Piperidines
Medchemexpress LLC HY-13736A 5mg Medchemexpress, Quinagolide (hydrochloride) CAS:94424-50-7 Purity:>98%
Medchemexpress, HY-13736A 5mg Quinagolide (hydrochloride) CAS:94424-50-7 0 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.
TARGETMOL CHEMICALS INC ANAMORELIN HYDROCHLORIDE 25MG
Also available in 1 mg 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. AnaMorelin hydrochloride (RC-1291 hydrochloride) is a novel ghrelin receptor agonist(EC50 0.74 nM in the FLIPR assay). purity: 99%
eMolecules Medchem Express / AZD-3463 / 5mg / 446266125 / HY-15609 / / 1356962-20-3 / MFCD25976759 / 448.960 / C24H25ClN6O
Medchem Express / AZD-3463 / 5mg / 446266125 / HY-15609 / / 1356962-20-3 / MFCD25976759 / 448.960 / C24H25ClN6O
Medchemexpress LLC HY-100388 5mg Medchemexpress, SHP099 CAS:1801747-42-1 Purity:>98%
Medchemexpress, HY-100388 5mg SHP099 CAS:1801747-42-1 SHP099 is a potent, selective, orally available SHP2 inhibitor with an IC 50 of 70 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.
eMolecules Ambeed / (2S3R4R5R)-5-(Acetoxymethyl)tetrahydrofuran-234-triyl triacetate / 5g / 552527542 / A108665 / / 13035-61-5 / MFCD00005358 / 318.278 / C13H18O9
Ambeed / (2S3R4R5R)-5-(Acetoxymethyl)tetrahydrofuran-234-triyl triacetate / 5g / 552527542 / A108665 / / 13035-61-5 / MFCD00005358 / 318.278 / C13H18O9
Medchemexpress LLC HY-112167A 5mg Medchemexpress, GDC-0575 dihydrochloride CAS:1657014-42-0 Purity:>98%
Medchemexpress, HY-112167A 5mg GDC-0575 diHCl CAS:1657014-42-0 GDC-0575 dihydrochloride (ARRY-575 dihydrochloride) is an orally bioavailable CHK1 inhibitor, with an IC50 of 1.2 nM, and has antitumor activity. 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-100039 5mg Medchemexpress, YYA-021 CAS:144217-65-2 Purity:>98%
Medchemexpress, HY-100039 5mg YYA-021 CAS:144217-65-2 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.
Apexbio Technology LLC B-Raf inhibitor 1 dihydrochloride 1191385-19-9 100mg
B-Raf inhibitor 1 dihydrochloride (CAS 1191385-19-9) is a small molecule inhibitor targeting B-Raf kinase including both wild-type and mutant forms such as the V600E variant commonly found in tumor cells As a type IIA inhibitor it binds to the DFG-out conformation of the ATP-binding site on B-Raf The compound demonstrates inhibitory activity against cell proliferation with IC50 values of 0 31 M in A375 cells and 0 72 M in HCT116 cells B-Raf inhibitor 1 also inhibits other tyrosine kinases and in cells expressing wild-type B-Raf can promote activation of the RAF-MEK-ERK signaling pathway through Raf dimerization In preclinical mouse models it has been observed to induce proliferation supporting its use in studies of Raf signaling kinase inhibitor specificity and oncogenic pathway modulation
![eMolecules 1-boc-3-azabicyclo[3.2.1]octane-8-methanol | 637301-16-7 | MFCD22566234 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502157984.JPG-250.jpg)
eMolecules 1-boc-3-azabicyclo[3.2.1]octane-8-methanol | 637301-16-7 | MFCD22566234 | 1g
Pharmablock | 1-boc-3-azabicyclo[3.2.1]octane-8-methanol | 1g | 551134382 | PBN20120314 | | 637301-16-7 | MFCD22566234 | 241.331 | C13H23NO3
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
eMolecules (5R)-5-aminopiperidin-2-one hydrochloride | 1003021-01-9 | MFCD03094720 | 1g
Pharmablock | (5R)-5-aminopiperidin-2-one hydrochloride | 1g | 551116899 | PBLJ2833 | | 1003021-01-9 | MFCD03094720 | 150.610 | C5H11ClN2O
