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 8597 productos de "Metabolismo"

Pureza (%)

100

productos por página.

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BMS 753
CAS:
- 215307-86-1
BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).
Fórmula:C₂₁H₂₁NO₄
Pureza:98.55%
Forma y color:Solid
Peso molecular:351.4
Ref: TM-T22049
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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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PC945
CAS:
- 1931946-73-4
PC945 (Opelconazole) is an antifungal compound that inhibits CYP51A/CYP51B and can be used to study fungal infections of the lungs.
Fórmula:C₃₈H₃₇F₃N₆O₃
Pureza:98.89% - 99.37%
Forma y color:Solid
Peso molecular:682.73
Ref: TM-T12376
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SBI-425
CAS:
- 1451272-71-1
SBI-425: orally available TNAP inhibitor, enhances cardiovascular health & survival, no bone impact.
Fórmula:C₁₃H₁₂ClN₃O₄S
Pureza:99.88%
Forma y color:Solid
Peso molecular:341.77
Ref: TM-T16859
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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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MAO-B-IN-8
CAS:
- 1638956-60-1
MAO-B-IN-8 is a highly potent and reversible inhibitor of monoamine oxidase-B (MAO-B), which also exhibits inhibitory effects on the microglial production of
Fórmula:C₁₈H₁₆O₆
Pureza:99.62%
Forma y color:Solid
Peso molecular:328.32
Ref: TM-T60932
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Vatanidipine
CAS:
- 116308-55-5
Vatanidipine (AE0047) is a novel dihydropyridine (DHP)-type calcium channel blocker with slow-onset pharmacological actions.A slow-onset and long-lasting
Fórmula:C₄₁H₄₂N₄O₆
Pureza:99.95%
Forma y color:Solid
Peso molecular:686.8
Ref: TM-T24932
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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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JJKK 048
CAS:
- 1515855-97-6
JJKK 048 is a potent and selective MAGL inhibitor.
Fórmula:C₂₃H₂₂N₄O₅
Pureza:99.77%
Forma y color:Solid
Peso molecular:434.44
Ref: TM-T15614
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Malic enzyme inhibitor ME1
CAS:
- 522649-59-8
Malic enzyme inhibitor ME1 (ME1) is a specific inhibitor of Malic enzyme (IC50 = 0.15 μM). Malic enzyme inhibitor ME1 reduces cell viability/metabolic activity.
Fórmula:C₂₀H₂₁N₃O₃
Pureza:99.84%
Forma y color:Solid
Peso molecular:351.4
Ref: TM-T11940
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Sultiame
CAS:
- 61-56-3
Sultiame is an inhibitor of carbonic anhydrase. Sultiame can be used in antiepileptic research.
Fórmula:C₁₀H₁₄N₂O₄S₂
Pureza:99.91%
Forma y color:Solid
Peso molecular:290.36
Ref: TM-T16960
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5-LOX-IN-1
CAS:
- 55040-82-9
5-LOX-IN-1 is a 5-Lipoxygenase (5-LOX) inhibitor (IC50: 2.3 μM).5-LOX-IN-1 can be used for cancer research.
Fórmula:C₂₀H₁₈N₂O₂S
Pureza:97.45%
Forma y color:Solid
Peso molecular:350.43
Ref: TM-T61211
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BW-1370U87
CAS:
- 134476-36-1
BW-1370U87 is an MAO-A inhibitor increasing brain amines, showing promise in depression models.
Fórmula:C₁₄H₁₂O₃S
Pureza:99.82% - 99.89%
Forma y color:Solid
Peso molecular:260.31
Ref: TM-T26930
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Imanixil
CAS:
- 75689-93-9
Imanixil boosts LDLR, cuts cholesterol and VLDL production, reducing atherosclerosis.
Fórmula:C₁₇H₁₇F₃N₆O₂
Pureza:>99.99% - >99.99%
Forma y color:Solid
Peso molecular:394.35
Ref: TM-T15561
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AWD 12-281
CAS:
- 257892-33-4
AWD 12-281 is a PDE4 inhibitor with anti-inflammatory activity and bronchodilator activity for the study of chronic obstructive pulmonary disease (COPD).
Fórmula:C₂₂H₁₄Cl₂FN₃O₃
Pureza:99.25% - 99.85%
Forma y color:Solid
Peso molecular:458.27
Ref: TM-T30232
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Indeglitazar
CAS:
- 835619-41-5
Indeglitazar (PPM 204) is orally available pan-agonist of PPAR (PPAR subtypes alpha (α), delta (δ), and gamma (γ)).
Fórmula:C₁₉H₁₉NO₆S
Pureza:99.45%
Forma y color:Solid
Peso molecular:389.42
Ref: TM-T15575
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11-cis-Vaccenyl acetate
CAS:
- 6186-98-7
11-cis-Vaccenyl acetate ((Z)-Octadec-11-enyl acetate) activates olfactory neurons located in the T1 sensilla on the antenna and mediates aggregation behavior in
Fórmula:C₂₀H₃₈O₂
Pureza:96.53% - 99.95%
Forma y color:Liquid
Peso molecular:310.51
Ref: TM-T10038
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Rbin-2
CAS:
- 2032282-97-4
Rbin-2: Potent, selective Midasin inhibitor; reversible, cell-permeable; halts eukaryotic ribosome assembly.
Fórmula:C₁₃H₁₁BrN₄S
Pureza:98.75%
Forma y color:Solid
Peso molecular:335.22
Ref: TM-T28506
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PD173212
CAS:
- 217171-01-2
PD 173212 is a blocker that blocks N-type voltage sensitive calcium channel (Cav2.2).
Fórmula:C₃₈H₅₃N₃O₃
Pureza:99.84%
Forma y color:Solid
Peso molecular:599.85
Ref: TM-T16448
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GSK205
CAS:
- 1263068-83-2
GSK205 is a selective TRPV4 antagonist (IC50: 4.19 μM) for inhibiting TRPV4-mediated Ca2+ influx.
Fórmula:C₂₄H₂₅BrN₄S
Pureza:99.46%
Forma y color:Solid
Peso molecular:481.45
Ref: TM-T11480