Pyridines and derivatives
- (4)
- (1)
- (5)
- (5)
- (520)
- (22)
- (2,105)
- (22)
- (2)
- (5)
- (5)
- (271)
- (175)
- (1)
- (14)
- (50)
- (300)
- (86)
- (225)
- (6)
- (4)
- (2)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (5)
- (1)
- (12)
- (4)
- (8)
- (7)
- (12)
- (60)
- (867)
- (5)
- (55)
- (60)
- (58)
- (19)
- (346)
- (2)
- (4)
- (2)
- (1)
- (1)
- (5)
- (275)
- (1)
- (1,700)
- (2)
- (27)
- (7)
- (1)
- (92)
- (4)
- (13)
- (77)
- (128)
- (54)
- (59)
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- (4)
- (1)
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- (4)
- (2)
- (1)
- (5)
- (17)
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- (1)
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- (60)
- (21)
- (1)
- (1)
- (29)
- (49)
- (7)
- (2)
- (1)
- (5)
- (6)
- (12)
- (1)
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- (1)
- (18)
- (1)
- (14)
- (4)
- (1)
- (11)
- (5)
- (1)
- (10)
- (15)
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- (7)
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- (1)
- (4)
- (6)
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- (1)
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- (2)
- (1)
- (15)
- (17)
- (4)
- (2)
- (2)
- (5)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
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- (9)
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- (1)
- (16)
- (7)
- (5)
- (1)
- (1)
- (3)
- (5)
- (10)
- (2)
- (1)
- (6)
- (6)
- (7)
- (12)
- (1)
- (1)
- (39)
- (1)
- (12)
- (11)
- (4)
- (2)
- (2)
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- (1)
- (1)
- (1)
- (2)
- (9)
- (3)
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- (1)
- (1)
- (3)
- (6)
- (3)
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- (1)
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- (1)
- (1)
- (1)
- (3)
- (3)
- (1)
- (6)
- (5)
- (2)
- (1)
- (19)
- (9)
- (1)
- (2)
- (1)
- (1)
- (1)
- (22)
- (22)
- (2)
- (2)
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- (1)
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- (1)
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- (1)
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- (1)
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- (8)
- (6)
- (2)
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- (1)
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- (2)
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- (11)
- (2)
- (2)
- (2)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
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- (1)
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- (544)
- (5)
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- (22)
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- (9)
- (1)
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- (1)
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- (1)
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- (1)
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- (1,015)
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- (1)
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- (904)
- (7)
- (35)
- (7)
- (2)
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- (418)
- (26)
- (4)
- (10)
- (1)
- (1)
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- (1)
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- (6)
- (2)
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- (1)
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- (1)
- (3)
- (19)
- (2)
- (8)
- (72)
- (4)
- (1,561)
- (2)
- (4)
- (12)
- (9)
- (1)
- (14)
- (3)
- (9)
- (3)
- (2)
- (5)
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- (2)
- (1)
- (16)
- (3)
- (13)
- (11)
- (13)
- (10)
- (2)
- (2)
- (1)
- (2)
- (2)
- (408)
- (5)
- (6)
- (2)
- (7)
- (2)
- (3)
- (2)
- (237)
- (3)
- (2)
- (3)
- (18)
- (5)
- (2)
- (264)
- (3)
- (4)
- (4)
- (1)
- (2)
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- (4)
- (1)
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- (5)
- (2)
- (3)
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- (2)
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Filtered Search Results
Medchemexpress LLC Benzamide, 2-((trans-4-hydroxycyclohexyl)amino)-4-(tetrahydro-6,6-dimethyl-4-oxo-indazol-1-yl) | 908112-43-6 | 99.5% | 464.48 g/mol | C23H27F3N4O3 | 1 ML
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SNX-2112 is a small-molecule inhibitor of heat shock protein 90 (Hsp90) used in research applications studying Hsp90-mediated signaling and client protein degradation. It is supplied as a 10 mM solution in DMSO (1 mL) and is also available in multiple solid mass formats for experimental flexibility.
- High purity suitable for research applications, supporting reproducible results.
- Supplied as a ready-to-use 10 mM solution in DMSO for convenient dosing.
- Available in multiple solid formats to support different assay types and scales.
- Molecular weight of 464.48 g/mol for accurate dosing and calculations.
- Commonly used for cell-based assays and biochemical studies of Hsp90 activity.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC PROTAC BRD9 Degrader-4 | 2633632-34-3 | 99.1% | C42H49FN6O7 | 1 MG
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PROTAC BRD9 Degrader-4 is a BRD9 bifunctional degrader for researching cancer. This compound is specifically designed for various cancer research applications.
- Bifunctional BRD9 degrader
- Intended for cancer research applications
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Sigma Aldrich Fine Chemicals Biosciences Melphalan powder100MG
Melphalan also known as L-phenylalanine mustard is an alkylating agent. It belongs to the class of nitrogen mustards which act as chemotherapeutic agents.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC DPTIP | 351353-48-5 | 99.7% | 25 MG
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DPTIP is a potent, brain-penetrant neutral sphingomyelinase 2 (N-SMase 2) inhibitor. It also acts as an exosome inhibitor, demonstrating an IC50 of 30 nM. It is intended for research use only.
