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Filtered Search Results
eMolecules 510758-28-8 | Tris(benzyltriazolylmethyl)amine | Ambeed | MFCD09265124 | 530.640 | C30H30N10 | 97.000 | C(N(Cc1cn(Cc2ccccc2)nn1)Cc1cn(Cc2ccccc2)nn1)c1cn(Cc2ccccc2)nn1 | 250mg | 516644589
Tris(benzyltriazolylmethyl)amine | Ambeed | 510758-28-8 | MFCD09265124 | 530.640 | C30H30N10 | 97.000 | C(N(Cc1cn(Cc2ccccc2)nn1)Cc1cn(Cc2ccccc2)nn1)c1cn(Cc2ccccc2)nn1 | 250mg | 516644589
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eMolecules 1374014-30-8 | 3-(Bromomethyl)oxetane | Ambeed | MFCD20278240 | 151.003 | C4H7BrO | 95.000 | BrCC1COC1 | 100mg | 525090553
3-(Bromomethyl)oxetane | Ambeed | 1374014-30-8 | MFCD20278240 | 151.003 | C4H7BrO | 95.000 | BrCC1COC1 | 100mg | 525090553
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Medchemexpress LLC 2'-O,4'-C-Methyleneadenosine | 206055-70-1 | 99.9% | 279.26 | 250 MG
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2'-O,4'-C-Methyleneadenosine (LNA-A) is a locked nucleic acid (LNA) and an adenosine analog. It is for research use only and not sold to patients. This product exhibits antiviral activity against wild type Hepatitis C virus genotype 1b in human HuH7 cells.
- Locked nucleic acid (LNA)
- Adenosine analog
- High purity (99.9%)
- Antiviral activity against wild type Hepatitis C virus genotype 1b in human HuH7 cells (EC50 > 50 μM)
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Medchemexpress LLC N-methyl paroxetine | 110429-36-2 | MFCD03788781 | 250mg
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N-Methylparoxetine is a derivative of Paroxetine that induces Apoptosis NSCLC cells by activating mitogen-activated protein kinase ( MAPK) N-Methylparoxetine has antitumor activity[1]
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![Medchemexpress LLC 3-azaspiro[5.5]undecane hydrochloride | 1125-01-5 | MFCD02093801 | 97.0% | 189.73 g·mol⁻¹ | C10H20ClN | 250 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000241179.png-250.jpg)
Medchemexpress LLC 3-azaspiro[5.5]undecane hydrochloride | 1125-01-5 | MFCD02093801 | 97.0% | 189.73 g·mol⁻¹ | C10H20ClN | 250 MG
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3-Azaspiro[5.5]undecane hydrochloride is a spirocyclic small molecule supplied as the hydrochloride salt for research use. It is a white to off-white solid with reported purity ≥97% and molecular weight 189.73 g·mol⁻¹. The compound has been reported to inhibit the wild-type influenza A virus M2 proton channel (A/M2) with an IC50 of 1 μM (two-electrode patch clamp assay).
- Inhibits influenza A virus M2 proton channel (IC50 1 μM).
- Supplied as a stable white to off-white solid.
- Chemical formula C10H20ClN and molecular weight 189.73 g·mol⁻¹.
- High reported purity (≥97%) suitable for research applications.
- Available in multiple laboratory pack sizes for flexibility.
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Medchemexpress LLC 3(2H)-Pyridazinone, 6-[4-[3-[(2R)-2-methyl-1-pyrrolidinyl]propoxy]phenyl]- | 1005402-19-6 | 99.6% | 313.39 | 250 MG
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3(2H)-Pyridazinone, 6-[4-[3-[(2R)-2-methyl-1-pyrrolidinyl]propoxy]phenyl]- | 1005402-19-6 | 99.6% | 313.39 | 250 MG
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![eMolecules 1599440-13-7 | Deruxtecan | Ambeed1034.068 | C52H56FN9O13 | 98.000 | CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc(F)c(C)c5CC[C@H](NC(=O)COCNC(=O)CNC(=O)[C@H](Cc6ccccc6)NC(=O)CNC(=O)CNC(=O)CCCCCN6C(=O)C=CC6=O)c(c3Cn1c2=O)c45 | 250mg | 811908443](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128234.jpg-250.jpg)
eMolecules 1599440-13-7 | Deruxtecan | Ambeed1034.068 | C52H56FN9O13 | 98.000 | CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc(F)c(C)c5CC[C@H](NC(=O)COCNC(=O)CNC(=O)[C@H](Cc6ccccc6)NC(=O)CNC(=O)CNC(=O)CCCCCN6C(=O)C=CC6=O)c(c3Cn1c2=O)c45 | 250mg | 811908443
Deruxtecan | Ambeed | 1599440-13-71034.068 | C52H56FN9O13 | 98.000 | CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cc(F)c(C)c5CC[C@H](NC(=O)COCNC(=O)CNC(=O)[C@H](Cc6ccccc6)NC(=O)CNC(=O)CNC(=O)CCCCCN6C(=O)C=CC6=O)c(c3Cn1c2=O)c45 | 250mg | 811908443
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Medchemexpress LLC Ethyl 2-chloroacetoacetate | 609-15-4 | MFCD00009141 | 99.6% | 164.59 g/mol | C6H9ClO3 | 1kg
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Ethyl 2-chloroacetoacetate (A 21960) is a Tn3 resolvase inhibitor and inhibit synapse formation between resolvase and two directly repeated res sites[1]
