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 8595 productos de "Metabolismo"

Pureza (%)

100

productos por página.

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G6PD activator AG1
CAS:
- 421581-52-4
G6PD activator AG1 is a G6PD agonist that promotes G6PD oligomerization to a catalytically competent form.
Fórmula:C₂₄H₃₀N₄S₂
Pureza:98.38% - 99.51%
Forma y color:Solid
Peso molecular:438.65
Ref: TM-T11347
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CX-157
CAS:
- 205187-53-7
CX-157 (KP 157) is a novel monoamine oxidase-A (MAO-A) inhibitor for the study of depression-like neurological disorders and cancer.
Fórmula:C₁₄H₈F₄O₄S
Pureza:99.35%
Forma y color:Solid
Peso molecular:348.27
Ref: TM-T15023
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K-111
CAS:
- 221564-97-2
K-111 is a PPAR alpha agonist. K-111 improves insulin resistance, reducing bodyweight, and ameliorating atherogenic dyslipidemia.
Fórmula:C₁₈H₂₅Cl₃O₂
Pureza:99.64% - 99.88%
Forma y color:Solid
Peso molecular:379.75
Ref: TM-T27706
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L-Threonine derivative-1
CAS:
- 852055-88-0
L-Threonine derivative-1 is acetylsalicylic acid-L-threonine ester with potential analgesic activity.
Fórmula:C₁₃H₁₅NO₆
Pureza:97.03% - 98.91%
Forma y color:Solid
Peso molecular:281.26
Ref: TM-T13751
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HSD-016
CAS:
- 946396-92-5
HSD-016: Oral 11β-HSD1 inhibitor, active in humans, mice, rats (IC50: 11, 1, 8 nM), potential for type 2 diabetes research.
Fórmula:C₂₁H₂₁F₇N₂O₃S
Pureza:99.40% - >99.99%
Forma y color:Solid
Peso molecular:514.46
Ref: TM-T63569
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AC-261066
CAS:
- 870773-76-5
AC-261066 is an orally available and isoform-selective agonist of RARβ2 with a pEC50 of 8.0.
Fórmula:C₁₇H₂₀FNO₄S
Pureza:99.64%
Forma y color:Solid
Peso molecular:353.41
Ref: TM-T14089
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S-2474
CAS:
- 158089-95-3
S-2474, an inhibitor of COX-2 and 5-lipoxygenase, has anti-inflammatory and neuroprotective activities, and inhibits cell death.
Fórmula:C₂₀H₃₁NO₃S
Pureza:99.03%
Forma y color:Solid
Peso molecular:365.53
Ref: TM-T16817
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AM 374
CAS:
- 86855-26-7
AM 374 (HDSF), a fatty acid amide hydrolase (FAAH) inhibitor, demonstrates the capacity to inhibit amidase activity, boasting an IC50 value of 13 nM.
Fórmula:C₁₆H₃₃FO₂S
Pureza:98.39%
Forma y color:Solid
Peso molecular:308.5
Ref: TM-T68492
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Carbazeran
CAS:
- 70724-25-3
Carbazeran (UK-31,557) is an inhibitor of PDE2 and PDE3 and can be used for studies about metabolic diseases.
Fórmula:C₁₈H₂₄N₄O₄
Pureza:99.3%
Forma y color:Solid
Peso molecular:360.41
Ref: TM-T21457
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CYP1B1-IN-5
CAS:
- 176442-56-1
CYP1B1-IN-5: selective CYP1B1 inhibitor, IC50 = 4.7 nM, useful for metabolism disease research.
Fórmula:C₁₄H₈INO₂
Pureza:98.61%
Forma y color:Solid
Peso molecular:349.12
Ref: TM-T73042
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OSMI-4
CAS:
- 2260791-14-6
OSMI-4 is a low nanomolar O-GlcNAc transferase (OGT) inhibitor that can be used to study OGT inhibition in different human cell lines.Cost-effective and quality-assured.
Fórmula:C₂₇H₂₆ClN₃O₇S₂
Pureza:99.68%
Forma y color:Solid
Peso molecular:604.09
Ref: TM-T12328
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BMS-823778
CAS:
- 1140897-32-0
BMS-823778 is a potent inhibitor of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) for the study of type 2 diabetes.
Fórmula:C₁₈H₁₈ClN₃O
Pureza:99.39% - 99.75%
Forma y color:Solid
Peso molecular:327.81
Ref: TM-T71394
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Ch55
CAS:
- 110368-33-7
Ch55, a potent HL60 cell differentiator (EC50=200nM), binds well to RAR-α/β, useful for cancer research.
Fórmula:C₂₄H₂₈O₃
Pureza:99.55%
Forma y color:Solid
Peso molecular:364.48
Ref: TM-T14946
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Crobenetine
CAS:
- 221019-25-6
Crobenetine (BIII 890 CL) Free Base is a selective NaV channel blocker that eliminates VTD-induced [Ca2+] elevation.
Fórmula:C₂₅H₃₃NO₂
Pureza:98.99%
Forma y color:Solid
Peso molecular:379.54
Ref: TM-T69795
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YM 511
CAS:
- 148869-05-0
YM 511 is a specific non-steroidal aromatase inhibitor with IC50s of 0.4 and 0.12 nM, minimally affecting other steroids.
Fórmula:C₁₆H₁₂BrN₅
Pureza:99.965%
Forma y color:Solid
Peso molecular:354.2
Ref: TM-T23549
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Dovramilast
CAS:
- 340019-69-4
Dovramilast (CC-11050) is a PDE4 inhibitor that reduces the production of pro-inflammatory mediators in lupus erythematosus.
Fórmula:C₂₄H₂₈N₂O₆S
Pureza:98.75% - 99.62%
Forma y color:Solid
Peso molecular:472.55
Ref: TM-T63056
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Fumarate hydratase-IN-1
CAS:
- 1644060-37-6
Fumarate hydratase-IN-1 is a cell-permeable fumarate hydratase inhibitor with antiproliferative activity and can be used to study cellular activity.
Fórmula:C₂₇H₃₀N₂O₄
Pureza:98.96% - 99.49%
Forma y color:Solid
Peso molecular:446.54
Ref: TM-T11337
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IQB-782
CAS:
- 40454-21-5
IQB-782 is a mucolytic agent with mucolytic expectorant activity for the study of obstructive lung disease.
Fórmula:C₄H₉N₃O₂S
Pureza:>99.99%
Forma y color:Solid
Peso molecular:163.2
Ref: TM-T11668
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AICAR monophosphate
CAS:
- 3031-94-5
AICAR monophosphate (Aica ribonucleotide) is a purine precursor with antineoplastic activity and can be used in studies about type 2 diabetes.
Fórmula:C₉H₁₅N₄O₈P
Pureza:99.8%
Forma y color:Solid
Peso molecular:338.21
Ref: TM-T21195
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KRH102140
CAS:
- 864769-01-7
KRH102140 is a PHD2 activator that reduces angiogenesis by inhibiting HIF-1alpha, used in cardiovascular disease research.
Fórmula:C₂₅H₂₄FNO
Pureza:98.31% - 99.61%
Forma y color:Solid
Peso molecular:373.46
Ref: TM-T68511