- Potent brain penetrant neutral sphingomyelinase 2 (N-SMase 2) inhibitor
- Exosome inhibitor
- IC50 of 30 nM
- Blocks EV secretion in a dose-dependent manner (0.03-30 μM)
- Decreases exosome release by 50% in astrocytes at 30 μM
- Inhibits IL-1β-induced astrocyte-derived EV release in mice (10 mg/kg IP)
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Sigma Aldrich Fine Chemicals Biosciences Rifabutin100MG
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
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Eagle Biosciences Inc Bovine Betacellulin, 100 ug
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Bovine Betacellulin
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Medchemexpress LLC Amidephrine | 37571-84-9 | 97.0% | 244.31 | 25 MG
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Amidephrine is a selective agonist of alpha 1-adrenoceptor. It inhibits monopulse field contraction of the vas deferens epithelium and prostate gland. This product is for research use only and not for sale to patients.
- Selective agonist of alpha 1-adrenoceptor
- Inhibits monopulse field contraction of the vas deferens epithelium and prostate gland
- For research use only
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Medchemexpress LLC Pridopidine | 346688-38-8 | MFCD09835586 | 99.9% | 281.41 | 25 MG
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Pridopidine is identified as a dopamine (DA) stabilizer that functions as a low-affinity dopamine D2 receptor (D2R) antagonist. It exhibits high affinity for the sigma 1 receptor (S1R), with a Ki value between 70 and 80 nM, which is approximately 100 times greater than its affinity for D2R.
- Dopamine (DA) stabilizer
- Low affinity dopamine D2 receptor (D2R) antagonist
- High affinity towards sigma 1 receptor (S1R)
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Medchemexpress LLC Giemsa stain | 51811-82-6 | 5 G
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Giemsa stain is a composite dye comprising methylene azure, methylene blue, eosin, and other components. It is utilized to stain chromatin, nuclear membranes, specific cytoplasmic components, and microorganisms.
- Comprising methylene azure, methylene blue, eosin, and other components.
- Utilized to stain chromatin.
- Stains nuclear membranes.
- Stains specific cytoplasmic components.
- Stains microorganisms.
- Intended for research in cytological and parasitological staining.
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Medchemexpress LLC Afatinib impurity 5 | 402855-03-2 | 25mg
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Afatinib impurity 5 is an impurity of Afatinib (HY-10261)
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Medchemexpress LLC TC-2559 difumarate | 2454492-41-0 | 98.4% | 438.43 | 1 MG
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TC-2559 difumarate is a central nervous system (CNS)-selective, orally active partial agonist of the α4β2 subtype of nicotinic acetylcholine receptors (nAChR).
- Selectivity for α4β2 receptors over α2β4, α4β4, and α3β4 receptors, with EC50 values ranging from 10-30 μM.
- Demonstrates an antinociceptive effect, reducing formalin-induced nociceptive responses in mice and inhibiting chronic constriction injury-induced neuropathic pain in rats.
- Solubility of 43.84 mg/mL (99.99 mM) in H2O, requiring ultrasonic and warming for preparation.
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Apexbio Technology LLC Ramelteon(Synonyms: Rozerem, TAK-375, Ramelteon, Melatonin receptor agonist, MT1/MT2 agonist), 100mg, CAS: 196597-26-9.
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Ramelteon (CAS 196597-26-9) is a potent orally active agonist selective for MT1 and MT2 melatonin receptors Structurally characterized by its S-enantiomer and ether functional group ramelteon exhibits high binding affinity toward MT1 and MT2 receptors with reported Ki values of 14 pM and 112 pM respectively whereas affinity for the MT3 receptor is considerably lower (Ki 2650 nM) By activating MT1 and MT2 receptors ramelteon suppresses cAMP production in human cells expressing these receptors with IC50 values of 21 2 pM/L (MT1) and 53 4 pM/L (MT2) Given its receptor selectivity and minimal side-effect profile ramelteon is frequently utilized in research investigating circadian rhythms and sleep disorders
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Bioss SARS spike glycoprotein S1
SARS spike glycoprotein S1
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Medchemexpress LLC CD117/c-Kit Mouse 50ug
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CD117/c-Kit protein is a tyrosine protein kinase that acts as a cell surface receptor for KITLG/SCF and regulates cell survival proliferation hematopoiesis stem cell maintenance gametogenesis mast cell development migration function and melanogenesis CD117/c-Kit Protein Mouse (HEK293 His) is the recombinant mouse-derived CD117/c-Kit protein expressed by HEK293 with C-10 His labeled tag
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Medchemexpress LLC Ml311 | 315698-17-0 | 99.0% | 415.45 | C23H24F3N3O | 1 MG
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ML311 is a small-molecule research compound that selectively inhibits the Mcl-1/Bim protein-protein interaction and is used in cellular and in vivo pharmacology studies. Reported data show submicromolar cellular potency across multiple cancer cell lines. The product is supplied as a high-purity solid with validated solubility and storage recommendations for preclinical use.
- Potent and selective inhibitor of the Mcl-1/Bim interaction.
- High purity (approximately 99%).
- White to off-white solid suitable for analytical and biological assays.
- DMSO soluble with published in vitro and in vivo formulation protocols.
- Reported submicromolar EC50/GI50 activity across multiple cell lines.
- Packaged in multiple milligram quantities for preclinical studies.
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