Sugar acids and derivatives
Medchemexpress LLC Prosaikogenin D | 103629-72-7 | 10 MG
Prosaikogenin D is isolated from the roots of Buleurum bicaule Helm (Apiaceae) and exhibits anti-cancer activity.
- Suppresses the proliferation of A549 cells with an IC50 of 57.2 μg/mL.
Medchemexpress LLC Integrin alpha 5 bet 50ug | 50ug
ITGA5 is a multifunctional receptor that interacts with multiple ligands such as fibronectin fibrinogen PLA2G2A fibrillin-1 (FBN1) IL1B human metapneumovirus and soluble CD40LG ITGA5 recognizes RGD sequences and mediates cell adhesion through different binding sites Integrin alpha 5 beta 1 Protein Human (HEK293 His-Avi) is a recombinant protein dimer complex containing human-derived Integrin alpha 5 beta 1 protein expressed by HEK293 with C-Avi C-His labeled tag Integrin alpha 5 beta 1 Protein Human (HEK293 His-Avi) has molecular weight of 100-140 kDa
Medchemexpress LLC IL-1RA/IL-1F3 Porci 500ug | 500ug
IL-1RA/IL-1F3 proteins are powerful anti-inflammatory antagonists in the interleukin 1 family specifically targeting the pro-inflammatory cytokines IL1B and IL1A This protein counteracts the inflammatory effects of IL1 playing a critical role in preventing immune dysregulation and preventing uncontrolled systemic inflammation triggered by a variety of innate irritants including pathogens IL-1RA/IL-1F3 Protein Porcine is the recombinant Porcine-derived IL-1RA/IL-1F3 protein expressed by E coli with tag free
Medchemexpress LLC 1-Acetylpiperazine-d4 | 1398065-90-1 | 132.20 | 25MG
1-Acetylpiperazine-d4 is a deuterium-labeled form of 1-Acetylpiperazine. Stable heavy isotopes of hydrogen, carbon, and other elements are incorporated into drug molecules, primarily as tracers for quantitation in drug development. Deuteration has the potential to influence the pharmacokinetic and metabolic profiles of drugs.
- Deuterium labeled compound
- Suitable as a tracer for quantitation in drug development
- Potential to impact pharmacokinetic and metabolic profiles
- For research use only
Apexbio Technology LLC Beta-Lipotropin (1-10), porcine 77875-68-4 25mg
Beta-Lipotropin 1-10 porcine is an endogenous opioid peptide fragment derived from the N-terminal region of beta-lipotropin It is structurally related to opioid peptides and interacts with opioid receptors to mediate morphine-like activity within the central nervous system Beta-Lipotropin 1-10 porcine exerts its biological effects through modulation of opioid receptor signaling pathways Based on these pharmacological properties Beta-Lipotropin 1-10 porcine holds research potential in neuropharmacological studies particularly in investigations related to endogenous pain modulation neurotransmission mechanisms and opioid receptor ligand interactions
Medchemexpress LLC Integrin alpha V bet 5ug
Integrin V beta 3 proteins specifically the -V (ITGAV) subunit are multifunctional receptors for ligands such as vitronectin and fibronectin and recognize RGD sequences ITGAV ITGB3 binds fractalkine and acts as a coreceptor in CX3CR1-dependent signaling Integrin alpha V beta 3 Protein Human (HEK293 C-His) is a recombinant protein dimer complex containing human-derived Integrin alpha V beta 3 protein expressed by HEK293 with C-10 His labeled tag Integrin alpha V beta 3 Protein Human (HEK293 C-His) has molecular weight of 90 31 110-150 kDa respectively
Medchemexpress LLC Cdk1/Cyc B-IN-1 | 2459916-56-2 | 98.5% | 353.85 | 5 MG
CDK1/Cyc B-IN-1 is a selective inhibitor of the CDK1/Cyc B complex, exhibiting an IC50 of 97 nM. This compound induces apoptosis and G2/M cell cycle arrest. It demonstrates broad-spectrum cytotoxic activity across various cancer cell lines.
- Selective CDK1/Cyc B complex inhibitor.
- IC50 of 97 nM against CDK1-Cyclin B.
- Triggers apoptosis.
- Induces G2/M cell cycle arrest.
- Exhibits broad-spectrum cytotoxic action against cancer cell lines.
- Shows cytotoxic activity against HCT-116 and WI-38 cells with IC50 values of 5.33 ± 0.69 μM and 21.69 ± 1.04 μM respectively.
Medchemexpress LLC Protac BET-binding moiety 2 | 916493-82-8 | 99.8% | 10 MG
Small-molecule BET bromodomain inhibitor intended as the BET-binding ligand component in PROTAC constructs and for biochemical and cell-based research applications. Supplied as a solid or as a 10 mM solution in DMSO, with reported high purity and identifying registry information for compound verification.
- Functions as a BET bromodomain ligand for PROTAC design and target engagement studies.
- Available as solid powder and as a 10 mM solution in DMSO for assay flexibility.
- High reported purity suitable for research use.
- Characterized by CAS 916493-82-8 and molecular weight 444.89 for identification.
- Provided for research use only; not for human or clinical use.
Cayman Chemical D-GlucuronIc AcId 10g
A metabolite of glucose; a component of proteoglycans; levels are increased in fibroblasts isolated from patients with ISSD or Salla disease
