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Filtered Search Results
eMolecules 1065267-14-2 | (3,5-Difluoropyridin-2-yl)methanol | ChemScene | MFCD11520700 | 145.109 | C6H5F2NO | 95.000 | OCc1ncc(F)cc1F | 250mg | 572180426
(3,5-Difluoropyridin-2-yl)methanol | ChemScene | 1065267-14-2 | MFCD11520700 | 145.109 | C6H5F2NO | 95.000 | OCc1ncc(F)cc1F | 250mg | 572180426
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Apexbio Technology LLC 2'-O-Methylguanosine 2140-71-8 250mg
2 -O-Methylguanosine (CAS 2140-71-8) is a modified nucleoside generated enzymatically by tRNA guanosine-2 -O-methyltransferase This compound exhibits biological activity by modulating mRNA translation efficiency and interfering with cell cycle regulation through specific signaling pathways In in vitro studies 2 -O-Methylguanosine has been shown to induce apoptosis making it a valuable molecular tool in cancer research It is frequently utilized to investigate apoptosis induction mechanisms and to support the development of novel therapeutic approaches for related diseases
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![eMolecules 62208-68-8 | Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione | MFCD00788168 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502132261.JPG-250.jpg)
eMolecules 62208-68-8 | Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione | MFCD00788168 | 1g
Ambeed | Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione | 1g | 524988738 | A103238 | 62208-68-8 | MFCD00788168 | 202.169 | C10H6N2O3
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eMolecules 2152628-33-4 | Selpercatinib | Ambeed525.613 | C29H31N7O3 | 99.000 | COc1ccc(CN2C3CC2CN(C3)c2ccc(cn2)-c2cc(OCC(C)(C)O)cn3ncc(C#N)c23)cn1 | 250mg | 837386304
Selpercatinib | Ambeed | 2152628-33-4525.613 | C29H31N7O3 | 99.000 | COc1ccc(CN2C3CC2CN(C3)c2ccc(cn2)-c2cc(OCC(C)(C)O)cn3ncc(C#N)c23)cn1 | 250mg | 837386304
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Apexbio Technology LLC HLCL-61 1158279-20-9 10mg
HLCL-61 (CAS 1158279-20-9) is a selective inhibitor of protein arginine methyltransferase 5 (PRMT5) an enzyme implicated in the epigenetic regulation of gene expression through symmetric dimethylation of arginine residues on histones and other proteins HLCL-61 shows specificity for PRMT5 exhibiting no inhibitory activity against PRMT1 PRMT4 or other type II PRMT family members In cellular studies HLCL-61 suppresses symmetric dimethylation of histones H3 and H4 leading to reduced viability and enhanced differentiation of acute myeloid leukemia (AML) cell lines and primary blasts HLCL-61 is currently utilized in preclinical research to investigate PRMT5-mediated epigenetic mechanisms in cancer
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eMolecules 510758-28-8 | TBTA | Broadpharm | MFCD09265124 | 530.640 | C30H30N10 | 98.000 | C(N(Cc1cn(Cc2ccccc2)nn1)Cc1cn(Cc2ccccc2)nn1)c1cn(Cc2ccccc2)nn1 | 250mg | 649281959
TBTA | Broadpharm | 510758-28-8 | MFCD09265124 | 530.640 | C30H30N10 | 98.000 | C(N(Cc1cn(Cc2ccccc2)nn1)Cc1cn(Cc2ccccc2)nn1)c1cn(Cc2ccccc2)nn1 | 250mg | 649281959
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Medchemexpress LLC N-Carbamoyl-DL-aspartic acid | 923-37-5 | 99.9% | 10 MG
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N-Carbamoyl-DL-aspartic acid, also known as Ureidosuccinic acid, is a precursor of nucleic acid pyrimidines with reported antitumor activities. It has been shown to inhibit antitumor activity and toxicity induced by N-phosphonacetyl-L-aspartate (PALA) in a murine Lewis lung carcinoma model.
