Acrylic acids and derivatives
Medchemexpress LLC HY-B1596 50mg Medchemexpress, Ceftizoxime CAS:68401-81-0 Purity:>98%
Medchemexpress, HY-B1596 50mg Ceftizoxime CAS:68401-81-0 Ceftizoxime is a bacterial inhibitor which acts by interfering with bacterial cell wall synthesis and inhibiting cross-linking of the peptidoglycan. 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 Eprosartan | 133040-01-4 | MFCD00897872 | 424.5 g/mol | C23H24N2O4S | 10 MG
Eprosartan is a selective, competitive, orally active angiotensin II receptor antagonist used in research on antihypertensive mechanisms and receptor pharmacology. The compound is typically supplied as a white to off-white crystalline powder for analytical and in vivo studies.
- Selective angiotensin II receptor antagonist with documented receptor binding activity.
- Orally active compound suitable for in vivo pharmacology studies.
- Supplied as a crystalline free base appropriate for analytical and research use.
- Well-characterized in public chemical databases for unambiguous identification.
Apexbio Technology LLC 7ACC1 50995-74-9 100mg
7ACC1 (CAS 50995-74-9) also known as DEAC or Coumarin D1421 is a selective inhibitor of monocarboxylate transporters MCT-1 and MCT-4 which facilitate lactate transmembrane transport By blocking these transporters 7ACC1 disrupts cellular lactate efflux and modulates the metabolic environment of tumor cells In vitro studies demonstrate that treatment with 7ACC1 reduces lactate secretion in renal cancer cells accompanied by decreased cell proliferation migration and invasion as well as downregulation of MCT-1 and MCT-4 protein expression 7ACC1 is a useful tool for investigating tumor metabolism and the mechanisms underlying tumor growth and metastasis
eMolecules 214701-49-2 | 1-(5-Bromopyridin-2-yl)ethanone | Synthonix | MFCD04974523 | 200.035 | C7H6BrNO | 97.000 | CC(=O)c1ccc(Br)cn1 | 250mg | 831793639
1-(5-Bromopyridin-2-yl)ethanone | Synthonix | 214701-49-2 | MFCD04974523 | 200.035 | C7H6BrNO | 97.000 | CC(=O)c1ccc(Br)cn1 | 250mg | 831793639
![eMolecules 1363381-10-5 | Ambeed | 5-Bromopyrazolo[15-a]pyridine-2-carboxylic acid | 50mg | 660581419 | A310230 | MFCD19687637 | 241.044 | C8H5BrN2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502457931.PNG-250.jpg)
eMolecules 1363381-10-5 | Ambeed | 5-Bromopyrazolo[15-a]pyridine-2-carboxylic acid | 50mg | 660581419 | A310230 | MFCD19687637 | 241.044 | C8H5BrN2O2
Medchem Express | LHVS | 5mg | 495800386 | HY-128971 | 170111-28-1 | 527.680 | C28H37N3O5S
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Medchemexpress LLC Bis-acrylate-PEG6 100mg
Bis-acrylate-PEG6 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]
Medchemexpress LLC 2-propenoic acid, homopolymer | 9003-01-4 | MFCD00084394 | 4,000,000 (average) | (C3H4O2)x | 5 G
Poly(acrylic acid) (MW 4,000,000) is a high-molecular-weight anionic polymer supplied as a white to off-white solid for research applications. It is used in biochemical assays and as a corrosion inhibitor and surface stabilizer; preparation and storage guidance are provided in the product datasheet.
- High molecular weight (4,000,000 average)
- White to off-white solid appearance
- Water soluble; recommended 100 mg/mL in H2O with ultrasonic aid
- Used as a corrosion inhibitor and surface stabilizer
- Storage: room temperature for solid; solutions require low-temperature storage
eMolecules 153653-30-6 | Medchem Express | Dofequidar (fumarate) | 5mg | 446268135 | HY-17013A | MFCD00925095 | 597.668 | C34H35N3O7
Medchem Express | Ensartinib (dihydrochloride) | 5mg | 599150329 | HY-103714A | 2137030-98-7 | 634.360 | C26H29Cl4FN6O3
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Medchemexpress LLC HY-13049 5mg Medchemexpress, Cediranib (maleate) CAS:857036-77-2 Purity:>98%
Medchemexpress, HY-13049 5mg Cediranib (maleate) CAS:857036-77-2 Cediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR inhibitor with IC50s of <1, <3, 5, 5, 36, 2 nM for Flt1, KDR, Flt4, PDGFRα, PDGFRβ, c-Kit, 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.
eMolecules 519187-97-4 | Medchem Express | Edonerpic (maleate) | 5mg | 446268790 | HY-17631A | MFCD13152397 | 407.48 | C20H25NO6S
Medchem Express | Edonerpic (maleate) | 5mg | 446268790 | HY-17631A | 519187-97-4 | MFCD13152397 | 407.480 | C20H25NO6S
eMolecules 3614-69-5 | Medchem Express | Dimethindene (maleate) | 5mg | 746319341 | HY-13710A | MFCD00072146 | 408.498 | C24H28N2O4
Ambeed | 1-(26-Diisopropylphenyl)-3-mesityl-45-dihydro-1H-imidazol-3-ium chloride | 1g | 600839316 | A394258 | 866926-59-2 | MFCD17018754 | 384.990 | C24H33ClN2
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eMolecules 81485-25-8 | Medchem Express | Peretinoin | 5mg | 446254726 | HY-100008 | MFCD01742209 | 302.458 | C20H30O2
Medchem Express | Peretinoin | 5mg | 446254726 | HY-100008 | 81485-25-8 | MFCD01742209 | 302.458 | C20H30O2
Medchemexpress LLC TBOPP | 1996629-79-8 | 99.6% | 490.49 | C24H21F3N2O4S | 50MG
TBOPP is a small-molecule research reagent that selectively inhibits DOCK1. It blocks DOCK1-mediated Rac activation with an IC50 of 8.4 μM and binds the DOCK1 DHR-2 domain with a Kd of 7.1 μM. TBOPP has shown anti-tumor activity in preclinical studies and is provided as a high-purity compound with available powder and DMSO solution formats for biochemical and cellular experiments.
- High purity suitable for research applications.
- Selective inhibitor of DOCK1 with IC50 8.4 μM and Kd 7.1 μM.
- Demonstrated anti-tumor activity in preclinical models.
- Available as powder and as a DMSO solution for flexible dosing.
- Comes with supporting documentation such as datasheet, COA, and SDS.
- Stable under recommended cold storage for long-term preservation.
Cayman Chemical OlenolIc AcId Acrylate 10mg
An agonist of 5-HT1A and a derivative of oleanolic acid; acts as an agonist at the 5-HT1A receptor in mouse hippocampal homogenates in a [35S]GTPγS binding assay (EC50 = 0.79 µM); a selective inhibitor of MAO-A over MAO-B (IC50s = 48.8 µM and >100 µM, respectively); reduces immobility in the forced swim test and increases the number of crossings and time spent at the center in the open field test, indicating anti-depressant-like and anxiolytic activities in mice at 10 mg/kg
