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Filtered Search Results
Medchemexpress LLC 4-[1-(4-hydroxyphenyl)cyclohexyl]phenol | MFCD00019341 | >98.0% | 280.26 | C18H20O2 (13C12) | 1mg
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Bisphenol Z-13C12 is the 13C labeled isotope of Bisphenol Z-13C12 (HY-W770278)[1]
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Medchemexpress LLC Cbz-NH-PEG4-C2-acid | 756526-00-8 | MFCD11041139 | ≥95.0% | 399.44 g·mol⁻¹ | C19H29NO8 | 500 MG
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Cbz-NH-PEG4-C2-acid is a Cbz-protected, PEG-based linker designed for assembly of PROTAC molecules. It couples a four-unit polyethylene glycol spacer with a C2-terminal carboxylic acid and a Cbz-protected amine to enable modular conjugation between ligands and facilitate synthesis workflows.
- Provides a PEG4 spacer for flexible, water-soluble linkage.
- Has a Cbz-protected amine for orthogonal protection and selective deprotection.
- Features a C2-terminal carboxylic acid for amide or ester coupling.
- Optimized for PROTAC synthesis and bioconjugation workflows.
- Suitable for use in standard organic coupling reactions.
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Medchemexpress LLC E/Z-HA155 50mg | 1229652-22-5 | 50 MG
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(E/Z)-HA155 is a boronic acid small-molecule autotaxin (ATX) type I inhibitor supplied as an E/Z isomer mixture for preclinical research. It is used to study cancer, fibrotic diseases, inflammation, pain, and angiogenesis. Supplied as a high-purity solid suitable for biochemical and cell-based assays; recommended storage is powder at -20°C.
- Boronic acid small molecule inhibitor of autotaxin.
- Used in research on cancer, fibrosis, inflammation, pain, and angiogenesis.
- Molecular formula C24H19BFNO5S.
- Molecular weight 463.29 g/mol.
- Purity approximately 99.3%.
- Appearance: solid, off-white to light yellow.
- Recommended storage: powder at -20°C; in solvent keep at -80°C for longer-term, -20°C short-term.
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Medchemexpress LLC (Z)-JQ1-TCO | 2087490-43-3 | 99.3% | 609.18 | 100 MG
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JQ1-TCO (JQ1-trans-cyclooctene) is a derivative of JQ1, an inhibitor of BET. This compound is suitable for click chemistry and can be used as molecular probes in vitro and in vivo. Studies indicate that (Z)-JQ1-TCO does not induce significant degradation of BRD4 in HeLa cells at 10 μM for 18 h.
- Derivative of JQ1, an inhibitor of BET
- Suitable for click chemistry
- Can be used as molecular probes in vitro and in vivo
- Does not induce significant degradation of BRD4 in HeLa cells at 10 μM for 18 h
- Targets BRD4 and the Epigenetic Reader Domain
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Aobchem 2-Fluoro-3-(hydroxymethyl)-5-methylbenzoic acid | ≥95% | CAS 2137681-06-0 | C9H9FO3 | 250mg
2-Fluoro-3-(hydroxymethyl)-5-methylbenzoic acid | ≥95% | CAS 2137681-06-0 | C9H9FO3 | 250mg
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Aobchem (2 4-Dichloro-5-(hydroxymethyl)phenyl)boronic acid | 95% | C7H7BCl2O3 | 250mg
(2 4-Dichloro-5-(hydroxymethyl)phenyl)boronic acid | 95% | C7H7BCl2O3 | 250mg
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Medchemexpress LLC CBZ-NH-PEG4-C2-ACID 10G
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CBZ-NH-PEG4-C2-ACID 10G
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Medchemexpress LLC Z-AZOXYSTROBIN 10 mg
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Z-AZOXYSTROBIN 10MG
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Medchemexpress LLC Z-GLYCINOL 1KG
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Z-GLYCINOL 1KG
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Medchemexpress LLC Z-GLYCINOL 100G
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Z-GLYCINOL 100G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000744587 CBZ-NH-PEG2-C2-ACID 5G
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eMolecules EMOLECULES INC
5000841566 3-CBZ-AMINOMETHYLPHENOL 5G
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eMolecules EMOLECULES INC
5000841221 /--N-CBZ-ALPHA-PHOSPHO 25G
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Medchemexpress LLC Z -3-Nonen-1-ol 1g
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(Z)-3-Nonen-1-ol is an organic compound belonging to the group of alcohols It has a strong floral aroma and is commonly found in a variety of foods including fruits and vegetables (Z)-3-Nonen-1-ol has various applications in the flavor and fragrance industry especially as a fragrance agent in products such as perfumes colognes and air fresheners In addition it has potential utility in inhibiting inflammation-related diseases and cancer
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Medchemexpress LLC 5-Hydroxymethyl-2'-deoxyuridine | 5116-24-5 | >99.9% | 100 MG
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5-Hydroxymethyl-2'-deoxyuridine is a nucleoside analog that has demonstrated inhibitory effects on the replication of various human leukemia cell lines, with IC50 values ranging from 1.7-5.8 μM. It has also been shown to prolong the survival of mice afflicted with L1210 leukemia. This compound is valuable for research into cell replication and leukemia.
- Inhibits replication of human leukemia cell lines.
- Prolongs survival in mouse models of leukemia.
- Useful for research on cell replication.
- Inhibits herpes simplex virus type 1 pyrimidine 2'-deoxyribonucleoside kinase.
- Shows dose-dependent toxicity against a human acute promyelocytic leukemia cell line.
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