Pyrroles
eMolecules (S)-2-N-BOC-AMINO-1-PYRROLIDIN-1-YL-PROPAN-1-ONE | 138356-92-0 | MFCD09025328 | 1g
AstaTech | (S)-2-N-BOC-AMINO-1-PYRROLIDIN-1-YL-PROPAN-1-ONE | 1g | 112523971 | 55920 | 97.000 | 138356-92-0 | MFCD09025328 | 242.319 | C12H22N2O3
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eMolecules Building Block Tool
![eMolecules Medchem Express / TLR7/8 agonist 4 / 5mg / 779534659 / HY-139017 / / 2388520-33-8 / [null] / 324.432 / C18H24N6](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502473513.JPG-250.jpg)
eMolecules Medchem Express / TLR7/8 agonist 4 / 5mg / 779534659 / HY-139017 / / 2388520-33-8 / [null] / 324.432 / C18H24N6
Medchem Express / TLR7/8 agonist 4 / 5mg / 779534659 / HY-139017 / / 2388520-33-8 / [null] / 324.432 / C18H24N6
eMolecules Medchem Express / PBOX 6 / 5mg / 446276101 / HY-U00446 / / 290814-68-5 / MFCD31382391 / 396.446 / C25H20N2O3
Medchem Express / PBOX 6 / 5mg / 446276101 / HY-U00446 / / 290814-68-5 / MFCD31382391 / 396.446 / C25H20N2O3
Apexbio Technology LLC Sunitinib 557795-19-4 10mM (in 1mL DMSO)
Sunitinib (CAS 557795-19-4) is an orally bioavailable small molecule inhibitor targeting multiple receptor tyrosine kinases (RTKs) including VEGFR1-3 PDGFR / c-kit and RET Research has shown sunitinib inhibits proliferation in nasopharyngeal carcinoma (NPC) cell lines HK1 CNE-1 CNE-2 HONE-1 and C666-1 with IC50 values ranging from approximately 2 06 to 7 57 M Additionally it induces apoptosis and G0/G1 cell cycle arrest in NPC cell lines and significantly decreases microvessel density in CNE-2 xenograft tumor models in vivo Thus sunitinib is useful for investigating pathways involved in tumor angiogenesis and proliferation
eMolecules AstaTech / 4-DIFLUOROMETHOXY-3-FLUOROPHENYLACETIC ACID / 1g / 164730171 / CL8923 / 95.000 / 1261851-55-1 / MFCD18395038 / 220.147 / C9H7F3O3
AstaTech / 4-DIFLUOROMETHOXY-3-FLUOROPHENYLACETIC ACID / 1g / 164730171 / CL8923 / 95.000 / 1261851-55-1 / MFCD18395038 / 220.147 / C9H7F3O3
eMolecules Medchem Express / BQ-788 / 1mg / 415687676 / HY-15894A / / 173326-37-9 / MFCD06245594 / 641.810 / C34H51N5O7
Medchem Express / BQ-788 / 1mg / 415687676 / HY-15894A / / 173326-37-9 / MFCD06245594 / 641.810 / C34H51N5O7
Medchemexpress LLC Az PFKFB3 26 | 1704740-52-2 | MFCD30742931 | 98.3% | 402.49 | C24H26N4O2 | 25 MG
AZ PFKFB3 26 is a potent, selective small-molecule inhibitor of PFKFB3 used in research on glycolytic regulation and cancer metabolism. It displays low-nanomolar biochemical potency and measurable cellular effects in tumor cell assays, and is provided as a high-purity solid for laboratory use.
- Potent PFKFB3 biochemical inhibitor (IC50 23 nM).
- Selective over PFKFB1 and PFKFB2 (IC50s 2.06 μM and 0.384 μM).
- Active in A549 cells (fructose-1,6-bisphosphate reduction IC50 0.343 μM).
- High-purity research-grade material suitable for in vitro studies.
- Available in small pack sizes for preclinical experiments.
Medchemexpress LLC PHA-767491 hydrochloride | 942425-68-5 | MFCD11519962 | 99.5% | 249.70 | C12H12ClN3O | 5 MG
PHA-767491 hydrochloride is a small-molecule research inhibitor that selectively targets Cdc7 and Cdk9 kinases. It is used in biochemical and cellular studies to probe DNA replication initiation, transcriptional regulation, and cancer cell proliferation. The compound exhibits low-nanomolar biochemical potency and measurable cellular activity, and is supplied as a high-purity solid for laboratory research.
- Potent dual Cdc7/Cdk9 inhibition with low-nanomolar IC50 values.
- Demonstrated cellular antiproliferative activity in multiple cancer cell lines.
- High purity suitable for biochemical and cellular assays.
- Solid, light yellow to yellow appearance for convenient handling.
- Stable under recommended storage conditions for research use.
- Analytical documentation available, including datasheet, COA, and SDS.
eMolecules AstaTech / 2-AMINO-3-BROMO-4-FLUOROPHENOL / 0.1g / 717406234 / E86451 / 95.000 / 1805533-08-7 / MFCD28738821 / 206.014 / C6H5BrFNO
AstaTech / 2-AMINO-3-BROMO-4-FLUOROPHENOL / 0.1g / 717406234 / E86451 / 95.000 / 1805533-08-7 / MFCD28738821 / 206.014 / C6H5BrFNO
Medchemexpress LLC HY-79077 5mg Medchemexpress, Osimertinib (dimesylate) CAS:2070014-82-1 Purity:>98%
Medchemexpress, HY-79077 5mg Osimertinib (dimesylate) CAS:2070014-82-1 Osimertinib dimesylate (AZD-9291 dimesylate) is an irreversible and mutant selective EGFR inhibitor with IC50s of 12 and 1 nM against EGFRL858R and EGFRL858R/T790M, 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.
Medchemexpress LLC HY-19511 5mg Medchemexpress, GSK2018682 CAS:1034688-30-6 Purity:>98%
Medchemexpress, HY-19511 5mg GSK2018682 CAS:1034688-30-6 GSK2018682 is an agonist for S1P1 and S1P5 receptor with pEC50s of 7.7 and 7.2, respectively, and has no agonist activity towards human S1P2, S1P3, or S1P4. GSK2018682 is used in the research of multiple sclerosis. 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 Target Molecule Sunitinib Malate 500mg 376013295 T0374 0 000 341031-54-7 MFCD08282795 532 569 C26H33FN4O7
Target Molecule Sunitinib Malate 500mg 376013295 T0374 0 000 341031-54-7 MFCD08282795 532 569 C26H33FN4O7
Med Vet International Atorvastatin 20mg, 90 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Atorvastatin 20mg, 90 tablets