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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000724548 RAC-PYROTINIB 100MG
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Medchemexpress LLC (2R,3R)-Firazorexton | 2692692-00-3 | 99.9% | 470.51 g/mol | C22H25F3N2O4S | 5 MG
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(2R,3R)-Firazorexton is an orally active, brain-penetrating orexin type 2 receptor (OX2R) agonist supplied for research use. It is offered as a solid powder and as a DMSO solution for in vitro and preclinical pharmacology studies addressing orexin signaling and narcolepsy-like models.
- Orally active OX2R agonist for pharmacology research.
- Provided as solid powder and 10 mM DMSO solution.
- High purity (~99.85%) suitable for research assays.
- Soluble in DMSO (≈200 mg/mL); ultrasonic assistance may be required.
- Store powder at -20°C; store in solvent at -80°C for extended stability.
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Aobchem AOBCHEM
5000942787 3R 5R 7R -ADAMANTAN-1-YL 3-IS
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Aobchem AOBCHEM
5000943237 2 5-DIETHYLPHENYL PHENYL MET
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![Medchemexpress LLC 1H-1,2,4-triazole-1-ethanol, β-[(4-chlorophenyl)methyl]-α-methyl-α-phenyl-, (αR,βS)- | 259200-30-1 | 99.8% | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000233546.png-250.jpg)
Medchemexpress LLC 1H-1,2,4-triazole-1-ethanol, β-[(4-chlorophenyl)methyl]-α-methyl-α-phenyl-, (αR,βS)- | 259200-30-1 | 99.8% | 10 MG
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(2R,3S)-Brassinazole is the enantiomeric form of brassinazole, a triazole-type inhibitor of brassinosteroid biosynthesis used in plant biology research. It is supplied as a high-purity solid and as a ready-to-use DMSO solution for in vitro and in vivo studies.
- High purity: 99.8% with 100% enantiomeric excess.
- Chemical formula C18H18ClN3O; molecular weight 327.81 g/mol.
- Available as solid (5 mg, 10 mg) and as 10 mM in DMSO solution.
- Highly soluble in DMSO (150 mg/mL); in vivo formulation clear at ≥ 3.75 mg/mL.
- Recommended storage: powder at -20°C or 4°C; in solvent at -80°C or -20°C.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000723720 5-HYDROXYMETHYL-2 -D 1MG
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Apexbio Technology LLC SB 216763 10MG
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SB 216763 10MG APEXBIO TECHNOLOGIES
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Medchemexpress LLC Doxorubicin-SMCC 25mg | 400647-59-8 | 762.76 | C39H42N2O14 | 25 MG
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Doxorubicin-SMCC is a drug-linker conjugate for antibody-drug conjugate (ADC) research that couples the anthracycline topoisomerase II inhibitor doxorubicin to a non-cleavable SMCC linker, producing a stable payload for bioconjugation and preclinical studies.
- Non-cleavable SMCC linker for stable conjugation.
- Acts as a DNA topoisomerase II inhibitor payload.
- Purity 98.8% and molecular weight 762.76.
- Orange to red solid physical form.
- Soluble in DMSO (125 mg/mL); ultrasonic recommended.
- CAS number 400647-59-8 for cross-referencing.
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Medchemexpress LLC E/Z-SIB-1893 | 6266-99-5 | 99.8% | 195.26 g/mol | C14H13N | 25 MG
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(E/Z)-SIB-1893 is the racemic mixture of the (E)- and (Z)-isomers of SIB-1893, a selective, non-competitive antagonist of the metabotropic glutamate receptor subtype 5 (mGluR5). It is provided as a 25 mg research sample with reported molecular formula C14H13N, molecular weight 195.26 g/mol, and purity 99.8%.
- Racemic mixture of E and Z isomers for receptor pharmacology studies.
- Selective non-competitive mGluR5 antagonist useful in mGluR5-related assays.
- High reported purity (99.8%) suitable for in vitro experiments.
- Supplied as a 25 mg quantity for small-scale research applications.
- Molecular formula C14H13N and molecular weight 195.26 g/mol provided for reference.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000428131 TERT-BUTOXYCARBONYL 500G
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Ambeed AMBEED
5000868991 N-BOC- EXO-3-AMINOTROPANE 5GR
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Ambeed AMBEED
5000868999 CIS-4-BOC-AMINOCYCLOHEXYLA 1GR
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eMolecules 157688-46-5 | 2-(1-tert-butoxycarbonyl-4-piperidyl)acetic acid | Pharmablock | MFCD00800239 | 243.303 | C12H21NO4 | 97.000 | CC(C)(C)OC(=O)N1CCC(CC(O)=O)CC1 | 1g | 551059170
2-(1-tert-butoxycarbonyl-4-piperidyl)acetic acid | Pharmablock | 157688-46-5 | MFCD00800239 | 243.303 | C12H21NO4 | 97.000 | CC(C)(C)OC(=O)N1CCC(CC(O)=O)CC1 | 1g | 551059170
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Selleck Chemical LLC Z-Guggulsterone
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Z-Guggulsterone a constituent of Ayurvedic medicinal plant Commiphora mukul inhibits angiogenesis in vitro and in vivo Z-Guggulsterone exhibits anti-inflammatory effects in microglia Z-Guggulsterone induces apoptosis in gastric cancer cells through the intrinsic mitochondria-dependent pathway
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Apexbio Technology LLC Granzyme B Inhibitor Z-AAD-CH2Cl 20ul (10 mM)
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Granzyme B Inhibitor Z-AAD-CH2Cl is a small-molecule inhibitor targeting granzyme B a serine protease predominantly expressed in cytotoxic lymphocytes natural killer (NK) cells and cytotoxic T lymphocytes (CTLs) It is designed to irreversibly inhibit granzyme B activity thereby modulating apoptosis induction and immune regulation Granzyme B Inhibitor Z-AAD-CH2Cl exerts its biological activity primarily through irreversible inhibition of granzyme B In cell-based studies it demonstrates inhibitory activity in models such as NK cell-induced cytotoxicity in chondrocytes lymphocyte-induced caspase-3 activation and DNA fragmentation and activation-induced apoptosis in T-cell populations Based on these pharmacological properties Granzyme B Inhibitor Z-AAD-CH2Cl holds research potential in immunology oncology and inflammation-related disorders
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