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Ethynodiol diacetate is a click chemistry reagent that contains an Alkyne group. It can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. It is for research use only and not sold to patients.
Click chemistry reagent
Contains an Alkyne group
Can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups
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SID7970631 is an isoquinolinone analog that functions as a potent and selective submicromolar SF-1 inhibitor (IC50=255 nM). It can be used for cancer research.
Potent and selective submicromolar SF-1 inhibitor
IC50 of 255 nM (SF-1)
Displays cytotoxic effects on H295R/TR SF-1 cells and SW-13 cells
Powder storage: -20°C for 3 years, 4°C for 2 years
In solvent storage: -80°C for 6 months, -20°C for 1 month
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C-021 is a small-molecule antagonist of the CC chemokine receptor 4 (CCR4) used for research into GPCR signaling and immunology. It inhibits CCR4-mediated chemotaxis in human and mouse systems and is supplied as a solid for laboratory studies.
Target CCR4.
Molecular formula C27H41N5O2.
Molecular weight 467.65 g/mol.
Purity 99.95%.
Appearance solid, off-white to light yellow.
Storage powder: -20°C (up to 3 years); in solvent: -80°C (short-term).
Supplied in small research quantities.
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INX-SM-56 is a cytotoxin used as an antibody-drug conjugate (ADC) payload for the synthesis of anti-VISTA antibody conjugates. It is supplied as a white-to-yellow solid with high analytical purity and is intended for research use.
Cytotoxin for antibody-drug conjugate synthesis.
High purity: 99.47% (analytical).
Molecular weight: 576.70; formula: C32H36N2O6S.
CAS number: 2734878-18-1.
Available in small research sizes such as 1 mg and 5 mg.
Storage: 4°C, sealed, away from moisture and light; in solvent: -80°C (6 months), -20°C (1 month).
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Camelliaside A is a phytochemical that acts as a HER2 ligand. It has been shown to lack antifungal activity against *Rhizoctonia solani* and is applicable to breast cancer-related research.
Phytochemical and HER2 ligand
Shows no inhibitory effect on mycelial growth of *Rhizoctonia solani*
Applicable to breast cancer-related research
Off-white to light yellow solid appearance
Purity of 99.65%
Store at 4°C, protect from light. In solvent: -80°C for 6 months; -20°C for 1 month (protect from light).
Soluble in DMSO (100 mg/mL)
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Nitrofurazone (Nitrofural) is a broad-spectrum, nitro-aromatic antibiotic with oral activity. It is effective against both Gram-positive and Gram-negative bacteria, making it suitable for research into various infections and skin conditions.
Active against Gram-positive and Gram-negative bacteria.
Useful in research for various infections and skin conditions.
Inhibits RNA and ribosomal subunit synthesis.
Can be used to create breast tumor models.
Powder storage: -20°C for 3 years; 4°C for 2 years.
Storage in solvent: -80°C for 2 years; -20°C for 1 year.
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YH-306 is a small-molecule antitumor agent that inhibits focal adhesion kinase (FAK) signaling and reduces cancer cell migration, invasion, and metastasis in preclinical studies.
Inhibits focal adhesion kinase (FAK) signaling and related pathways.
Reduces expression of MMP2 and MMP9.
Inhibits Arp2/3-mediated actin polymerization.
Molecular formula: C19H18N2O2.
Molecular weight: 306.36 g/mol.
Purity: 98.3%.
Appearance: light yellow to light brown solid.
Storage: 4°C, protect from light; in solvent: -80°C (6 months), -20°C (1 month).
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Camelliaside A is a flavonoid isolated from Camellia oleifera seed pomace and supplied as a high-purity research standard for in vitro and in vivo studies.
Flavonoid compound with CAS number 135095-52-2.
Molecular formula C33H40O20 and molecular weight 756.66.
High purity: 99.65% (manufacturer reported).
Soluble in DMSO (100 mg/mL); ultrasonic assistance recommended.
