Cell Culture Media, Supplements, and Reagents
eMolecules 912789-08-3 | Medchem Express | ISX-3 | 5mg | 785215381 | HY-148694 | 330.77 | C16H15ClN4O2
Medchem Express | ISX-3 | 5mg | 785215381 | HY-148694 | 912789-08-3 | 330.770 | C16H15ClN4O2
eMolecules 136310-64-0 | SCOPINE DI(2-THIENYL) GLYCOLATE | MFCD09038796 | 1g
Medchem Express | Exatecan (mesylate) | 5mg | 446263235 | HY-13631A | 169869-90-3 | MFCD04113012 | 531.560 | C25H26FN3O7S
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool<|a>
Medchemexpress LLC JP1302 dihydrochloride | 1259314-65-2 | MFCD10565599 | >98.0% | 441.40 | C24H26Cl2N4 | 5 MG
JP1302 dihydrochloride is a research-grade small molecule antagonist selective for the α2C-adrenoceptor, supplied as the dihydrochloride salt for improved solubility. It has reported high affinity for human α2C receptors (Kb ≈ 16 nM; Ki ≈ 28 nM) and is used in preclinical studies of neuropsychiatric and renal dysfunction models. Intended for laboratory research use only.
- High affinity α2C-adrenoceptor antagonist (Kb ≈ 16 nM; Ki ≈ 28 nM).
- Dihydrochloride salt form for improved stability and solubility.
- Molecular formula C24H26Cl2N4; molecular weight 441.40.
- Supplied in small research quantities suitable for analytical and preclinical use.
- For laboratory research only; not for human or veterinary use.
Medchemexpress LLC HY-112762A 10mg Medchemexpress, (E)-LHF-535 CAS: Purity:>98%
Medchemexpress, HY-112762A 10mg (E)-LHF-535 CAS: (E)-LHF-535 is the E-isomer of LHF-535. LHF-535 is an antiviral agent extracted from patent WO2013123215A2, Compound 38, has EC50s of <1 μM, <1 μM, <1 μM, and 1-10 μM for Lassa, Machupo, Junin, and VSVg virus, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
![Medchemexpress LLC 2-Thiabicyclo[3.1.0]hexane-4,6-dicarboxylic acid, 4-amino-, 2,2-dioxide, (1R,4S,5S,6S)- | 635318-11-5 | ≥98.0% | C7H9NO6S | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC 2-Thiabicyclo[3.1.0]hexane-4,6-dicarboxylic acid, 4-amino-, 2,2-dioxide, (1R,4S,5S,6S)- | 635318-11-5 | ≥98.0% | C7H9NO6S | 100 MG
LY404039 is a potent, selective, and orally active mGluR2 and mGluR3 agonist. It exhibits >100-fold selectivity for mGluR2/3 over other receptors/transporters and has antipsychotic and anxiolytic effects.
- Potent, selective, and orally active mGluR2 and mGluR3 agonist
- Ki values of 149 nM and 92 nM for mGluR2 and mGluR3
- Exhibits >100-fold selectivity for mGluR2/3 over other receptors/transporters
- Has antipsychotic effects
- Has anxiolytic effects
Medchemexpress LLC HY-B0321 100mg Medchemexpress, Tropicamide CAS:1508-75-4 Purity:>98%
Medchemexpress, HY-B0321 100mg Tropicamide CAS:1508-75-4 Tropicamide (Ro 1-7683) is a selective M4 muscarinic acetylcholine receptor antagonist. Tropicamide produces short acting mydriasis (dilation of the pupil) and cycloplegia when applied as eye drops. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Sigma Aldrich Fine Chemicals Biosciences Kanamycin sulfate from Streptomyces kanamyceticus | 25389-94-0 | MFCD00070253 | 1 g
Kanamycin sulfate from Streptomyces kanamyceticus | Mol Wt: 582.58 | 25389-94-0 | MFCD00070253 | 1 g
Medchemexpress LLC Valproic acid-d6 | 87745-18-4 | MFCD01074058 | 99.8% | 150.25 | C8H10D6O2 | 10 MG
Valproic acid-d6 is a deuterium-labeled analogue of valproic acid used as an internal standard and reference material for analytical, pharmacokinetic, and method development applications. Supplied as a liquid isotopically labeled standard, it provides consistent isotopic enrichment and purity for reliable mass spectrometry and quality-control workflows.
- Deuterium labeled for use as an isotope-dilution internal standard.
- High purity (99.8%) for accurate analytical results.
- Chemical formula C8H10D6O2; molecular weight 150.25.
- Available in small, precise quantities suitable for analytical use.
