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 8625 productos de "Metabolismo"

Pureza (%)

100

productos por página.

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Xanthine oxidase-IN-1
CAS:
- 1071970-13-2
Xanthine oxidase-IN-1 is an effective inhibitor of xanthine oxidase with an IC50 value of 6.5 nM.
Fórmula:C₁₆H₈F₂N₂O₃
Pureza:97.36% - 99.22%
Forma y color:Solid
Peso molecular:314.24
Ref: TM-T10509
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OGT 2115
CAS:
- 853929-59-6
OGT 2115 blocks heparanase (IC50=0.4µM), cleaving heparan sulfate; antiangiogenic (IC50=1µM).
Fórmula:C₂₄H₁₆BrFN₂O₄
Pureza:97.17%
Forma y color:Solid
Peso molecular:495.3
Ref: TM-T16380
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Dechloro Rivaroxaban
CAS:
- 1415566-28-7
Dechloro Rivaroxaban is a Factor Xa inhibitor that inhibits free FXa and plasminogen and fibrin-associated FXa activity in humans.
Fórmula:C₁₉H₁₉N₃O₅S
Pureza:98.63%
Forma y color:Solid
Peso molecular:401.44
Ref: TM-T78215
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WAY-620147
CAS:
- 515866-67-8
WAY-620147 inhibits Monoamine Oxidase and can be used for the study of neurological disorders.
Fórmula:C₁₂H₁₆BrN₃O₂
Pureza:99.55%
Forma y color:Solid
Peso molecular:314.18
Ref: TM-T80799
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PDE9-IN-(S)-C33
CAS:
- 2066488-39-7
PDE9-IN-(S)-C33: potent PDE9 inhibitor with 11 nM IC50, for CNS diseases and diabetes study.
Fórmula:C₁₈H₂₀ClN₅O
Pureza:98.75%
Forma y color:Solid
Peso molecular:357.84
Ref: TM-T28352
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TP-10
CAS:
- 898563-00-3
TP-10 is a selective inhibitor of PDE10A against other PDEs with IC50 of 0.8 nM.
Fórmula:C₂₆H₁₉F₃N₄O
Pureza:99.21%
Forma y color:Solid
Peso molecular:460.45
Ref: TM-T13189
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TPN171
CAS:
- 1229018-87-4
TPN171 is potent PDE5 inhibitor with subnanomolar potency for PDE5 and good selectivity over PDE6, which has the potential for the treatment of pulmonary
Fórmula:C₂₄H₃₅N₅O₃
Pureza:>99.99%
Forma y color:Solid
Peso molecular:441.57
Ref: TM-T13193
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Mutant IDH1-IN-2
CAS:
- 1429176-69-1
Mutant IDH1-IN-2 is a inhibitor of mutant Isocitrate dehydrogenase (IDH) proteins, with IC50 of 16.6 nM in Fluorescence biochemical assay, IC50 of ＜22 nM in LS-
Fórmula:C₂₄H₃₁F₂N₅O₂
Pureza:99.88%
Forma y color:Solid
Peso molecular:459.53
Ref: TM-T12128
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ALOX15-IN-1
ALOX15-IN-1 (8b) inhibits rabbit/human ALOX15; IC50: 0.04 μM for LA, 2.06 μM for AA.
Fórmula:C₂₄H₃₁N₃O₅S
Forma y color:Solid
Peso molecular:473.59
Ref: TM-T63075
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Nampt-IN-13
CAS:
- 2592504-89-5
Nampt-IN-13 (example 58m) is an NAMPT inhibitor used in the synthesis of antibody-drug conjugates (ADCs).
Fórmula:C₂₄H₃₀N₆O₂
Forma y color:Solid
Peso molecular:434.53
Ref: TM-T201106
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Keto lovastatin
CAS:
- 96497-73-3
Keto lovastatin is an impurity of lovastatin with antibacterial properties. Lovastatin is a cell-permeable HMG-CoA reductase (HMG-CoA reductase) inhibitor used to reduce cholesterol levels.
Fórmula:C₂₄H₃₄O₆
Forma y color:Solid
Peso molecular:418.523
Ref: TM-T204532
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Z21090
CAS:
- 2992690-71-6
Z21090 (ZL40) is a highly effective inhibitor of PDE 4, exhibiting an IC 50 value of 37.4 nM, and possesses oral bioavailability. It is significant in the study of alcohol-related diseases [1].
Fórmula:C₁₂H₁₄ClN₃O₃
Forma y color:Solid
Peso molecular:283.71
Ref: TM-T87655
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Enpp-1-IN-7
Enpp-1-IN-7: potent enpp-1 inhibitor, broad specificity, potential in cancer/infectious disease research. (WO2021203772A1)
Fórmula:C₁₈H₁₉N₇O₄S
Forma y color:Solid
Peso molecular:429.45
Ref: TM-T62368
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JA2
CAS:
- 277333-45-6
JA2 is an inhibitor of metalloendopeptidase 24.15 that enhances the hypotensive response to bradykinin in rats.
Fórmula:C₃₃H₃₈N₄O₈
Forma y color:Solid
Peso molecular:618.68
Ref: TM-T200905
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Asimicin
CAS:
- 102989-24-2
Asimicin is a effective complex I inhibitor.
Fórmula:C₃₇H₆₆O₇
Pureza:98%
Forma y color:Solid
Peso molecular:622.92
Ref: TM-T25115
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MAGL-IN-19
CAS:
- 2411570-42-6
MAGL-IN-19 (compound 7o) is a highly effective and selective inhibitor of MAGL.
Fórmula:C₂₁H₂₆F₃N₃O₃
Forma y color:Solid
Peso molecular:425.45
Ref: TM-T200603
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1,2-Dipentadecanoyl-rac-glycerol
CAS:
- 98896-79-8
1,2-Dipentadecanoyl-rac-glycerol (DG(15:0/15:0/0:0)) is a compound referenced in studies examining the effect of insulin on the content of 1,2-diacylglycerol in rat hearts. Insulin is observed to increase the amount of 1,2-diacylglycerol containing specific fatty acid compositions in the heart, which may be linked to cardiac contractility.
Fórmula:C₃₃H₆₄O₅
Forma y color:Solid
Peso molecular:540.86
Ref: TM-T200814
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RORγt inverse agonist 32
CAS:
- 2301159-96-4
RORγt inverse agonist 32 (compound b14) exhibits oral activity and can be utilized in inflammatory research studies.
Fórmula:C₂₄H₂₈F₃NO₅S
Forma y color:Solid
Peso molecular:499.54
Ref: TM-T200887
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MDL-100240
CAS:
- 142695-08-7
MDL-100240 inhibits ACE/neprilysin, effective against hypertension-induced heart/vascular changes.
Fórmula:C₂₆H₂₈N₂O₅S
Pureza:98%
Forma y color:Solid
Peso molecular:480.58
Ref: TM-T28005
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ABT-046
CAS:
- 1031336-60-3
ABT-046 is an orally active, selective, and highly efficient Diacylglycerol Acyltransferase 1 (DGAT-1) inhibitor that can be used in metabolic disease research.
Fórmula:C₂₀H₂₂N₄O₂
Pureza:98.13%
Forma y color:Solid
Peso molecular:350.41
Ref: TM-T14085