Oxazoles
eMolecules 5780-66-5 | Pyrazine-2-carboxaldehyde | Advanced ChemBlocks | MFCD02179278 | 108.100 | C5H4N2O | 97.000 | O=Cc1cnccn1 | 500mg | 866993624
Pyrazine-2-carboxaldehyde | Advanced ChemBlocks | 5780-66-5 | MFCD02179278 | 108.100 | C5H4N2O | 97.000 | O=Cc1cnccn1 | 500mg | 866993624
Medchemexpress LLC 4-(Chloromethyl)-7-hydroxycoumarin | 25392-41-0 | 98.01% | C10H7ClO3 | 1 ML
4-(Chloromethyl)-7-hydroxycoumarin is a hydroxycoumarin derivative exhibiting potent antioxidant effects and high hydroxyl radical-scavenging properties. It contains a methyl group and a chlorine group within its heterocyclic ring and has been investigated as a potent inhibitor of zinc enzyme carbonic anhydrase isoforms CA IX and XII.
- Potent antioxidant effect
- High hydroxyl radical-scavenging property
- Investigated as inhibitors of tumor-associated carbonic anhydrase isoforms CA IX and XII
Medchemexpress LLC 2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride | 72830-09-2 | 99.7% | 224.08 | 50 G
2-(Chloromethyl)-3,4-dimethoxypyridine hydrochloride is a biochemical reagent suitable for use as a biological material or organic compound in life science-related research. It is intended for research use only and is not sold to patients.
- Biochemical reagent
- Suitable for life science related research
Medchemexpress LLC (2S,4S)-1-tert-butyl 2-methyl-4-hydroxypiperidine-1,2-dicarboxylate | 254882-14-9 | 99.7% | 259.30 | 1 G
AN-12-H5 intermediate-1 ((2S,4S)-1-tert-butyl 2-methyl-4-hydroxypiperidine-1,2-dicarboxylate) is an intermediate of the viral inhibitor AN-12-H5 and can be used to synthesize Antibody-Drug Conjugates (ADCs).
- Intermediate for viral inhibitor AN-12-H5.
- Used to synthesize Antibody-Drug Conjugates (ADCs).
- Targets replication processes of PV and enterovirus 71 (EV71).
- Shows no inhibitory effect on PI4KB activity.
- Moderate inhibitory effects on PI 3-kinase activity.
Medchemexpress LLC VISTA/B7-H5 Rat HE 500ug
VISTA/B7-H5 protein an immunoregulatory receptor inhibits T-cell response and may regulate embryonic stem cell differentiation by inhibiting BMP4 signaling It also stimulates MMP14-mediated MMP2 activation suggesting a role in matrix metalloproteinase processes These roles highlight the significance of VISTA/B7-H5 in immune regulation embryonic development and extracellular matrix dynamics VISTA/B7-H5 Protein Rat (HEK293 Fc) is the recombinant rat-derived VISTA/B7-H5 protein expressed by HEK293 with C-hFc labeled tag
Medchemexpress LLC Pomalidomide-CO-C5-Br | 2227423-38-1 | 450.28 | 250 MG
Pomalidomide-CO-C5-Br is a conjugated compound derived from the E3 ligand Pomalidomide and a linker. It is designed for synthesizing highly effective PROTAC molecules, specifically those targeting ADC. This product is intended for research use only.
- Conjugated E3 ligand Pomalidomide compound.
- Used to synthesize PROTAC molecules.
- Targets ADC.
- Available as a solid, white to light yellow in appearance.
- Stable for 3 years at -20°C as powder.
- Stable for 6 months at -80°C in solvent.
![eMolecules ChemScene Benzo[d]oxazole-5-carboxylic acid 250mg 572177270 CS-0043853 0 000 15112-41-1 MFCD09954950 163 132 C8H5NO3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000127257.jpg-250.jpg)
eMolecules ChemScene Benzo[d]oxazole-5-carboxylic acid 250mg 572177270 CS-0043853 0 000 15112-41-1 MFCD09954950 163 132 C8H5NO3
ChemScene Benzo[d]oxazole-5-carboxylic acid 250mg 572177270 CS-0043853 0 000 15112-41-1 MFCD09954950 163 132 C8H5NO3
Medchemexpress LLC An-12-h5 | 1193340-31-6 | 98.0% | 100 MG
An antienterovirus compound that inhibits replication of poliovirus (PV) and enterovirus 71 (EV71). Supplied as a high-purity solid research reagent, it is suitable for in vitro assays and can be formulated for in vivo dosing following the provided protocols.
