Cell Culture Media, Supplements, and Reagents
Sigma Aldrich Fine Chemicals Biosciences G 418 disulfate saltpowder, BioReagent, suitable for cell culture | 108321-42-2 | MFCD00058314 | 1g
G 418 disulfate saltpowder, BioReagent, suitable for cell culture | Mol Wt: 692.71 | 108321-42-2 | MFCD00058314 | 1g
Apexbio Technology LLC Doramectin,5g CAS# 117704-25-3
Doramectin (Dectomax) is a veterinary drug approved by the Food and Drug Administration (FDA) for the treatment of parasites such as gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice and mange mites in cattle. Mutational biosynthetic antiparasitic antibiotic structurally related to the avermectins. Other sizes are also available. Please inqury us for quote.
Medchemexpress LLC HS-243 | 848249-10-5 | 100.0% | C17H16N4O3 | 10MG
HS-243 is a small-molecule research inhibitor of interleukin-1 receptor-associated kinases (IRAKs) with demonstrated anti-inflammatory and anticancer activity. It potently inhibits IRAK-4 (IC50 20 nM) and IRAK-1 (IC50 24 nM), and shows limited off-target activity against TAK1. Supplied for research use only.
- Potent inhibition of IRAK-4 and IRAK-1 (IC50: 20 nM and 24 nM).
- Limited TAK1 inhibition (IC50: ~0.5 μM).
- High reported purity (99.95%).
- Available as solid and DMSO solution formats.
- Suitable for preclinical anti-inflammatory and anticancer studies.
Enzo Life Sciences Decylubiquinone (10mg). CAS: 55486-00-5
Inhibits the Ca2+ dependent mitochondrial permeability transition pore (MPTP) without inhibiting respiration. Maximum effect on Ca2+ retention capacity of rat liver mitochondria at 100μM. Inhibits etoposide-induced apoptosis in in L929 cells at 5μM. Alternative name: 2,3-Dimethoxy-5-methyl-6-decyl-1,4-benzoquinone. Purity: ≥97% (HPLC). Solubility: Soluble in DMSO (10mg/ml). Long Term Storage: -20°C.
eMolecules 2387505-78-2 | Medchem Express | Calhex 231 (hydrochloride) | 5mg | 527574552 | HY-103320A | MFCD22580412 | 443.41 | C25H28Cl2N2O
Ambeed | 6-Bromo-4-chlorothieno[23-d]pyrimidine | 100mg | 552513326 | A100590 | 56844-12-3 | MFCD09264088 | 249.510 | C6H2BrClN2S
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eMolecules 129228-07-5 | AstaTech | 44-BIS(METHOXYMETHYL)-26-DIMETHYLHEPTANE | 0.25g | 281902398 | 12375 | 97 | MFCD07780237 | 216.365 | C13H28O2
Ambeed | 5-Bromo-1-chloro-8-fluoroisoquinoline | 100mg | 596569222 | A734305 | 1501083-37-9 | MFCD22096553 | 260.490 | C9H4BrClFN
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![eMolecules 574-25-4 | 6-MERCAPTOPURINE RIBOSIDE | AstaTech | MFCD00005743 | 284.290 | C10H12N4O4S | 95.000 | OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(S)ncnc12 | 1g | 532133030](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502170176.JPG-250.jpg)
eMolecules 574-25-4 | 6-MERCAPTOPURINE RIBOSIDE | AstaTech | MFCD00005743 | 284.290 | C10H12N4O4S | 95.000 | OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(S)ncnc12 | 1g | 532133030
6-MERCAPTOPURINE RIBOSIDE | AstaTech | 574-25-4 | MFCD00005743 | 284.290 | C10H12N4O4S | 95.000 | OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(S)ncnc12 | 1g | 532133030
Medchemexpress LLC N1-Acetylspermidine hydrochloride | 34450-16-3 | 99.1% | 260.20 | 10 MG
N1-Acetylspermidine hydrochloride is an acetyl derivative of polyamines and acts as a substrate for polyamine oxidase (PAO). It is utilized in colorectal cancer research and can promote apoptosis when combined with Procyanidins.
- Acetyl derivative of polyamines
- Acts as a substrate for polyamine oxidase (PAO)
- Promotes apoptosis when combined with Procyanidins
- Exhibits cleavage efficiency at apurinic sites of DNA
- Useful in colorectal cancer research
Medchemexpress LLC 17-allylamino-17-demethoxygeldanamycin | 75747-14-7 | MFCD04973892 | 99.0% | 585.69 g/mol | C31H43N3O8 | 200 MG
Tanespimycin (17-AAG) is a benzoquinone-derived HSP90 inhibitor used as a research tool in cellular and biochemical studies of HSP90-dependent signaling and oncology models. It displays low-nanomolar potency against HSP90 and is provided in multiple pack formats for laboratory use.
