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(Z)-N'-(2-HYDROXY-3-(PIPERIDIN-1-YL)PROPOXY)NICOTINIMIDAMIDE DIHYDROCHLORIDE structure, CAS 66611-37-8

(Z)-N'-(2-HYDROXY-3-(PIPERIDIN-1-YL)PROPOXY)NICOTINIMIDAMIDE DIHYDROCHLORIDE

CAS Number66611-37-8

SynonymsBGP-15; (Z)-N'-(2-hydroxy-3-(piperidin-1-yl)propoxy)nicotiniMidaMide

Molecular FormulaC14H24Cl2N4O2

Molecular Weight351.27

Purity≥98 (HPLC)%

Density

Boiling Point

Melting Point

Flash Point

Appearancesolid

EINECS0

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-0102495 Purity: ≥98 (HPLC)%
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Quality Control of [ 66611-37-8 ] Purity: ≥98 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number66611-37-8
Catalog No.2A-0102495
Chinese Name(Z)-N-(2-羟基-3-(哌啶-1-基)丙氧基)烟酰胺双盐酸盐
SynonymsBGP-15; (Z)-N'-(2-hydroxy-3-(piperidin-1-yl)propoxy)nicotiniMidaMide
Molecular FormulaC14H24Cl2N4O2
Molecular Weight351.27
Purity≥98 (HPLC)
Appearancesolid
Storage Condition2-8°C
ApplicationBGP-15 is a PARP inhibitor with IC50 and Ki values ​​of 120 and 57 μM, respectively.
EINECS0
HTC2933399090
UN(IATA)0
PubChem ID329773244
MDL NumberMFCD21603901
SMILESCl.Cl.N\C(=N/OCC(O)CN1CCCCC1)c2cccnc2
InChI1S/C14H22N4O2.2ClH/c15-14(12-5-4-6-16-9-12)17-20-11-13(19)10-18-7-2-1-3-8-18;;/h4-6,9,13,19H,1-3,7-8,10-11H2,(H2,15,17);2*1H
InChI KeyISGGVCWFTPTHIX-UHFFFAOYSA-N
NACRES CodeNA.77
UNSPSC12352200
MSDSmsds/102495_1_66611_37_8.pdf
Use ofBGP-15 is a PARP inhibitor, with an IC50 and a Ki of 120 and 57 μM, respectively. Properties Name N-(2-Hydroxy-3-(piperidin-1-yl)propoxy)-nicotinimidamide dihydrochloride Synonym More Synonyms BGP-15 Biological Activity Description BGP-15 is a PARP inhibitor, with an IC50 and a Ki of 120 and 57 μM, respectively. Related Catalog Research Areas >> Cardiovascular Disease PARP:120 μM (IC50) In Vitro BGP-15 (200 μM) prevents the imatinib mesylate-induced oxidative damages, attenuates the depletion of high-energy phosphates, alters the signaling effect of imatinib mesylate by preventing p38 MAP kinase and JNK activation, and induced the phosphorylation of Akt and GSK-3beta[5]. References [1]. Kennedy TL, et al. BGP-15 Improves Aspects of the Dystrophic Pathology in mdx and dko Mice with Differing Efficacies in Heart and Skeletal Muscle. Am J Pathol. 2016 Dec;186(12):3246-3260. [2]. Salah H, et al. The chaperone co-inducer BGP-15 alleviates ventilation-induced diaphragm dysfunction. Sci Transl Med. 2016 Aug 3;8(350):350ra103 [3]. Sapra G, et al. The small-molecule BGP-15 protects against heart failure and atrial fibrillation in mice. Nat Commun. 2014 Dec 9;5:5705. [4]. Literati-Nagy B, et al. Improvement of insulin sensitivity by a novel drug candidate, BGP-15, in different animal studies. Metab Syndr Relat Disord. 2014 Mar;12(2):125-31. [5]. Sarszegi Z, et al. BGP-15, a PARP-inhibitor, prevents imatinib-induced cardiotoxicity by activating Akt and suppressing JNK and p38 MAP kinases. Mol Cell Biochem. 2012 Jun;365(1-2):129-37. [6]. Szabados E, et al. BGP-15, a nicotinic amidoxime derivate protecting heart from ischemia reperfusion injury through modulation of poly(ADP-ribose) polymerase. Biochem Pharmacol. 2000 Apr 15;59(8):937-45. Chemical & Physical Properties Exact Mass 350.12800 PSA 81.47000 LogP 2.80750 InChIKey ISGGVCWFTPTHIX-UHFFFAOYSA-N Safety Information HS Code 2933399090
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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