- Targets replication of poliovirus and enterovirus 71.
- High purity: 98.0%.
- Molecular weight 513.65 g·mol⁻¹; formula C24H23N3O4S3.
- Soluble in DMSO (100 mg/mL) for in vitro applications.
- Available in solid packages including 100 mg and as a 10 mM solution in DMSO.
- Storage guidance provided for powder and solutions to preserve stability.
![Medchemexpress LLC N-((6aS,8S)-2-[4-(methylthio)phenyl]-6,12-dioxopyrido-benzodiazepin-8-yl)-2-thiophenesulfonamide | 1193340-31-6 | 98.0% | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234736.png-250.jpg)
Medchemexpress LLC N-((6aS,8S)-2-[4-(methylthio)phenyl]-6,12-dioxopyrido-benzodiazepin-8-yl)-2-thiophenesulfonamide | 1193340-31-6 | 98.0% | 1 MG
AN-12-H5 is a research-stage antienterovirus small molecule that inhibits replication of poliovirus (PV) and enterovirus 71 (EV71). Supplied as an off-white to light yellow solid, it is accompanied by quality documentation for research use.
- Antienterovirus activity targeting replication of PV and EV71.
- Purity 98.0% by HPLC.
- Molecular weight 513.65 g/mol; formula C24H23N3O4S3.
- Available in milligram quantities with certificate of analysis and safety data sheet.
- Off-white to light yellow solid; store refrigerated as recommended.
Medchemexpress LLC 1,2-Piperidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) 2-methyl ester, (2S,4S)- | 254882-14-9 | 99.7% | 259.30 | 250 MG
AN-12-H5 intermediate-1 is an intermediate of the viral inhibitor AN-12-H5. It can be used to synthesize Antibody-Drug Conjugates (ADCs). AN-12-H5 is an antienterovirus compound that targets the replication processes of PV and enterovirus 71 (EV71). AN-12-H5 shows no inhibitory effect on PI4KB activity and only moderate inhibitory effects on PI 3-kinase activity.
- Targets the replication processes of PV and enterovirus 71
- Shows no inhibitory effect on PI4KB activity
- Can be used to synthesize antibody-drug conjugates (ADCs)
eMolecules 2385363-22-2 | 5-Bromo-oxazole-2-carboxylic acid methyl ester | J & W PharmLab LLC205.995 | C5H4BrNO3 | 95.000 | COC(=O)c1ncc(Br)o1 | 1g | 553408715
5-Bromo-oxazole-2-carboxylic acid methyl ester | J & W PharmLab LLC | 2385363-22-2205.995 | C5H4BrNO3 | 95.000 | COC(=O)c1ncc(Br)o1 | 1g | 553408715
![Medchemexpress LLC N-(octahydrobenzo[e]pyrido[1,2-a]diazepin-8-yl)thiophene-2-sulfonamide | 1193340-31-6 | 98.0% | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000230745.png-250.jpg)
Medchemexpress LLC N-(octahydrobenzo[e]pyrido[1,2-a]diazepin-8-yl)thiophene-2-sulfonamide | 1193340-31-6 | 98.0% | 10 MG
AN-12-H5 is a small-molecule antienterovirus research compound that inhibits replication of poliovirus (PV) and enterovirus 71 (EV71). It is supplied as a solid or as a DMSO solution and is intended for laboratory research use only.
- Targets viral replication of PV and EV71.
- High purity (≈98%).
- Soluble in DMSO (100 mg/mL); ultrasonic recommended.
- Provided as solid or pre-dissolved DMSO solution for convenient use in assays.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC (S)-1-tert-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate | 756486-14-3 | MFCD12547027 | 97.0% | 257.28 g/mol | C12H19NO5 | 250 MG
AN-12-H5 intermediate-2 (CAS 756486-14-3) is a synthetic small-molecule intermediate used in the synthesis of the viral inhibitor AN-12-H5 and as a building block for antibody-drug conjugate (ADC) development. It is supplied as a solid with reported purity ≥97.0% and is intended for research and medicinal chemistry applications.
- High purity: ≥97.0%.
- Solid form supplied in small research pack sizes.
- Intended application: intermediate for small-molecule synthesis and ADC preparation.
- Typical pack sizes: 50 mg-1 g (research quantities).
- Storage guidance: pure form typically stored at -20°C; in solvent at -80°C.
Medchemexpress LLC Mal-C5-N-bis(PEG2-C2-acid) | 3026691-12-0 | 96.3% | 530.57 | C24H38N2O11 | 25mg
Mal-C5-N-bis(PEG2-C2-acid) is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]