Sulfanilides
![eMolecules Medchem Express / (R)-BAY-899 / 5mg / 673358877 / HY-130248B / / / [null] / 459.457 / C25H19F2N5O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502456876.PNG-250.jpg)
eMolecules Medchem Express / (R)-BAY-899 / 5mg / 673358877 / HY-130248B / / / [null] / 459.457 / C25H19F2N5O2
Medchem Express / (R)-BAY-899 / 5mg / 673358877 / HY-130248B / / / [null] / 459.457 / C25H19F2N5O2
Accela Chembio Inc N | n-bis(trifluoromethanesulfonyl)aniline | 25g | 37595-74-7 | MFCD00000404 | 98% | Shelf Life: 1800 Days | Light Sensitive/moisture Sensitive
N | n-bis(trifluoromethanesulfonyl)aniline | 25g | 37595-74-7 | MFCD00000404 | 98% | Shelf Life: 1800 Days | Light Sensitive/moisture Sensitive
Medchemexpress LLC Abrocitinib | 1622902-68-4 | MFCD30187577 | 99.3% | 323.41 g·mol⁻¹ | C14H21N5O2S | 25 MG
Abrocitinib is a potent, orally active, and selective Janus kinase 1 (JAK1) inhibitor used in preclinical pharmacology. It shows strong JAK1 inhibition (reported IC50 ≈ 29 nM) with reduced activity against JAK2 and TYK2, and is used in in vitro and in vivo models of autoimmune and inflammatory disease.
- Potent and selective JAK1 inhibition.
- Demonstrated cellular activity inhibiting STAT phosphorylation.
- High purity for reproducible experimental results.
- Available as solid and as DMSO solution for flexible dosing.
- Multiple in vivo formulation protocols provided for administration.
- Recommended storage conditions support long-term stability.
Medchemexpress LLC HY-15251 5mg Medchemexpress, Reparixin CAS:266359-83-5 Purity:>98%
Medchemexpress, HY-15251 5mg Reparixin CAS:266359-83-5 Reparixin is a non-competitive allosteric inhibitor of the chemokine receptors CXCR1 and CXCR2 activation with IC50s of 1 and 100 nM, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Selleck Chemical LLC AZ876
AZ876 is a novel high-affinity Liver X Receptor (LXR) agonist with Ki values of 0 007 M and 0 011 M for human LXR and LXR respectively
Medchemexpress LLC HY-12289 10mg Medchemexpress, Defactinib CAS:1073154-85-4 Purity:>98%
Medchemexpress, HY-12289 10mg Defactinib CAS:1073154-85-4 Defactinib (VS-6063; PF-04554878) is a novel FAK inhibitor with potential antiangiogenic and antineoplastic activities. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-15466 5mg Medchemexpress, CH5132799 CAS:1007207-67-1 Purity:>98%
Medchemexpress, HY-15466 5mg CH5132799 CAS:1007207-67-1 CH5132799 is a selective class I PI3K inhibitor. CH5132799 inhibits class I PI3Ks, particularly PI3Kα, with an IC50 of 14 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-112279 10mg Medchemexpress, GNE-131 CAS:1629063-81-5 Purity:>98%
Medchemexpress, HY-112279 10mg GNE-131 CAS:1629063-81-5 GNE-131 is a potent and selective inhibitor of human sodium channel NaV1.7, with an IC50 of 3 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-108677 10mg Medchemexpress, L-368,899 hydrochloride CAS:160312-62-9 Purity:>98%
Medchemexpress, HY-108677 10mg L-368,899 HCl CAS:160312-62-9 L-368,899 hydrochloride is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist, with IC50s of 8.9 nM and 26 nM for rat uterus and human uterus oxytocin receptor, respectively, used as a tocolytic agent. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-10934 5mg Medchemexpress, Mibampator CAS:375345-95-2 Purity:>98%
Medchemexpress, HY-10934 5mg Mibampator CAS:375345-95-2 Mibampator (LY451395) is a potent and highly selective potentiator of the AMPA receptors. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
eMolecules S 3304 | 203640-27-1 | MFCD22200275 | 50mg
Ambeed | S 3304 | 50mg | 525023885 | A123766 | | 203640-27-1 | MFCD22200275 | 464.550 | C24H20N2O4S2
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Medchemexpress LLC (R)-Bay-899 | 2988191-40-6 | 99.9% | C25H19F2N5O2 | 10MG
(R)-BAY-899 is the R-enantiomer of an orally active, selective luteinizing hormone receptor (LH-R) antagonist supplied for research use. Provided as an off-white to light yellow solid with high reported purity and defined molecular properties, it is intended for biochemical and pharmacological studies including receptor pharmacology and in vitro assays.
- High purity: 99.9%.
- Molecular formula: C25H19F2N5O2.
- Molecular weight: 459.45 g/mol.
- CAS registry number: 2988191-40-6.
- Off-white to light yellow solid appearance.
- Reported activity against LH receptor with IC50s of 185 nM (human) and 46 nM (rat).
- For research use only; not for human therapeutic use.