Multiple in vivo formulations documented with ≥2.5 mg/mL solubility.
Storage: product at 4°C protected from light; in solvent: -80°C (6 months) or -20°C (1 month).
Intended for research use only.
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Batabulin sodium is a sodium salt antitumor research compound that covalently and selectively binds specific β-tubulin isotypes, disrupting microtubule polymerization, inducing G2/M cell-cycle arrest, and triggering apoptotic cell death. Supplied as an off-white to light-yellow solid for in vitro and in vivo research applications.
Covalently binds to a subset of β-tubulin isotypes.
Disrupts microtubule polymerization and induces G2/M arrest.
Induces apoptosis in cell-based assays.
High reported purity (~99.8%).
Soluble in DMSO; use freshly opened solvent and ultrasonic assistance if needed.
Store powder at 4°C; in solution store at -80°C for long-term stability.
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Modoflaner is an isophenylamide insecticide intended for research use only. It may act through allosteric regulation of gamma-aminobutyric acid-gated chloride channels.
Isophenylamide insecticide
May act through allosteric regulation of gamma-aminobutyric acid-gated chloride channels
Effectively kills moth, xylophone, and gray planthopper
Prevents female adult ticks from laying eggs or eggs from hatching
White to off-white solid appearance
Purity of 98.26%
Store at 4°C, protected from light; in solvent at -80°C for 6 months or -20°C for 1 month, protected from light
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SRI-37330 hydrochloride is an orally bioavailable small-molecule inhibitor of thioredoxin-interacting protein (TXNIP) used in preclinical metabolic research. It modulates glucagon secretion and signaling, reduces hepatic glucose production, and reverses hepatic steatosis, making it relevant for studies of type 2 diabetes and related metabolic disorders.
Orally bioavailable TXNIP inhibitor.
Modulates glucagon secretion and function.
Reduces hepatic glucose production.
Reverses hepatic steatosis in preclinical models.
High reported purity (99.72%).
Solid form suitable for storage and formulation.
Storage guidance: sealed at 4°C; in solvent, -80°C up to 6 months.
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TCS PrP Inhibitor 13 is a small-molecule antiprion agent that inhibits cellular prion protein (PrPC) and reduces protease-resistant prion accumulation. It is supplied as a solid for research use and shows potent activity in cellular assays (IC50 3 nM).
Chemical formula: C15H11N3O3.
Molecular weight: 281.27.
Purity: 99.7%.
Appearance: solid, white to yellow.
Storage conditions: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
Reported activity: IC50 3 nM in ScN2a and F3 cells.
Biological effect: induces apoptosis in schwannoma cells.
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SID7970631 is an isoquinolinone analog reported as a potent and selective submicromolar inhibitor of Steroidogenic Factor-1 (SF-1) with an IC50 of 255 nM. Supplied as a solid research compound, it is intended for use in studies of SF-1 signaling and cancer-related cellular assays.
Potent SF-1 inhibitor (IC50 255 nM).
Submicromolar activity suitable for cell-based assays.
Solid powder with high purity (98.3%).
Molecular formula C24H24N2O7; molecular weight 452.46 g/mol.
Storage recommendations: powder -20°C long term, 4°C short term; solutions -80°C for months.
Available as small-scale solids and 10 mM solution in DMSO for research use.
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Bliretrigine is a small-molecule sodium channel blocker used in research with reported analgesic effects. The product is provided as a white to off-white solid with specified solubility in DMSO and defined storage recommendations for both powder and solution forms.
Sodium channel blocker with analgesic activity.
Molecular formula C20H24N4O2.
Molecular weight 352.43.
Purity 99.42%.
Appearance white to off-white solid.
Soluble in DMSO at 50 mg/mL; may require ultrasonic assistance.
Store powder at -20°C for up to 3 years or at 4°C for up to 2 years.
Store in solution at -80°C for up to 6 months or at -20°C for up to 1 month.
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