Drug Standards
eMolecules 496775-62-3 | Eltrombopag olamine | Combi-Blocks | MFCD22380664 | 564.643 | C29H36N6O6 | 97.000 | NCCO.NCCO.CC1=NN(C(=O)\C1=N/Nc1cccc(-c2cccc(c2)C(O)=O)c1O)c1ccc(C)c(C)c1 | 1g | 495744847
Eltrombopag olamine | Combi-Blocks | 496775-62-3 | MFCD22380664 | 564.643 | C29H36N6O6 | 97.000 | NCCO.NCCO.CC1=NN(C(=O)\C1=N/Nc1cccc(-c2cccc(c2)C(O)=O)c1O)c1ccc(C)c(C)c1 | 1g | 495744847
Medchemexpress LLC Sofosbuvir impurity B | 96.20% | 529.45 | 5 MG
Sofosbuvir impurity B is an impurity of Sofosbuvir. Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrating potent anti-hepatitis C virus (HCV) activity.
- Active inhibitor of HCV RNA replication
- Potent anti-hepatitis C virus (HCV) activity
- Supplied as a white to off-white solid
Chemie Tek BINIMETINIB MEK162 50MG
ARRY-162 is a potent, orally bioavailable and non-ATP competitive inhibitor of MEK1/2 (IC50 = 12 nM ) and cellular pERK (IC50 = 11 nM), selective against a panel of other 220 kinases (has no activity at 10 uM). It shows ex vivo inhibition of cytokine production such as IL-1, TNF and IL-6. It is currently in clinical trials.
Apexbio Technology LLC Robenidine hydrochloride 25875-50-7 100mg
Robenidine hydrochloride (CAS 25875-50-7) is a small-molecule antimicrobial agent with activity against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) It is designed to inhibit these bacterial pathogens thereby interfering with microbial survival Robenidine hydrochloride exerts its biological activity primarily through disruption of microbial cell membrane integrity In in vitro studies Robenidine hydrochloride demonstrates inhibitory activity with MIC50 values of 8 1 M for MRSA and 4 7 M for VRE Based on these pharmacological properties Robenidine hydrochloride holds research potential in the fields of microbial infection drug resistance and the development of novel anti-infective strategies
Medchemexpress LLC Amoxicillin impurity 6 | 205826-86-4 | MFCD24682763 | 50mg
Amoxicillin Impurity 6 is an impurity of Amoxicillin (HY-B0467A)
Medchemexpress LLC Rebamipide impurity 6 | 90098-08-1 | 100mg
Rebamipide impurity 6 is an impurity of Rebamipide (HY-B0360)
Indofine Chemical Psoralen With Hplc, 10 Mg
PSORALEN with HPLC 10 MG, Coumarin, Ficusin, C11H6O3, MW: 186.16, 98% by HPLC, 66-97-7, MFCD00010520
![Medchemexpress LLC (E)-N-[4-(3-chloro-4-(3-fluorophenyl)methoxy)anilino]-4-(dimethylamino)but-2-enamide | 848133-17-5 | MFCD26792555 | >98.0% | 574.0 g/mol | C31H29ClFN5O3 | 10 MM 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000246335.png-250.jpg)
Medchemexpress LLC (E)-N-[4-(3-chloro-4-(3-fluorophenyl)methoxy)anilino]-4-(dimethylamino)but-2-enamide | 848133-17-5 | MFCD26792555 | >98.0% | 574.0 g/mol | C31H29ClFN5O3 | 10 MM 1 ML
HKI-357 is an irreversible small-molecule inhibitor of EGFR and ERBB2 used as a research reagent to probe receptor autophosphorylation and downstream signaling pathways. It shows potent cellular activity (reported IC50s ~34 nM and 33 nM) and is provided as a solid or as a ready-to-use DMSO solution for cell signaling studies.
- Irreversible dual inhibitor of EGFR and ERBB2.
- Potent activity with IC50s around 34 nM and 33 nM.
- Suppresses EGFR autophosphorylation (Y1068) and downstream AKT and MAPK signaling.
- Available as 10 mM solution in DMSO or as solid quantities for flexible dosing.
- High purity, typically ≥98% (HPLC), suitable for research applications.
Medchemexpress LLC Pantoprazole sodium hydrate | 164579-32-2 | 99.93% | 432.37 | 250 MG
Pantoprazole sodium hydrate is an orally active and potent proton pump inhibitor (PPI) and a substituted benzimidazole. It is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. It improves pH stability and possesses anti-secretory and anti-ulcer activities. It also significantly increased tumor growth delay when combined with Doxorubicin.
- Orally active and potent proton pump inhibitor
- Substituted benzimidazole
- Potent H+/K-ATPase inhibitor with an IC50 of 6.8 μM
- Improves pH stability
- Anti-secretory and anti-ulcer activities
- Increases tumor growth delay in combination with Doxorubicin
Sigma Aldrich Fine Chemicals Biosciences Palonosetron Related Compound E United States Pharmacopeia (USP) Reference Standard | 135729-55-4 | 15MG
Palonosetron Related Compound E United States Pharmacopeia (USP) Reference Standard | Mol Wt: 330.85 | 135729-55-4 | 15MG
![Medchemexpress LLC Phosphonic acid, P-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl] hydrate | 206184-49-8 | MFCD11519982 | 99.5% | C10H16N5O4P·H2O | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260772.png-250.jpg)
Medchemexpress LLC Phosphonic acid, P-[[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl] hydrate | 206184-49-8 | MFCD11519982 | 99.5% | C10H16N5O4P·H2O | 10MG
Tenofovir hydrate is an antiviral nucleotide reverse transcriptase inhibitor provided for research use. It is used in studies of HIV and chronic hepatitis B and is supplied as a high-purity white to off-white powder suitable for biochemical and cell-based assays. This product is intended for laboratory research and not for clinical use.
- High purity suitable for research applications.
- White to off-white powder, easy to weigh and dissolve.
- Available as solid, solution in DMSO, or pre-dissolved formats.
- Suitable for biochemical and cell-based antiviral assays.
- Batch-specific certificate of analysis available for validation.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC Dabigatran impurity 2 | 1580491-16-2 | 10mg
Dabigatran impurity 2 is an impurity of Dabigatran (HY-10163)