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Filtered Search Results
SANTA CRUZ BIOTECHNOLOGY 1 3-DICHLORO-2-PROPANL-D5 10MG
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NC3652631 1 3-DICHLORO-2-PROPANL-D5 10MG
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AMBEED 2-PYRIDIN-4-YL-1H-IMIDAZ 250MG
NC3661339 2-PYRIDIN-4-YL-1H-IMIDAZ 250MG
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MEDCHEMEXPRESS LLC DOXOFYLLINE 100MG
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501874026 DOXOFYLLINE 100MG
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MEDCHEMEXPRESS LLC CENICRIVIROC MESYLATE 5MG
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501873103 CENICRIVIROC MESYLATE 5MG
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MEDCHEMEXPRESS LLC RAF265 5MG
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501871981 RAF265 5MG
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MEDCHEMEXPRESS LLC D4476 5MG
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501872012 D4476 5MG
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MEDCHEMEXPRESS LLC SALICYL-AMS 5MG
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501872229 SALICYL-AMS 5MG
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MEDCHEMEXPRESS LLC 5 -DEOXYADENOSINE 5MG
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501872484 5 -DEOXYADENOSINE 5MG
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MEDCHEMEXPRESS LLC KIRA6 5MG
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501873758 KIRA6 5MG
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MEDCHEMEXPRESS LLC GSK2636771 5MG
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501873164 GSK2636771 5MG
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Aobchem 1 2-Dimethylimidazole | ≥95% | CAS 1739-84-0 | C5H8N2 | 100g
1 2-Dimethylimidazole | ≥95% | CAS 1739-84-0 | C5H8N2 | 100g
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Medchemexpress LLC 1-Dodecylimidazole | 4303-67-7 | MFCD00278859 | 99.8% | 236.40 | 1 G
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1-Dodecylimidazole is a lysosomotropic detergent and a cytotoxic agent. It induces cell death by accumulating in lysosomes in an acid-dependent manner, disrupting the lysosomal membrane and releasing cysteine proteases into the cytoplasm. The compound also exhibits hypocholesterolaemic activity and broad-spectrum antifungal activity, partly by inhibiting cholesterol biosynthesis.
- Lysosomotropic detergent and cytotoxic agent
- Induces cell death through acid-dependent lysosomal accumulation
- Disrupts lysosomal membranes, releasing cysteine proteases
- Exhibits hypocholesterolaemic activity
- Possesses broad-spectrum antifungal activity
- Shows extracellular pH-dependent cytotoxicity
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eMolecules 1590388-37-6 | (S)-3-(4-CHLOROPHENYL)-BETA-ALANINOL HCL | AstaTech | MFCD13152017 | 222.110 | C9H13Cl2NO | 97.000 | Cl.N[C@@H](CCO)c1ccc(Cl)cc1 | 5g | 112525494
(S)-3-(4-CHLOROPHENYL)-BETA-ALANINOL HCL | AstaTech | 1590388-37-6 | MFCD13152017 | 222.110 | C9H13Cl2NO | 97.000 | Cl.N[C@@H](CCO)c1ccc(Cl)cc1 | 5g | 112525494
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Medchemexpress LLC Thalidomide-NH-CBP/p300 ligand 2 | 2484739-21-9 | 98.6% | C48H57F2N11O6 | 10MG
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Thalidomide-NH-CBP/p300 ligand 2 is a thalidomide-based PROTAC small molecule designed to induce proteasomal degradation of the transcriptional coactivators CBP and p300. It couples a thalidomide-derived E3 ligase recruiting moiety to a CBP/p300-binding ligand and is provided as a light yellow solid for research use.
- Induces proteasomal degradation of CBP and p300.
- Employs a thalidomide-derived E3 ligase recruiting moiety.
- Designed for use in cellular and mechanistic research applications.
- High purity suitable for research (reported ~98.6%).
- Provided as a light yellow solid with molecular weight ~922.03 g·mol⁻¹.
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Medchemexpress LLC Cistanoside A | 93236-42-1 | MFCD01725342 | 99.6% | 800.75 g/mol | C36H48O20 | 10 MG
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Cistanoside A is a phenylethanoid glycoside isolated from Cistanche deserticola with reported nitric oxide (NO)-modulating and anti-inflammatory activity. It is provided as a high-purity research reagent suitable for in vitro and in vivo formulation studies.
- High purity (99.6%) suitable for research applications.
- Phenylethanoid glycoside with reported NO synthase activity.
- Well characterized: CAS 93236-42-1; formula C36H48O20; MW 800.75 g/mol.
- Soluble in DMSO at high concentration; multiple in vivo vehicle options documented.
- Recommended storage -20°C; in solvent stability at -80°C for up to 6 months.
- Supplied in a 10 mg quantity for small-scale experiments.
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