- Storage stability: pure form stable at -20°C (3 years) or 4°C (2 years).
- Compatible with LC-MS and GC-MS method validation and pharmacokinetic studies.
Apexbio Technology LLC Streptozocin 18883-66-4 500mg
Streptozocin is an antibiotic derivative commonly utilized as an antitumor agent in biomedical research It exerts its biological function primarily through DNA alkylation resulting in targeted cellular toxicity Notably streptozocin selectively acts on pancreatic -cells by depleting intracellular nicotinamide adenine dinucleotide (NAD ) leading to dysregulated glucose metabolism and experimental induction of diabetes mellitus In addition streptozocin is frequently employed in vitro and in vivo to establish diabetic animal models for examination of diabetes-related complications and screening antidiabetic therapies Reported IC50 values vary depending on cell types and conditions with typical values ranging approximately from 11 to 25 M in pancreatic -cell lines
Medchemexpress LLC HY-18649 5mg , BCX 4430 Immucillin-A hydrochloride;Galidesivir hydrochloride CAS:222631-44-9 Purity:98%
Medchemexpress, HY-18649 5mg BCX 4430 Immucillin-A hydrochloride;Galidesivir hydrochloride CAS:222631-44-9 Formula:C11H16ClN5O3 Purity:98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Vu0155041 | 1093757-42-6 | 99.10% | C14H15Cl2NO3 | 50 MG
VU0155041 is a potent, selective positive allosteric modulator (PAM) of mGluR4, with EC50s of 798 nM and 693 nM for human and rat mGluR4, respectively. VU0155041 has potential for the research of Parkinson's disease (PD).
- Potent and selective positive allosteric modulator (PAM) of mGluR4
- EC50s of 798 nM for human mGluR4
- EC50s of 693 nM for rat mGluR4
- Potential for Parkinson's disease research
- Does not affect NMDA receptor currents in striatal medium spiny neurons at 10 μM in vitro
- Reverses catalepsy induced by dopamine D2 receptor antagonist Haloperidol in rats
- Reverses Reserpine-induced akinesia in rats
Abcam Chloramphenicol ß-D-galactoside, 2MG
MW 485.3 Da. Chloramphenicol precursor that releases chloramphenicol upon enzymatic or chemical hydrolysis. Galactose is linked to the site of action of chloramphenicol via a hydrolysable bond.
The product is subject to the following: Abcam Restricted Use Statement
Medchemexpress LLC PF-06380101 (Aur0101) | 1436391-86-4 | MFCD28385873 | 100.0% | 743.01 g/mol | C39H62N6O6S | 100 MG
PF-06380101 (Aur0101) is an auristatin-class microtubule inhibitor and a dolastatin 10 analogue used as a cytotoxic payload in antibody-drug conjugates and for tumor cell proliferation assays. It is supplied as a solid powder for research use only and displays potent antimitotic activity with distinct ADME properties compared with related analogues.
- Auristatin-class microtubule inhibitor with potent antimitotic activity.
- High purity of 99.95%.
- Molecular weight 743.01 g/mol and formula C39H62N6O6S.
- Solid, white to off-white powder appearance.
- Powder stability: -20°C for 3 years, 4°C for 2 years.
- Intended for research use only and preparation of antibody-drug conjugates.
Med Vet International Clindamycin Hcl Capsules, 150mg, 100ct
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Clindamycin HCL capsules are a generic version of Cleocin. It is used to treat a wide variety of bacterial infections and should be stored at room temperature away from light and moisture.
Medchemexpress LLC 6-(4-((5-chloro-4-((4-chlorophenyl)amino)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)-N-hydroxyhexanamide | 2284621-75-4 | 98.5% | 450.32 | C19H21Cl2N7O2 | 50MG
JAK/HDAC-IN-1 is a small-molecule dual inhibitor of Janus kinases and histone deacetylases that exhibits low-nanomolar biochemical potency and antiproliferative, proapoptotic activity in hematological cell lines. The compound includes solubility and storage guidance for research applications and is provided as a high-purity research reagent.
- Dual JAK and HDAC inhibitory activity with low-nanomolar IC50s (example: JAK2 4 nM; HDAC 2 nM).
- Demonstrated antiproliferative and proapoptotic effects in hematological cell lines.
- Molecular formula C19H21Cl2N7O2; molecular weight 450.32.
- Soluble in DMSO (~20.83 mg/mL) and formulatable for in vivo dosing at ≥2.08 mg/mL in recommended vehicles.
- Storage: keep at 4°C protected from light; in solution store at -80°C (6 months) or -20°C (1 month) protected from light.
- Reported purity approximately 98.5%.