Pyrroles
Medchemexpress LLC HY-109020 5mg Medchemexpress, Acrizanib CAS:1229453-99-9 Purity:>98%
Medchemexpress, HY-109020 5mg Acrizanib CAS:1229453-99-9 Acrizanib is a VEGFR-2 inhibitor, with an IC 50 of 17.4 nM for BaF3-KDR. 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-111754 5mg Medchemexpress, DMX-5804 CAS:2306178-56-1 Purity:>98%
Medchemexpress, HY-111754 5mg DMX-5804 CAS:2306178-56-1 DMX-5804 is a potent, orally active and selective MAP4K4 inhibitor, with an IC 50 of 3 nM, a pIC 50 of 8.55 for human MAP4K4, less potent on MINK1/MAP4K6 ( pIC 50 , 8.18), and TNIK/MAP4K7 ( pIC 50 , 7.96). DMX-5804 enhances cardiomyocyte survival, and reduces ischemia-reperfusion injury in mice [1] . 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-112706 5mg Medchemexpress, PF-06747711 CAS:1892576-58-7 Purity:>98%
Medchemexpress, HY-112706 5mg PF-06747711 CAS:1892576-58-7 PF-06747711 is a potent, selective, and orally active retinoic acid receptor-related orphan C2 ( RORC2 , also known as RORγt ) inverse agonist, with an IC 50 of 4.1 nM. Anti-skin inflammatory activity [1] . 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-15816A 5mg Medchemexpress, Ulixertinib (hydrochloride) CAS:1956366-10-1 Purity:>98%
Medchemexpress, HY-15816A 5mg Ulixertinib (hydrochloride) CAS:1956366-10-1 Ulixertinib hydrochloride is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC 50 of <0.3 nM against ERK2. Ulixertinib hydrochloride inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line [1] [2] . 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-18971 5mg Medchemexpress, TG4-155 CAS:1164462-05-8 Purity:>98%
Medchemexpress, HY-18971 5mg TG4-155 CAS:1164462-05-8 TG4-155 is a potent, brain-permeant and selective EP2 receptor antagonist with a K i of 9.9 nM [1] [2] . TG4-155 shows low nanomolar antagonist activity against only EP2 and DP1 [1] . TG4-155 has an EP2 Schild K B of 2.4 nM and displays 550-4750-fold selectivity for EP2 over EP1, EP3, EP4 and IP, but only 14-fold selectivity against the DP1 receptor [2] . 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-B0002B 50mg Medchemexpress, Ondansetron CAS:99614-02-5 Purity:>98%
Medchemexpress, HY-B0002B 50mg Ondansetron CAS:99614-02-5 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.
Sigma Aldrich Fine Chemicals Biosciences Metergoline | 17692-51-2 | MFCD00153829 | 5G
Metergoline | Mol Wt: 403.52 | 17692-51-2 | MFCD00153829 | 5G
Sigma Aldrich Fine Chemicals Biosciences Ondansetron for TLC system suitability European Pharmacopoeia (EP) Reference Standard | 103639-04-9 | MFCD00374371 |
Ondansetron for TLC system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 365.85 | 103639-04-9 | MFCD00374371 |
Sigma Aldrich Fine Chemicals Biosciences IU1 >=98% (HPLC) | 314245-33-5 | MFCD01917473 | 25MG
IU1 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 300.37 | 314245-33-5 | MFCD01917473 | 25MG
AG Scientific Inc Staurosporine 5 MG
Staurosporine is a cell-permeable protein kinase inhibitor that acts by blocking interaction with the ATP binding site. It mainly inhibits protein kinase C (PKC) but most other kinases, including tyrosine kinases. It has some antifungal properties.It has been reported that Staurosporine promotes apoptosis in various cell types by triggering both the morphological changes and intranucleosomal DNA fragmentation and by caspase-dependent and -independent ways. In addition, it has been reported that the kinase inhibitor is related to signaling pathway.
eMolecules Medchem Express / MI-538 / 1mg / 446270404 / HY-19810 / / 1857417-10-7 / MFCD30532690 / 566.610 / C27H25F3N8OS
Medchem Express / MI-538 / 1mg / 446270404 / HY-19810 / / 1857417-10-7 / MFCD30532690 / 566.610 / C27H25F3N8OS
eMolecules Medchem Express / AZ PFKFB3 26 / 5mg / 482203815 / HY-101971 / / 1704740-52-2 / MFCD30742931 / 402.498 / C24H26N4O2
Medchem Express / AZ PFKFB3 26 / 5mg / 482203815 / HY-101971 / / 1704740-52-2 / MFCD30742931 / 402.498 / C24H26N4O2
eMolecules Medchem Express / iCRT 14 / 5mg / 446267627 / HY-16665 / / 677331-12-3 / MFCD04366833 / 375.450 / C21H17N3O2S
Medchem Express / iCRT 14 / 5mg / 446267627 / HY-16665 / / 677331-12-3 / MFCD04366833 / 375.450 / C21H17N3O2S
![eMolecules Medchem Express / JNJ-63576253 / 5mg / 589794133 / HY-115282A / / 2110428-64-1 / [null] / 538.970 / C23H22ClF3N6O2S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502449974.PNG-250.jpg)
eMolecules Medchem Express / JNJ-63576253 / 5mg / 589794133 / HY-115282A / / 2110428-64-1 / [null] / 538.970 / C23H22ClF3N6O2S
Medchem Express / JNJ-63576253 / 5mg / 589794133 / HY-115282A / / 2110428-64-1 / [null] / 538.970 / C23H22ClF3N6O2S