Pyridines and derivatives
- (4)
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- (1)
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- (1)
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- (1)
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Filtered Search Results
U.S. Pharmacopeia Pyridoxine Hydrochloride, 58-56-0, MFCD00012807, 200mg
Molecular formula C8-H12-Cl-N-O3, Molecular weight 205.64 g/mol, Melting Point 401 - 413.6 °F (205 - 212 °C) (decomposes), Synonyms: Vitamin B6 hydrochloride; Pyridoxol hydrochloride
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Chem Service Inc (S)-Nicotine | 54-11-5 | MFCD00006369 | 1g
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This item has a minimum order quantity of 2 per supplier requirements
(S)-Nicotine | MW: 162.23 | 54-11-5 | MFCD00006369 | 1g
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Medchemexpress LLC 5-FLUOROURACIL
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5-Fluorouracil, 1ML
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Promega Corporation PROMEGA CORPORATION
PRA9303 A934
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Ambeed AMBEED
NC3992888 5-BROMOISOPHTHALONITRILE 25G
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Promega Corporation LUMIT DETECTION REAGENT B
PRVB4050 LUMIT DETECTION REAGENT B
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NC3976756 5G 5-BROMOISOPHTHALONITRILE
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Promega Corporation SIRPALPHACD47 BLOCKADE BIOASS
PRJA4801 SIRPALPHACD47 BLOCKADE BIOASS
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Promega Corporation CONTROL AB
PRGA1130 CONTROL AB
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Promega Corporation GOTAQ R ENDURE QPCR MASTER MI
PRA6220 GOTAQ R ENDURE QPCR MASTER MI
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Sigma Aldrich Fine Chemicals Biosciences BROMPHENIRAMINE MALEATE, 1.0 M
Brompheniramine Maleate, 1.0 mg/mL as free base
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Promega Corporation DEHYDROGENASEGLO DETECTION SY
PRJ9010 DEHYDROGENASEGLO DETECTION SY
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Medchemexpress LLC 1-[2-chloro-4-(6,7-dimethoxyquinazolin-4-yl)oxyphenyl]-3-propylurea | 286370-15-8 | 99.5% | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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KRN-633 is a small-molecule vascular endothelial growth factor receptor (VEGFR) inhibitor used in research to study angiogenesis and kinase signaling. It inhibits VEGFR1, VEGFR2, and VEGFR3 with reported IC50 values of 170, 160, and 125 nM, respectively, and has demonstrated activity against c-Kit and PDGFR-β in cellular assays and antitumor effects in xenograft models.
- Inhibits VEGFR1, VEGFR2, and VEGFR3 (IC50 = 170, 160, 125 nM).
- Blocks VEGFR phosphorylation and VEGF-driven endothelial cell proliferation.
- High purity (99.5%) and solid, white to off-white appearance.
- Available in multiple quantities, including small-scale mg vials and ready-to-use DMSO solutions.
- Recommended storage: powder at -20 °C or 4 °C; solutions at -80 °C or -20 °C.
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Medchemexpress LLC Glucagon-like peptide 1 (1-37), human | 87805-34-3 | 99.7% | 4169.48 | 10 MG
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Glucagon-like peptide 1 (1-37), human is a highly potent agonist of the GLP-1 receptor. It is produced by the posttranslational processing of proglucagon and acts as a regulator of various homeostatic events.
- Highly potent agonist of the GLP-1 receptor.
- More stable than GLP-1(7-37), with 94.7% remaining after 4-hour mouse serum exposure.
- Decreases glycemic excursion in a dose-dependent manner.
- Significantly reduces blood glucose levels at 15 and 30 minutes compared to the control group.
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Apexbio Technology LLC PF 1022A 133413-70-4 10mg
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PF 1022A (CAS 133413-70-4) is a cyclodepsipeptide exhibiting anthelmintic activity targeting latrophilin-like transmembrane receptors and nematode GABA receptor pathways It acts by interacting with these receptors affecting pharyngeal muscle activity in nematodes and modulating mammalian proteins such as p53 bax and p21 thereby impacting cell cycle regulation and apoptosis PF 1022A primarily exerts its biological activity as an ionophore facilitating ion transport across membranes In livestock experimental models PF 1022A demonstrates anthelmintic effects at doses of 1 10 mg/kg though precise IC50 values have not been established Based on these characteristics PF 1022A holds research potential in veterinary nematode control and as a tool for studying cell cycle regulation and apoptosis in vascular smooth muscle disease
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