Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Duloxetine Related Compound H United States Pharmacopeia (USP) Reference Standard | 199191-66-7 | 30MG
Duloxetine Related Compound H United States Pharmacopeia (USP) Reference Standard | Mol Wt: 397.49 | 199191-66-7 | 30MG
Selleck Chemical LLC Diclofenac Potassium S3062-50mg
Diclofenac potassium (CGP-45840B) is a nonsteroidal anti-inflammatory drug taken to reduce inflammation and as an analgesic reducing pain in certain conditions
Medchemexpress LLC Edoxaban impurity 63 | 10mg
Edoxaban Impurity 63 is an impurity of Edoxaban (HY-10264)
![eMolecules 183133-96-2 | CABAZITAXEL | AstaTech | MFCD18827611 | 835.944 | C45H57NO14 | 98.000 | CO[C@H]1C[C@H]2OC[C@@]2(OC(C)=O)[C@H]2[C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c4ccccc4)C(C)=C([C@@H](OC)C(=O)[C@]12C)C3(C)C | 0.25g | 484551615](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000488876.jpg-250.jpg)
eMolecules 183133-96-2 | CABAZITAXEL | AstaTech | MFCD18827611 | 835.944 | C45H57NO14 | 98.000 | CO[C@H]1C[C@H]2OC[C@@]2(OC(C)=O)[C@H]2[C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c4ccccc4)C(C)=C([C@@H](OC)C(=O)[C@]12C)C3(C)C | 0.25g | 484551615
CABAZITAXEL | AstaTech | 183133-96-2 | MFCD18827611 | 835.944 | C45H57NO14 | 98.000 | CO[C@H]1C[C@H]2OC[C@@]2(OC(C)=O)[C@H]2[C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c4ccccc4)C(C)=C([C@@H](OC)C(=O)[C@]12C)C3(C)C | 0.25g | 484551615
Medchemexpress LLC D-phenylalanine, 3-(methylsulfonyl)-, phenylmethyl ester, hydrochloride | 2049127-88-8 | 5g
Lifitegrast impurity 4 hydrochloride is an impurity of Lifitegrast (HY-19344)
Medchemexpress LLC Dodecyl gallate | 1166-52-5 | MFCD00002195 | 100.0% | 338.44 g/mol | C19H30O5 | 25G
Dodecyl gallate (lauryl gallate) is an alkyl gallate antioxidant used as a preservative and research reagent in food, pharmaceutical, and cosmetic applications. It is a white to off-white solid with reported antibacterial activity against Gram-positive bacteria and reported antiviral activity against African swine fever virus; commonly used in formulation, stability, and antimicrobial studies.
- Antioxidant properties useful for formulation and stability testing.
- Reported antibacterial activity against Gram-positive bacteria.
- Reported antiviral activity relevant to veterinary research.
- High reported purity for reproducible experimental results.
- Available in laboratory-scale package sizes for research use.
Medchemexpress LLC Flavopiridol (Alvocidib) | 146426-40-6 | 99.4% | 401.84 | 100 MG
Flavopiridol (Alvocidib) is a broad-spectrum and competitive inhibitor of cyclin-dependent kinases (CDKs), effectively inhibiting CDK1, CDK2, and CDK4. It induces a distinct pattern of ER stress in CLL cells, contributing to cell death through IRE1-mediated activation of ASK1 and potentially downstream caspases. This compound also leads to potent upregulation of several primary response genes (PRGs) with both immediate and long-term effects on their expression. Furthermore, Flavopiridol inhibits cyclin E1 and induces apoptosis.
- Broad-spectrum and competitive inhibitor of CDKs
- Inhibits CDK1, CDK2, and CDK4
- Induces ER stress in CLL cells
- Contributes to cell death via IRE1-mediated activation of ASK1
- Upregulates primary response genes
- Inhibits cyclin E1
- Induces apoptosis
Medchemexpress LLC Ticagrelor impurity 5 | 1863036-49-0 | >99.7% | C₂₆H₃₂F₂N₆O₅S | 1 MG
Ticagrelor impurity 5 is an impurity of Ticagrelor (HY-10064) with a molecular weight of 578.63 and a purity of >99.66%. It appears as an off-white to yellow solid and is stable under recommended storage conditions.
