Sulfanilides
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-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-12289A 5mg Medchemexpress, Defactinib (hydrochloride) CAS:1073160-26-5 Purity:>98%
Medchemexpress, HY-12289A 5mg Defactinib (hydrochloride) CAS:1073160-26-5 Defactinib hydrochloride (VS-6063 hydrochloride; PF 04554878 hydrochloride) is a novel FAK inhibitor, which inhibits FAK phosphorylation at the Tyr397 site in a time- and dose-dependent manner. 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-13421 5mg Medchemexpress, SR1001 CAS:1335106-03-0 Purity:>98%
Medchemexpress, HY-13421 5mg SR1001 CAS:1335106-03-0 SR1001 is a selective RORα and RORγt inverse agonist with Kis 172 and 111 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 O-3M3FBS | 313981-55-4 | 343.36 | 10 MG
o-3M3FBS acts as the negative control for m-3M3FBS. It inhibits inward and outward currents through mechanisms independent of PLC, functioning antagonistically. Additionally, it causes an increase in [Ca2+]i in an agonistic manner.
- Inhibits inward and outward currents independently of PLC
- Acts antagonistically to certain mechanisms
- Increases [Ca2+]i agonistically
- Target: Calcium Channel
- Pathway: Membrane Transporter/Ion Channel; Neuronal Signaling
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.
eMolecules 1033906-44-3 | 3,3,3-Trifluoropropane sulfonamide | Oakwood Chemicals | MFCD08704575 | 177.140 | C3H6F3NO2S | 98.000 | NS(=O)(=O)CCC(F)(F)F | 25g | 480131332
3,3,3-Trifluoropropane sulfonamide | Oakwood Chemicals | 1033906-44-3 | MFCD08704575 | 177.140 | C3H6F3NO2S | 98.000 | NS(=O)(=O)CCC(F)(F)F | 25g | 480131332
eMolecules (2E)-3-(2,5-Dimethoxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one | 151135-94-3 | | 100mg
Oakwood Chemical | (2E)-3-(2,5-Dimethoxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one | 100mg | 537713722 | 191039 | | 151135-94-3 | | 284.311 | C17H16O4
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Medchemexpress LLC Dpm-1001 | 1471172-27-6 | 99.8% | 10 MG
DPM-1001 is a potent, orally active, and non-competitive inhibitor of protein-tyrosine phosphatase 1B (PTP1B) that shows in vitro activity (IC50 ≈ 100 nM) and in vivo efficacy in diet-induced obese mice.
- Potent PTP1B inhibition with IC50 around 100 nM
- Orally active and non-competitive mechanism of action
- Demonstrated efficacy in animal models improving glucose tolerance and reducing body weight
- High reported purity suitable for research use
- Available in small pack sizes for preclinical studies
Medchemexpress LLC Bay-899 | 2471967-92-5 | 99.9% | C25H19F2N5O2 | 10MG
BAY-899 is a tetrahydro-1,6-naphthyridine-based small-molecule antagonist of the luteinizing hormone receptor (LH-R), used as a research probe to modulate LH-R signaling and reduce sex hormone levels in vitro and in vivo.
- Orally active small molecule with demonstrated in vivo activity.
- Selective LH-R antagonism with IC50s: human 185 nM, rat 46 nM.
- High chemical purity (99.9%) suitable for biochemical assays.
- Molecular formula C25H19F2N5O2; molecular weight 459.45 g·mol⁻¹.
- Supplied as a solid for solution preparation and dosing studies.
Medchemexpress LLC HY-14870 50mg , NS-304 Selexipag;ACT-293987 CAS:475086-01-2 Purity:98%
Medchemexpress, HY-14870 50mg NS-304 Selexipag;ACT-293987 CAS:475086-01-2 Formula:C26H32N4O4S Prostacyclin receptor Purity:98% NS-304 is an orally available and potent agonist for the Prostacyclin ( PGI 2 ) receptor (IP receptor). 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.
Advanced Chemblocks Inc 1,1,1-Trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide; 50G; 95%
Chemical Name: 1,1,1-Trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide CAS: 37595-74-7 MW: 357.25 MDL Number: MFCD00000404 Synonym: 1,1,1-Trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide
Medchemexpress LLC HY-103007 5mg Medchemexpress, TC-G-1008 CAS:1621175-65-2 Purity:>98%
Medchemexpress, HY-103007 5mg TC-G-1008 CAS:1621175-65-2 TC-G-1008 (GPR39-C3) is a potent and orally available GPR39 agonist with EC50 values of 0.4 and 0.8 nM for rat and human receptors 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.