- Potent HSP90 inhibitor with an IC50 of 5 nM.
- Preferential binding to tumor-derived HSP90 compared with normal HSP90.
- Purity 99.01% as supplied.
- Molecular formula C31H43N3O8; molecular weight 585.69 g/mol.
- CAS number 75747-14-7.
- Available as solid and solution formats, including a 200 mg pack.
- Store protected from light; in solvent: -80°C (up to 6 months) or -20°C (up to 1 month).
Medchemexpress LLC HY-107419 5mg Medchemexpress, NU6140 CAS:444723-13-1 Purity:>98%
Medchemexpress, HY-107419 5mg NU6140 CAS:444723-13-1 NU6140 is a selective CDK2-cyclin A inhibitor ( IC 50 , 0.41 μM), exhibits 10- to 36-fold selectivity over other CDKs [1] . NU6140 also potently inhibits Aurora A and Aurora B , with IC 50 s of 67 and 35 nM, respectively [2] . Enhances the apoptotic effect, with anti-cancer activity [1] [2] . 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 HY-107765 5mg Medchemexpress, LY2955303 CAS:1433497-19-8 Purity:>98%
Medchemexpress, HY-107765 5mg LY2955303 CAS:1433497-19-8 LY2955303 is a potent and selective retinoic acid receptor gamma (RARγ) antagonist with a Ki of 1.09 nM. 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 Chloramphenicol 3-acetate | 10318-16-8 | MFCD28898459 | >95.0% | 365.17 | C13H14Cl2N2O6 | 5 MG
Chloramphenicol 3-acetate (CAS 10318-16-8) is the 3-O-acetylated derivative of chloramphenicol used as an intermediate and reference reagent in biochemical and bacterial metabolism studies. Supplied in small research quantities; purity and storage recommendations are detailed in the certificate of analysis.
- Acetylated derivative of chloramphenicol.
- Commonly used as an intermediate in biodegradation and metabolism studies.
- Provided in small research quantities (for example, 1 mg and 5 mg).
- Chemical formula C13H14Cl2N2O6; molecular weight 365.17.
- Certificate of analysis available for purity and storage information.
Apexbio Technology LLC Thonzonium Bromide,50mg CAS# 553-08-2
Thonzonium Bromide is a surface active agent and an inhibitor of V-ATPase proton transport with EC50 value of 69 µM [1] [2].Vacuolar ATPases (V-ATPases) are proton pumps that maintain pH homeostasis. V-ATPases couple the energy of ATP hydrolysis to proton transport across intracellular membranes [2].Thonzonium Bromide is a surface active agent and an inhibitor of V-ATPase proton transport. In wild-type yeast cells, thonzonium bromide significantly decreased the cytosolic pH to 6.22. In vacuolar membrane vesicles, thonzonium bromide inhibited proton transport with EC50 value of 69 µM in a dose-dependent way. However, thonzonium bromide didn’t inhibit ATP hydrolysis, which suggested that thonzonium bromide uncoupled V-ATPase proton pumps. In wild-type yeast cells, thonzonium bromide (1 µM) didn’t inhibit cell growth. Other sizes are also available. Please inqury us for quote.
Sigma Aldrich Fine Chemicals Biosciences Vancomycin hydrochloride from Streptomyces orientalis meets USP testing specifications | 1404-93-9 | 1G
Vancomycin hydrochloride from Streptomyces orientalis meets USP testing specifications | Mol Wt: 1485.71 | 1404-93-9 | 1G
Medchemexpress LLC HZX-02-059 | 2240205-30-3 | 99.4% | 487.48 | 50 MG
HZX-02-059 is a potent methuosis inducer and dual-target PIKfyve/tubulin inhibitor with anticancer activity. Methuosis primarily disrupts the balance of endocytosis and exocytosis, leading to the formation of numerous vesicles and inducing cell death. This compound also induces cell vacuolization, promotes apoptosis, downregulates the p53 pathway, inhibits PI3K/AKT phosphorylation, and inhibits c-Myc and NF-κB transcription.
- Potent methuosis inducer
- Dual-target PIKfyve/tubulin inhibitor
- Anticancer activity
- Induces cell vacuolization
- Promotes apoptosis
- Downregulates the p53 pathway
- Inhibits PI3K/AKT phosphorylation
- Inhibits c-Myc and NF-κB transcription