- Impurity of Ticagrelor
- Chemical formula C₂₆H₃₂F₂N₆O₅S
- CAS number 1863036-49-0
- Appearance as an off-white to yellow solid
- Stable under recommended storage conditions
- Store at 4°C, stored under nitrogen
- In solvent, store at -80°C for 6 months or -20°C for 1 month, stored under nitrogen
- Shipping at room temperature if less than 2 weeks
Medchemexpress LLC 4-quinazolinamine, N-(3-chloro-2-fluorophenyl)-7-methoxy-6-nitro | 1454307-45-9 | 25mg
Dacomitinib impurity 14 is an impurity of Dacomitinib (HY-13272)
Medchemexpress LLC N-Acetyl mesalazine | 51-59-2 | 99.9% | C9H9NO4 | 50 MG
N-Acetyl mesalazine is the primary intestinal metabolite of 5-Aminosalicylic Acid and serves as a biomarker for evaluating the efficacy of 5-Aminosalicylic Acid. It is utilized in the study of diseases such as colitis and colon cancer, demonstrating its ability to scavenge free radicals, reduce DNA base hydroxylation, and ameliorate mucosal inflammation.
- Functions as a biomarker for 5-Aminosalicylic Acid efficacy
- Scavenges free radicals and reduces DNA base hydroxylation
- Ameliorates mucosal inflammation
- Useful for studying diseases like colitis and colon cancer
Medchemexpress LLC Capecitabine-d11 | 1132662-08-8 | 99.9% | C15H11D11FN3O6 | 1 MG
Capecitabine-d11 is the deuterium labeled Capecitabine. Capecitabine is an oral proagent that is converted to its active metabolite, 5-FU, by thymidine phosphorylase. It is for research use only.
- This compound can be used as a tracer.
- This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC Glycopyrrolate | 596-51-0 | 99.93% | 398.33 | 25MG
Glycopyrrolate (Glycopyrronium bromide) is a quaternary ammonium derivative and a muscarinic receptor antagonist. It has a bronchoprotective effect and produces a beneficial effect on blood pressure. It can be used for the research of bronchial diseases.
- Functions as a muscarinic receptor antagonist.
- Exhibits a bronchoprotective effect.
- Produces a beneficial effect on blood pressure.
- Can be utilized for research related to bronchial diseases.
Medchemexpress LLC Atazanavir | 198904-31-3 | MFCD09839958 | >98% | 704.86 | 50 MG
Atazanavir (BMS-232632) is a highly selective and orally active HIV-1 protease inhibitor. Atazanavir is a substrate and inhibitor of CYP3A4, and an inhibitor of P-glycoprotein (P-gp). Atazanavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM. Atazanavir inhibits cardiac fibrosis, hyperlipidemia and induces malignant glioma death.
- HIV-1 protease inhibitor.
- Substrate and inhibitor of CYP3A4.
- Inhibitor of P-glycoprotein (P-gp).
- SARS-CoV 3CLpro inhibitor (IC50 = 3.49 μM).
- Inhibits cardiac fibrosis and hyperlipidemia.
- Induces malignant glioma death.
Medchemexpress LLC Pantoprazole sodium hydrate | 164579-32-2 | 99.9% | 432.37 | 250 MG
Pantoprazole sodium hydrate is an orally active and potent proton pump inhibitor (PPI). It is a substituted benzimidazole and a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. It improves pH stability and has anti-secretory and anti-ulcer activities. When combined with Doxorubicin, Pantoprazole sodium hydrate significantly increased tumor growth delay.
- Potent proton pump inhibitor
- Improves pH stability
- Possesses anti-secretory activities
- Exhibits anti-ulcer activities
- Can increase tumor growth delay when combined with Doxorubicin
![Medchemexpress LLC 1H-Benzimidazole, 6-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]- | 119141-88-7 | 96.5% | 345.42 | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000385914-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 1H-Benzimidazole, 6-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]- | 119141-88-7 | 96.5% | 345.42 | 1 ML
Esomeprazole is a potent and orally active proton pump inhibitor that reduces acid secretion by inhibiting the H+, K+-ATPase in gastric parietal cells. It is used for symptomatic gastroesophageal reflux disease research.
- Potent and orally active proton pump inhibitor
- Reduces acid secretion by inhibiting H+, K+-ATPase
- Used for symptomatic gastroesophageal reflux disease research