Aminobenzoic acids and derivatives
TARGETMOL CHEMICALS INC SITAXSENTAN 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Sitaxsentan (TBC-11251) is A selective endothelin A (ETA) receptor antagonist. Endothelin is an effective vasoconstrictor. Sitaxsentan blocks the binding of endothelin to its receptors thereby eliminating the harmful effects of endothelin. purity: 99%
Cayman Chemical WIN 55 2122 mesylate
A potent aminoalkylindole CB receptor agonist (Ki = 62.3 and 3.3 nM for human recombinant CB1 and CB2 receptors, respectively); increases extracellular glutamate levels in primary cultures of rat cerebral cortex neurons, displaying a bell-shaped concentration-response curve; induces release of the proinflammatory neuropeptide CGRP from trigeminal ganglion neurons in a calcium-dependent manner (EC50 = 26 µM)
Medchemexpress LLC Camostat mesylate | 59721-29-8 | MFCD00941410 | >98.0% | 494.52 | C21H26N4O8S | 5 MG
Camostat mesylate is an orally active, synthetic serine protease inhibitor supplied as the mesylate salt. It inhibits proteases such as trypsin, prostasin, matriptase, and TMPRSS2, and is used in enzymatic and cell-based studies of protease function and viral entry. CAS: 59721-29-8; molecular weight: 494.52.
- Orally active serine protease inhibitor used in research.
- Inhibits TMPRSS2, useful for viral entry and antiviral studies.
- Suitable for enzyme inhibition and cell-based assays.
- Provided as a mesylate salt for enhanced stability and handling.
- Available in small research quantities for assay development.
Medchemexpress LLC A-286982 1mg | 280749-17-9 | 1MG
A-286982 is a potent and allosteric LFA-1/ICAM-1 interaction inhibitor with IC50s of 44 nM and 35 nM in an LFA-1/ICAM-1 binding and LFA-1-mediated cellular adhesion assay respectively[1 [2
Apexbio Technology LLC Ro 31-8220 Mesylate(Synonyms: Ro 31-8220 Methanesulfonate, Bisindolylmaleimide IX mesylate, Ro-318220 Mesylate), 50mg, CAS: 138489-18-6.
Ro 31-8220 Mesylate (CAS 138489-18-6) is a selective small molecule inhibitor of protein kinase C (PKC) targeting multiple PKC isoforms ( I II and ) with IC50 values ranging from 5 to 27 nM PKC constitutes a family of calcium- and phospholipid-dependent serine/threonine kinases implicated in signaling pathways associated with growth factor responses and malignant transformation Ro 31-8220 modulates downstream targets inhibiting MKP-1 and c-Fos expression while inducing c-Jun and activating Jun N-terminal kinase (JNK) in a PKC-dependent manner It suppresses mitogen-induced IL-2 production and T-cell proliferation suggesting utility in immunological research and affects glucose metabolism via JNK and glycogen synthase activation relevant to metabolic studies
eMolecules Oakwood Chemicals Deferoxamine mesylate 250mg 480154951 103966 0 000 138-14-7 MFCD00058605 656 790 C26H52N6O11S
Oakwood Chemicals Deferoxamine mesylate 250mg 480154951 103966 0 000 138-14-7 MFCD00058605 656 790 C26H52N6O11S
eMolecules Combi-Blocks Inc 2-Amino-4-methoxy-nicotinic acid 250mg 869683111 QJ-5164 95 000 773099-92-6 MFCD06208729 168 152 C7H8N2O3
Combi-Blocks Inc 2-Amino-4-methoxy-nicotinic acid 250mg 869683111 QJ-5164 95 000 773099-92-6 MFCD06208729 168 152 C7H8N2O3
Apexbio Technology LLC 2-Amino-dATP(Synonyms: 2-Amino-2'-deoxyadenosine-5'-triphosphate, 2-Amino-dATP nucleotide), 10ul (100 mM).
2-Amino-dATP is a synthetic small molecule capable of modulating specific signaling cascades via enzymatic activity interference It exerts biological effects by inhibiting intracellular signal transduction pathways thereby influencing processes such as cellular proliferation and apoptosis as demonstrated in vitro Given its precise biological mechanism this compound serves as an important molecular tool in studying signal regulation and disease-related pathways in biomedical research contexts