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 8626 productos de "Metabolismo"

Pureza (%)

100

productos por página.

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KCA-1490
CAS:
- 909719-71-7
KCA-1490 is an inhibitor of dual PDE3/4.
Fórmula:C₁₄H₁₃F₃N₄O₂
Pureza:98%
Forma y color:Solid
Peso molecular:326.27
Ref: TM-T24257
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BMS-185411
CAS:
- 166977-24-8
BMS-185411 is a bio-active chemical.
Fórmula:C₂₆H₂₃NO₃
Forma y color:Solid
Peso molecular:397.47
Ref: TM-T30497
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SHP394
CAS:
- 2055757-40-7
SHP394 is an orally efficacious inhibitor of protein tyrosine phosphatase SHP2 (IC50: 23 nM).
Fórmula:C₂₀H₂₅F₃N₆O₂S
Pureza:98%
Forma y color:Solid
Peso molecular:470.51
Ref: TM-T16877
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sEH/AChE-IN-3
CAS:
- 2490589-11-0
sEH/AChE-IN-3 -15: potent dual sEH & AChE inhibitor; crosses BBB; IC50: hsEH 0.4nM, hAChE 1.94nM, hBChE 615nM, msEH 4.3nM, mAChE 2.61nM.
Fórmula:C₃₅H₃₉ClF₃N₅O₃
Forma y color:Solid
Peso molecular:670.16
Ref: TM-T72875
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hCAIX-IN-15
CAS:
- 2849348-43-0
hCAIX-IN-15 is a potent inhibitor of human carbonic anhydrase IX (hCA IX) with an inhibition constant (Ki) of 38.8 nM, exhibiting broad-spectrum anticancer
Fórmula:C₁₈H₁₄FN₇O₂S
Pureza:98%
Forma y color:Solid
Peso molecular:411.41
Ref: TM-T73029
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α-Glucosidase-IN-28
CAS:
- 2949513-10-2
α-Glucosidase-IN-28 (Compound 18) is an α-glucosidase inhibitor with an IC50 of 0.62 μM and Ki value of 3.93 μM.
Fórmula:C₂₉H₂₂Br₂O₇
Pureza:98%
Forma y color:Solid
Peso molecular:642.29
Ref: TM-T78740
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ICMT-IN-19
CAS:
- 1313603-00-7
ICMT-IN-19 (compound 53) serves as a potent inhibitor of ICMT, demonstrating an IC50 value of 0.026 μM [1].
Fórmula:C₂₁H₂₆N₂O₃
Forma y color:Solid
Peso molecular:354.44
Ref: TM-T82126
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hCAIX/XII-IN-8
CAS:
- 59994-64-8
hCAIX/XII-IN-8 (compound 3g) is a potent inhibitor of the human carbonic anhydrases (CAs) IX and XII, with inhibition constants (K i) of 8.5 nM for CA IX and 6.
Fórmula:C₁₆H₁₃Cl₂N₅O₃S
Pureza:98%
Forma y color:Solid
Peso molecular:426.28
Ref: TM-T79753
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UCPH-102
CAS:
- 1229591-56-3
UCPH-102: Selective EAAT1 inhibitor, IC50 0.43 μM, treats Alzheimer's, ALS, chronic pain, OCD; crosses blood-brain barrier, targets T-ALL cells.
Fórmula:C₂₁H₁₈N₂O₂
Forma y color:Solid
Peso molecular:330.38
Ref: TM-T60966
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Cav 3.2 inhibitor 4
CAS:
- 1416984-93-4
Cav 3.2 Inhibitor 4 (Compound 21) is a selective and potent inhibitor of the T-type calcium channel (Ca v 3.2), demonstrating peripheral restriction with an
Fórmula:C₂₁H₃₂Cl₂N₄O₃
Pureza:98%
Forma y color:Solid
Peso molecular:459.41
Ref: TM-T79195
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Phenylpyropene C
CAS:
- 419532-92-6
Phenylpyropene C inhibits JAK/STAT and IFN-γ expression (IC50: 5.4-10.8 μM), also blocks acyl CoA (IC50: 16.0 μM).
Fórmula:C₂₈H₃₄O₅
Forma y color:Solid
Peso molecular:450.57
Ref: TM-T62726
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ICMT-IN-36
CAS:
- 1313602-86-6
ICMT-IN-36 (compound 40) serves as an ICMT inhibitor, with an IC50 value of 0.181 μM [1].
Fórmula:C₂₁H₂₅Cl₂NO
Forma y color:Solid
Peso molecular:378.34
Ref: TM-T82107
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BBT
CAS:
- 445000-45-3
BBT has anti-hyperglycemic activity, protecting beta cells from cytokine or streptozotocin-induced cell death, and restoring beta cell function.
Fórmula:C₁₈H₁₂BrNO₂S
Pureza:99.02%
Forma y color:Solid
Peso molecular:386.26
Ref: TM-T78066
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ERX-41
CAS:
- 2440087-54-5
ERX-41 is an orally active, stereospecific small molecule that targets lysosomal acid lipase A (LIPA).
Fórmula:C₃₈H₄₈N₄O₉
Pureza:98%
Forma y color:Solid
Peso molecular:704.81
Ref: TM-T78528
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BAY-7081
BAY-7081 is a cyanopyridone-based compound that functions as a potent, selective, and orally active PDE9A inhibitor, demonstrating an inhibition concentration (
Fórmula:C₁₉H₂₇ClN₄O
Forma y color:Solid
Peso molecular:362.9
Ref: TM-T73394
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H-0106 Dihydrochloride
CAS:
- 1011465-90-9
H-0106 Dihydrochloride is an inhibitor of ROCK that acts by applying strong intraocular pressure (IOP)-lowering effects into the eyes of monkeys.
Fórmula:C₁₆H₂₂Cl₃N₃O₂S
Pureza:98%
Forma y color:Solid
Peso molecular:426.79
Ref: TM-T25483
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VT-1598 tosylate
CAS:
- 2089321-00-4
VT-1598 tosylate is a selective, orally active antifungal compound that targets CYP51. It demonstrates efficacy against C. auris.
Fórmula:C₃₈H₂₈F₄N₆O₅S
Forma y color:Solid
Peso molecular:756.72
Ref: TM-T72660
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PF-04937319
CAS:
- 1245603-92-2
PF-04937319 activates glucokinase (EC50=154.4μM) with low hypoglycemia risk, researched for type 2 diabetes treatment.
Fórmula:C₂₂H₂₀N₆O₄
Pureza:99.89%
Forma y color:Solid
Peso molecular:432.43
Ref: TM-T16479
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Diethyl-pythiDC
CAS:
- 1821370-70-0
Diethyl-pythiDC is an collagen prolyl 4-hydroxylase inhibitor.
Fórmula:C₁₄H₁₄N₂O₄S
Pureza:99.98%
Forma y color:Solid
Peso molecular:306.34
Ref: TM-T15124
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GPX4-IN-2
CAS:
- 2485005-22-7
GPX4-IN-2 is a potent inhibitor of GPX4, exhibiting antiproliferative activity. It holds potential for cancer research applications.
Fórmula:C₃₀H₄₀N₂O
Forma y color:Solid
Peso molecular:444.65
Ref: TM-T73235