- Precursor of nucleic acid pyrimidines
- Exhibits antitumor activities
- Identified for use as laboratory chemical
- Stable under recommended storage conditions
- White to off-white solid appearance
- For research use only
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eMolecules 2435-50-9 | Pyrimidine-4-carbaldehyde | Ambeed | MFCD03789624 | 108.100 | C5H4N2O | 95.000 | O=Cc1ccncn1 | 1g | 600838434
Pyrimidine-4-carbaldehyde | Ambeed | 2435-50-9 | MFCD03789624 | 108.100 | C5H4N2O | 95.000 | O=Cc1ccncn1 | 1g | 600838434
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![eMolecules 17768-41-1 | Adamantan-1-ylmethanamine | ChemScene165.280 | C11H19N | 98.000 | NCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2 | 250mg | 572291386](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000127277.jpg-250.jpg)
eMolecules 17768-41-1 | Adamantan-1-ylmethanamine | ChemScene165.280 | C11H19N | 98.000 | NCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2 | 250mg | 572291386
Adamantan-1-ylmethanamine | ChemScene | 17768-41-1165.280 | C11H19N | 98.000 | NCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2 | 250mg | 572291386
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Medchemexpress LLC Monomethyl auristatin E intermediate-11 | 870640-62-3 | 98.8% | C14H23NO | 250 MG
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Monomethyl auristatin E intermediate-11 is an intermediate reactant used in the synthesis of Monomethyl auristatin E (HY-15162). Monomethyl auristatin E (MMAE) acts as a microtubule/tubulin inhibitor and exhibits anticancer activity. MMAE is commonly utilized as the cytotoxic component (ADC Cytotoxin) in antibody-drug conjugates (ADCs).
- Intermediate reactant in Monomethyl auristatin E synthesis
- Monomethyl auristatin E (MMAE) acts as a microtubule/tubulin inhibitor
- Exhibits anticancer activity
- Utilized as cytotoxic component in antibody-drug conjugates (ADCs)
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Medchemexpress LLC m-PEG8-azide | 869718-80-9 | 250 MG
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m-PEG8-azide is a PEG-based PROTAC linker used in the synthesis of PROTACs. It functions as a click chemistry reagent containing an Azide group, enabling specific reactions with other molecular groups.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Enables strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Relevant for cancer research and targeted therapy applications
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Medchemexpress LLC Mesosulfuron-methyl | 208465-21-8 | 98.0% | 250 MG
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Mesosulfuron-methyl is a sulfonylurea herbicide that functions by inhibiting acetolactate synthase (ALS), and it is used in research for post-emergence control of ryegrass and *Avena spp.* (wild oat) in wheat fields.
- It is a sulfonylurea herbicide.
- It inhibits acetolactate synthase (ALS).
- It is used for post-emergence control.
- It targets ryegrass and *Avena spp.* (wild oat).
- Its application is in wheat fields.
- It is intended for research use only.
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Medchemexpress LLC Menadione (Standard) | 58-27-5 | 99.91% | 250 MG
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Menadione (Standard) is the analytical standard of Menadione, intended for research and analytical applications. It is a naphthoquinone that is converted into active vitamin K2 in the body. Menadione is a potential anticancer agent and radiosensitizer.
- Used for research and analytical applications
- Converted into active vitamin K2 in the body
- Potential anticancer agent
- Potential radiosensitizer
- Commonly used in HPLC, GC, and MS experiments
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Medchemexpress LLC Fenclonine hydrochloride | 23633-07-0 | 98.6% | 236.10 g/mol | C9H11Cl2NO2 | 250mg
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Fenclonine hydrochloride is a selective and irreversible tryptophan hydroxylase inhibitor which is a rate-limiting enzyme in the biosynthesis of serotonin Fenclonine hydrochloride can be used in carcinoid syndrome research[1][2][3]
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eMolecules 3326-32-7 | FITC | Ambeed | MFCD00005063 | 389.380 | C21H11NO5S | 95.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 250mg | 596567711
FITC | Ambeed | 3326-32-7 | MFCD00005063 | 389.380 | C21H11NO5S | 95.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 250mg | 596567711
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