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
Apexbio Technology LLC Vanoxerine dihydrochloride 67469-78-7 10mg
Vanoxerine dihydrochloride is a small-molecule inhibitor targeting the dopamine transporter (DAT1) human ether- -go-go-related gene (hERG Kv11 1) potassium channel cardiac sodium channel (hNaV1 5) and L-type calcium channels (ICa L) It modulates neurotransmitter uptake and cardiac ion channel conductance thereby regulating synaptic dopamine levels and cardiac electrophysiology Vanoxerine dihydrochloride exerts its biological activity primarily through inhibition of dopamine reuptake and blockade of multiple cardiac ion channels It demonstrates antagonist activity at DAT1 (Ki 16 9 nM) potent inhibition of hERG channels (IC50 0 84 nM) and inhibitory effects on hNaV1 5 (IC50 830 nM) and ICa L (IC50 320 nM) Based on these pharmacological properties vanoxerine dihydrochloride holds research potential in cardiac arrhythmia studies
![eMolecules Medchem Express / AR-9281 / 5mg / 475641492 / HY-111151 / / 913548-29-5 / [null] / 319.449 / C18H29N3O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502470535.JPG-250.jpg)
eMolecules Medchem Express / AR-9281 / 5mg / 475641492 / HY-111151 / / 913548-29-5 / [null] / 319.449 / C18H29N3O2
Medchem Express / AR-9281 / 5mg / 475641492 / HY-111151 / / 913548-29-5 / [null] / 319.449 / C18H29N3O2
Apexbio Technology LLC SAR7334 1333210-07-3 2mg
SAR7334 (CAS 1333210-07-3) is a small molecule inhibitor that selectively targets the transient receptor potential cation channel subfamily C member 6 (TRPC6) By inhibiting TRPC6-mediated calcium influx SAR7334 is utilized to investigate TRPC6-related signal transduction pathways in cellular and preclinical studies This compound serves as a valuable tool for elucidating the role of TRPC6 in pathophysiological processes including those related to kidney function and vascular regulation Its application aids in advancing the understanding of TRPC6-associated diseases and potential therapeutic interventions
Medchemexpress LLC Btk inhibitor 2 (BGB-3111 analog) | 1558036-85-3 | MFCD31382019 | 99.6% | 431.49 g/mol | C24H25N5O3 | 25 MG
Btk inhibitor 2 (BGB-3111 analog) is a small-molecule inhibitor of Bruton's tyrosine kinase (BTK) described in patent US 20170224688 A1. It is supplied as a research reagent with reported high purity and is intended for in vitro biochemical and cellular studies.
- Bruton's tyrosine kinase inhibitor for research use only.
- Extracted from patent US 20170224688 A1.
- Cas number 1558036-85-3.
- Molecular formula C24H25N5O3.
- Molecular weight 431.49 g/mol.
- Reported purity 99.6%.
- Available in small research pack sizes, including 25 mg.
Apexbio Technology LLC LDN 209929 dihydrochloride 50mg
LDN 209929 dihydrochloride is a small-molecule inhibitor targeting haspin kinase a serine/threonine kinase It is designed to inhibit haspin kinase activity thereby regulating chromosomal alignment and mitotic progression LDN 209929 dihydrochloride exerts its biological activity primarily through selective inhibition of haspin kinase It demonstrates an IC50 of approximately 55 nM and exhibits around 180-fold selectivity over DYRK2 kinase Based on these pharmacological properties LDN 209929 dihydrochloride holds research potential in oncology studies related to aberrant mitotic control and tumor cell proliferation