Chromatography Standards
Medchemexpress LLC Lenalidomide-4-aminomethyl hydrochloride | 444289-05-8 | 90.9% | 309.75 | 100 MG
Lenalidomide-4-aminomethyl hydrochloride is a lenalidomide-based cereblon (CRBN) ligand utilized for the recruitment of CRBN protein. It can be linked to a ligand for protein via a linker to form PROTAC.
- Lenalidomide-based cereblon (CRBN) ligand
- Used in the recruitment of CRBN protein
- Can be connected to a ligand for protein by a linker to form PROTAC
Sigma Aldrich Fine Chemicals Biosciences Domperidone maleate European Pharmacopoeia (EP) Reference Standard | 83898-65-1 |
Domperidone maleate European Pharmacopoeia (EP) Reference Standard | Mol Wt: 541.98 | 83898-65-1 |
Sigma Aldrich Fine Chemicals Biosciences Sulbactam Related Compound D United States Pharmacopeia (USP) Reference Standard | 4027-64-9 | 15MG
Sulbactam Related Compound D United States Pharmacopeia (USP) Reference Standard | Mol Wt: 318.23 | 4027-64-9 | 15MG
![Medchemexpress LLC N-(4-((3-chloro-4-fluorophenyl)amino)pyrido[3,4-d]pyrimidin-6-yl)-N'-(1-(dimethylamino)propan-2-yl)a | 848133-17-5 | MFCD26792555 | 99.2% | 574.05 | C31H29ClFN5O3 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000245116.png-250.jpg)
Medchemexpress LLC N-(4-((3-chloro-4-fluorophenyl)amino)pyrido[3,4-d]pyrimidin-6-yl)-N'-(1-(dimethylamino)propan-2-yl)a | 848133-17-5 | MFCD26792555 | 99.2% | 574.05 | C31H29ClFN5O3 | 5 MG
HKI-357 is an irreversible small-molecule inhibitor of EGFR and ERBB2 kinases. It inhibits EGFR autophosphorylation at Y1068 and reduces downstream AKT and MAPK phosphorylation, showing potent activity in cell signaling and preclinical cancer models. Supplied as a solid research reagent for in vitro and preclinical studies.
- Irreversible dual inhibitor of EGFR and ERBB2
- Potent activity: EGFR 34 nM, ERBB2 33 nM
- Suppresses EGFR Y1068 autophosphorylation and downstream signaling
- Supplied as a solid, >99% purity (batch-dependent)
- Suitable for kinase signaling and preclinical cancer research
Med Vet International 2% Diclofenac Sodium, Topical Solution, 112gm, Each
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
2% Diclofenac Sodium, Topical Solution, 112gm, Each
Medchemexpress LLC Acarbose | 56180-94-0 | 99.97% | C25H43NO18 | 10 MM/1 ML
Acarbose is an orally active alpha-glucosidase inhibitor and an antihyperglycemic agent. It works by slowing the digestion and absorption of complex carbohydrates, thereby leading to a more gradual rise in blood glucose levels after meals. Primarily used in the management of type 2 diabetes mellitus, it can potentiate the hypoglycemic effects of sulfonylureas or insulin.
- Antihyperglycemic agent
- Orally active alpha-glucosidase inhibitor (IC50=11 nM)
- Potentiates hypoglycemic effects of sulfonylureas or insulin
- Slows digestion and absorption of carbohydrates
- Used for management of type 2 diabetes mellitus
- Available as a solid, white to light yellow powder
- Soluble in water
Sigma Aldrich Fine Chemicals Biosciences Econazole Related Compound5MG
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
Medchemexpress LLC Atovaquone | 95233-18-4 | 99.75% | 366.84 | 50 MG
Atovaquone is a potent, selective, and orally active inhibitor targeting the parasite's mitochondrial cytochrome bc1 complex. It is effective against human and *P. falciparum* cytochrome bc1 activity and is recognized as an antimalarial agent.
- Potent, selective, and orally active inhibitor of the parasite's mitochondrial cytochrome bc1 complex
- Effective against human and *P. falciparum* cytochrome bc1 activity
- Functions as an antimalarial agent
- Potential for investigation of pneumocystis pneumonia, toxoplasmosis, malaria, and babesia
- Targets the Qo site of the *Plasmodium* cytochrome bc1 complex within the mitochondrial electron transport chain
- Demonstrates transmission blocking potential against mosquito development
Sigma Aldrich Fine Chemicals Biosciences Aripiprazole Related Compound F United States Pharmacopeia (USP) Reference Standard | 573691-09-5 | 25MG
Aripiprazole Related Compound F United States Pharmacopeia (USP) Reference Standard | Mol Wt: 464.38 | 573691-09-5 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Deflazacort United States Pharmacopeia (USP) Reference Standard | 14484-47-0 | MFCD00866106 | 100MG
Deflazacort United States Pharmacopeia (USP) Reference Standard | Mol Wt: 441.52 | 14484-47-0 | MFCD00866106 | 100MG
Cayman Chemical Fenofibrate, Purity: ≥98%, CAS: 49562-28-9, 5 g
A PPARα agonist (EC50s = 18 and 30 μM for mouse and human receptors, respectively, in a transactivation assay); selective for PPARα over PPARγ (EC50s = 300 and 200 μM for mouse and human receptors, respectively) and lacks activity at mouse and human PPARδ at 100 μM; reduces plasma levels of triglycerides, C-reactive protein, and MDA in mice with fructose-induced hypertriglycemia from 50-100 mg/kg; decreases cisplatin-induced glomerular and tubular atrophy and necrosis in rat kidney at 100 mg/kg; reduces the number of 4-NQO-induced pulmonary lesions in lung in TSOD mice
Cayman Chemical Mirabegron Impurity 6, Purity: ≥95%, CAS: 391901-45-4, 100 mg
A metabolite of mirabegron; formed via hydrolysis of mirabegron by BChE; an intermediate in the synthesis of mirabegron
Enzo Life Sciences Busulfan (10g). CAS: 55-98-1
Antineoplastic bifunctional, DNA alkylating agent that causes DNA damage by cross-linking DNA and proteins. Causes double-base lesions mainly at 5’-GA-3’ and, to a lesser extent, at 5’-GG-3’ sequences. Forms an intrastrand cross-link at the 5’-GA-3’ sequence, in addition to monoalkylation. Selectively induces normal human fibroblast senescence through Erk and p38 pathways. Alternative name: 1,4-Butanediol dimethanesulfonate. Purity: ≥98% (Assay). Solubility: Soluble in acetone, 100% ethanol or DMSO; insoluble in water. Long Term Storage: -20°C.
Sigma Aldrich Fine Chemicals Biosciences Sulbactam European Pharmacopoeia (EP) Reference Standard | 68373-14-8 | MFCD00867005 |
Sulbactam European Pharmacopoeia (EP) Reference Standard | Mol Wt: 233.24 | 68373-14-8 | MFCD00867005 |