoyar su investigación en bioquímica, trastornos metabólicos y desarrollo de fármacos.

Subcategorías de "Metabolismo"

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Se han encontrado 9275 productos de "Metabolismo"

Pureza (%)

100

productos por página.

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Imazodan
CAS:
- 84243-58-3
Imazodan is a compound with positive inotropic activity and is a type III phosphodiesterase inhibitor that can be used to study heart failure.
Fórmula:C₁₃H₁₂N₄O
Pureza:98% - 98.31%
Forma y color:Solid
Peso molecular:240.26
Ref: TM-T71744
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HSL-IN-1
CAS:
- 2095156-13-9
HSL-IN-1 is an HSL inhibitor that significantly reduces the reactive metabolite load and reduces the release of free fatty acids from stored fat.
Fórmula:C₁₉H₁₃BClF₃N₂O₄
Pureza:>99.99%
Forma y color:Solid
Peso molecular:436.58
Ref: TM-T11576
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Manitimus
CAS:
- 202057-76-9
Manitimus is a potent immunosuppressive drug, and is an inhibitor of dehydroorotate dehydrogenase,.
Fórmula:C₁₅H₁₁F₃N₂O₂
Pureza:99.75% - 99.75%
Forma y color:Solid
Peso molecular:308.26
Ref: TM-T11941
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FASN-IN-5
CAS:
- 1309805-49-9
FASN-IN-5 is a FASN inhibitor, useful for studying cancer and metabolic diseases.
Fórmula:C₂₉H₂₆N₄O₂
Pureza:99.88%
Forma y color:Solid
Peso molecular:462.54
Ref: TM-T62925
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MRL-871
CAS:
- 1392809-08-3
MRL-871 is a selective RORγt allosteric inhibitor, reducing IL-17a mRNA production in EL4 cells, interacting with PPARgamma in partial agonistic binding modes.
Fórmula:C₂₂H₁₂ClF₃N₂O₃
Pureza:99.66%
Forma y color:Solid
Peso molecular:444.79
Ref: TM-T62622
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Transketolase-IN-4
CAS:
- 419547-73-2
Transketolase-IN-4: IC50 3.9 μM; targets M. tuberculosis DXS (IC50 114.1 μM) & hinders SW620, LS174T, MIA PaCa-2 tumor cell growth.
Fórmula:C₁₉H₁₄ClN₃O
Pureza:99.52%
Forma y color:Solid
Peso molecular:335.79
Ref: TM-T72576
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ML218
CAS:
- 1346233-68-8
ML218 is an inhibitor of T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3).ML218 inhibits the synaptic activity of subthalamic nucleus (STN) neurons.
Fórmula:C₁₉H₂₆Cl₂N₂O
Pureza:99.2% - 99.45%
Forma y color:Solid
Peso molecular:369.33
Ref: TM-T12076L
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Piritrexim
CAS:
- 72732-56-0
Piritrexim (BW 301U) is an orally available fat-soluble dihydrofolate reductase inhibitor with pulmonary toxicity used in the study of uroepithelial carcinoma
Fórmula:C₁₇H₁₉N₅O₂
Pureza:98.50% - >99.99%
Forma y color:Solid
Peso molecular:325.37
Ref: TM-T24644
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PTP1B-IN-4
CAS:
- 765317-72-4
<p>PTP1B-IN-4 (NUN-17724) is an allosteric PTP1B inhibitor with an IC50 of 8 μM. PTP1B-IN-4 can be used in studies about obesity and diabetes.</p>
Fórmula:C₂₆H₁₉Br₂N₃O₇S₃
Pureza:98.19%
Forma y color:Solid
Peso molecular:741.45
Ref: TM-T24073
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MB05032
CAS:
- 261365-11-1
MB05032 is a fructose-,-bisphosphatase inhibitor that inhibits gluconeogenesis and may reduce d-lactate-triggered ETosis.
Fórmula:C₁₁H₁₅N₂O₄PS
Pureza:99.66%
Forma y color:Solid
Peso molecular:302.29
Ref: TM-T16020
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N-Acetylserine
CAS:
- 16354-58-8
N-Acetylserine (N-Acetyl-L-serine) serves as the physiological inducer of cysteine biosynthesis by binding to the CysB apoprotein and stimulating cysJIH
Fórmula:C₅H₉NO₄
Pureza:99.28%
Forma y color:Solid
Peso molecular:147.13
Ref: TM-T78617
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YZ9
CAS:
- 6093-71-6
Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 µM, and acts as a competitive inhibitor against Fru-6-P with a Ki of 0.094 µM[1].
Fórmula:C₁₂H₁₀O₅
Pureza:99.59%
Forma y color:Solid
Peso molecular:234.2
Ref: TM-T23552
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PD0176078
CAS:
- 248922-46-5
PD0176078 () is a newly blocker of N-type Calcium channel.
Fórmula:C₂₃H₃₀F₂N₂O
Pureza:99.72%
Forma y color:Solid
Peso molecular:388.49
Ref: TM-T12385
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CDC25B-IN-1
CAS:
- 2374831-10-2
<p>CDC25B-IN-1 is an inhibitor of CDC25B with a Ki of 8.5 μM. CDC25B-IN-1 increases the G2/M phase by inhibiting cell proliferation and colony formation.</p>
Fórmula:C₂₀H₁₉NO₃
Pureza:97.05%
Forma y color:Solid
Peso molecular:321.37
Ref: TM-T10723
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(R)-Lercanidipine hydrochloride
CAS:
- 187731-34-6
(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a blocker of calcium channel.
Fórmula:C₃₆H₄₂ClN₃O₆
Pureza:98%
Forma y color:Solid
Peso molecular:648.2
Ref: TM-T12626
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NF-1819
CAS:
- 1881244-28-5
NF-1819: strong, selective MGL inhibitor; eases MS symptoms; analgesic; penetrates brain with high permeability.
Fórmula:C₂₄H₂₂FN₅O₄
Pureza:99.55%
Forma y color:Solid
Peso molecular:463.46
Ref: TM-T28165
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AZD8329
CAS:
- 1048668-70-7
AZD8329 is an 11β-HSD1 inhibitor that inhibits 11β-HSD2, 17β-HSD1, 17β-HSD3, and can be used to study allergic reactions in humans.
Fórmula:C₂₅H₃₁N₃O₃
Pureza:99.31%
Forma y color:Solid
Peso molecular:421.53
Ref: TM-T14383
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Brofaromine
CAS:
- 63638-91-5
Brofaromine (CGP 11305A) is an MAO inhibitor (IC50: 0.2 μM for MAO-A).
Fórmula:C₁₄H₁₆BrNO₂
Forma y color:Solid
Peso molecular:310.19
Ref: TM-T10617
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2-Hydroxy atorvastatin calcium salt
CAS:
- 265989-46-6
2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt which is a potent HMG-CoA reductase inhibitor (IC50 = 8 nM).
Fórmula:C₆₆H₆₈CaF₂N₄O₁₂
Pureza:97.06% - 99.92%
Forma y color:Solid
Peso molecular:1187.36
Ref: TM-TQ0045
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PGMI-004A
CAS:
- 1313738-90-7
PGMI-004A is an effective inhibitor of phosphoglycerate mutase 1 (IC50: 13.1 μM).
Fórmula:C₂₁H₁₂F₃NO₆S
Pureza:98%
Forma y color:Solid
Peso molecular:463.38
Ref: TM-T16517