Piperidines

Ambeed AMBEED

5000883015 1-BOC-4-METHYLPIPERIDINE 10G

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Ambeed AMBEED

5000882158 S-3-METHYLPIPERIDINE HYD 5G

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eMolecules​ 184637-48-7 | 1-Boc-3-aminopiperidine | Accela ChemBio (ASD) | MFCD01861219 | 200.282 | C10H20N2O2 | 97.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 5g | 510407191

1-Boc-3-aminopiperidine | Accela ChemBio (ASD) | 184637-48-7 | MFCD01861219 | 200.282 | C10H20N2O2 | 97.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 5g | 510407191

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eMolecules​ 184637-48-7 | 1-Boc-3-aminopiperidine | Accela ChemBio (ASD) | MFCD01861219 | 200.282 | C10H20N2O2 | 97.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 100g | 533771330

1-Boc-3-aminopiperidine | Accela ChemBio (ASD) | 184637-48-7 | MFCD01861219 | 200.282 | C10H20N2O2 | 97.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 100g | 533771330

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Medchemexpress LLC HY-111151 5mg Medchemexpress, AR-9281 CAS:913548-29-5 Purity:>98%

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Medchemexpress, HY-111151 5mg AR-9281 CAS:913548-29-5 AR9281 is a potent and selective inhibitor of soluble epoxide hydrolase (s-EH) , with potential for the treatment of hypertension and type 2 diabetes [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.

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eMolecules​ 184637-48-7 | 1-Boc-3-aminopiperidine | ChemScene | MFCD01861219 | 200.282 | C10H20N2O2 | 98.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 25g | 572221649

1-Boc-3-aminopiperidine | ChemScene | 184637-48-7 | MFCD01861219 | 200.282 | C10H20N2O2 | 98.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 25g | 572221649

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eMolecules​ 625471-18-3 | (S)-1-Boc-3-aminopiperidine | AA Blocks LLC | MFCD01861219 | 200.282 | C10H20N2O2 | 0.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 1g | 410163245

(S)-1-Boc-3-aminopiperidine | AA Blocks LLC | 625471-18-3 | MFCD01861219 | 200.282 | C10H20N2O2 | 0.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 1g | 410163245

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Medchemexpress LLC HY-112167A 5mg Medchemexpress, GDC-0575 dihydrochloride CAS:1657014-42-0 Purity:>98%

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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.

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Selleck Chemical LLC Encenicline (EVP-6124) hydrochloride S2957-5mg

Encenicline (EVP-6124) hydrochloride is a selective 7 nicotinic acetylcholine receptor partial agonist improves memory performance by potentiating the acetylcholine response of 7 nicotinic acetylcholine receptors

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Medchemexpress LLC HY-117291A 10mg Medchemexpress, XMD-17-51 Trifluoroacetate CAS: Purity:>98%

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Medchemexpress, HY-N0171A 25mg Beta-Sitosterol (purity>98%) CAS:83-46-5 Beta-Sitosterol (purity>98%) is a plant sterol. Beta-Sitosterol (purity>98%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation. 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.

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eMolecules​ 120278-07-1 | 1-N-Cbz-4-Aminopiperidine | ChemScene | MFCD05863884 | 234.299 | C13H18N2O2 | 97.000 | NC1CCN(CC1)C(=O)OCc1ccccc1 | 10g | 536844644

1-N-Cbz-4-Aminopiperidine | ChemScene | 120278-07-1 | MFCD05863884 | 234.299 | C13H18N2O2 | 97.000 | NC1CCN(CC1)C(=O)OCc1ccccc1 | 10g | 536844644

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Medchemexpress LLC K-Ras-PDE -IN-1 | 10MG

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K-Ras-PDE -IN-1 is a novel and potent competitive K-Ras-PDE inhibitor K-Ras-PDE -IN-1 binds to the farnesyl binding pocket of PDE with a low nanomolar Kd of 8 nM[1]

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Medchemexpress LLC Btk inhibitor 2 (BGB-3111 analog) | 1558036-85-3 | MFCD31382019 | 99.6% | 431.49 g/mol | C24H25N5O3 | 25 MG

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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.

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eMolecules​ 184637-48-7 | 1-Boc-3-aminopiperidine | Combi-Blocks | MFCD01861219 | 200.282 | C10H20N2O2 | 97.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 25g | 117518457

1-Boc-3-aminopiperidine | Combi-Blocks | 184637-48-7 | MFCD01861219 | 200.282 | C10H20N2O2 | 97.000 | CC(C)(C)OC(=O)N1CCCC(N)C1 | 25g | 117518457

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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

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