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Medchemexpress LLC Ethyl cinnamate | 103-36-6 | MFCD00009189 | 99.8% | 176.21 g/mol | C11H12O2 | 250g
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Ethyl cinnamate an orally active chemical constituent of the rhizome of Kaempferia galanga exhibits anti-cancer nematocidal sedative and vasorelaxant activities Ethyl cinnamate is a fragrance ingredient used as a food flavor and additive for cosmetic products Ethyl cinnamate is also an excellent clearing reagent for mammalian tissues Ethyl cinnamate suppresses tumor growth through anti-angiogenesis by attenuating VEGFR2 signal pathway in colorectal cancer Ethyl cinnamate inhibits the tonic contractions induced by high K and phenylephrine (PE) with respective IC50 values of 0 30 mM and 0 38 mM in rat aorta[1][2][3][4]
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Medchemexpress LLC Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride | 347890-34-0 | MFCD01862956 | 97.0% | 282.76 g/mol | C11H23ClN2O4 | 5g
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Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride is a Glycine (HY-Y0966) derivative[1]
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eMolecules 1215107-29-1 | Ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropanecarboxylate | Combi-Blocks | MFCD24449649 | 240.110 | C12H21BO4 | 95.000 | CCOC(=O)C1CC1B1OC(C)(C)C(C)(C)O1 | 25g | 439369561
Ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropanecarboxylate | Combi-Blocks | 1215107-29-1 | MFCD24449649 | 240.110 | C12H21BO4 | 95.000 | CCOC(=O)C1CC1B1OC(C)(C)C(C)(C)O1 | 25g | 439369561
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Medchemexpress LLC Ilaprazole sodium hydrate | 2322264-11-7 | 99.15% | 250 MG
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Ilaprazole (IY-81149) sodium hydrate is an orally active proton pump inhibitor. It irreversibly inhibits H+/K+-ATPase in a dose-dependent manner with an IC50 of 6 μM in rabbit parietal cell preparation. It is used for the research of gastric ulcers and is also a potent TOPK (T-lymphokine-activated killer cell-originated protein kinase) inhibitor.
- Orally active proton pump inhibitor
- Irreversibly inhibits H+/K+-ATPase
- Used for research of gastric ulcers
- Potent TOPK inhibitor
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Medchemexpress LLC Mitochonic acid 5 | 1354707-41-7 | 99.60% | 329.30 | 100 MG
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Mitochonic acid 5 (MA-5) is a compound that binds to mitochondria, ameliorating renal tubular and cardiac myocyte damage by modulating mitochondrial ATP synthesis independently of oxidative phosphorylation and the electron transport chain. Derived from indole-3-acetic acid, it protects mitochondrial function by regulating energy metabolism and reducing mitochondrial oxidative stress, thus counteracting the effects of mitochondrial dysfunction in various renal diseases.
- Ameliorates renal tubular and cardiac myocyte damage
- Modulates mitochondrial ATP synthesis
- Protects mitochondrial function
- Regulates energy metabolism
- Reduces mitochondrial oxidative stress
- Inhibits TNFα-induced apoptosis in microglia
- Improves renal function in ischemia-reperfusion injury and cisplatin-induced nephropathy models
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Medchemexpress LLC Ribonucleic acid (yeast) | 63231-63-0 | MFCD00132196 | 92.4% | 250 MG
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Ribonucleic acid (yeast) is a research-grade preparation of yeast-derived RNA supplied as a dry biochemical reagent for use in molecular biology and life-science research. It is commonly used as a substrate in enzymatic assays, as a control or blocking nucleic acid in molecular workflows, and as a general-purpose biological material for assay development and validation.
- Provided as a dry material suitable for storage and handling.
- Suitable as substrate for ribonuclease activity and enzymatic studies.
- Useful as a control or blocking nucleic acid in molecular assays.
- Available in multiple pack sizes to support both small-scale and bulk use.
- Characterized with reported purity to aid reproducibility.
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eMolecules 1065267-14-2 | ChemScene | (35-Difluoropyridin-2-yl)methanol | 100mg | 536794068 | CS-0055645 | MFCD11520700 | 145.109 | C6H5F2NO
Pharmablock | cis-2-methoxycarbonylcyclohexanecarboxylic acid | 100mg | 551233527 | PBB0469 | 111955-05-6 | 372.414 | C18H28O8
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