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Merck
모든 사진(2)

주요 문서

D0676

Sigma-Aldrich

Dobutamine hydrochloride

≥98% (TLC), powder, α1, β1 and β2-adrenoceptor agonist

동의어(들):

(±)-3,4-Dihydroxy-N-[3-(4-hydroxyphenyl)-1-methylpropyl]-β-phenethylamine hydrochloride

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About This Item

실험식(Hill 표기법):
C18H23NO3 · HCl
CAS Number:
Molecular Weight:
337.84
EC Number:
MDL number:
UNSPSC 코드:
12352116
PubChem Substance ID:
NACRES:
NA.77

product name

Dobutamine hydrochloride, ≥98%

Quality Level

분석

≥98%

형태

powder

주관자

Eli Lilly

저장 온도

2-8°C

SMILES string

Cl[H].CC(CCc1ccc(O)cc1)NCCc2ccc(O)c(O)c2

InChI

1S/C18H23NO3.ClH/c1-13(2-3-14-4-7-16(20)8-5-14)19-11-10-15-6-9-17(21)18(22)12-15;/h4-9,12-13,19-22H,2-3,10-11H2,1H3;1H

InChI key

BQKADKWNRWCIJL-UHFFFAOYSA-N

유전자 정보

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Dobutamine hydrochloride has been used:
  • to treat mouse embryonic fibroblasts for cell death analysis
  • to inhibit TAZ (transcriptional coactivator with PDZ-binding motif)/YAP (Yes-associated protein) of Hippo pathway and study its effect on tumor cell proliferation
  • as β1-AR partial agonist to determine its effects on budding of endophilin-mRFP-positive structures by live-cell imaging

생화학적/생리학적 작용

Dobutamine is a synthetic catecholamine that stimulate the β1 -adrenoceptor receptor. It exhibits inotropic outcome on the myocardium. Dobutamine elevates contractility and is known to be useful in the condition of low blood pressure.

특징 및 장점

This compound was developed by Eli Lilly. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

픽토그램

Health hazardExclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

개인 보호 장비

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


시험 성적서(COA)

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Role of p53 in cAMP/PKA pathway mediated apoptosis
Rahimi A, et al.
Apoptosis, 18(12), 1492-1499 (2013)
Programming of Schwann cells by Lats1/2-TAZ/YAP signaling drives malignant peripheral nerve sheath tumorigenesis
Wu LMN, et al.
Cancer Cell, 33(2), 292-308 (2018)
Workbook in Practical Neonatology, 239-239 (2014)
Y Huang et al.
Clinical and experimental pharmacology & physiology, 25(6), 405-411 (1998-07-23)
1. In order to examine the possible involvement of the endothelium and K+ channel activation in the relaxation induced by dobutamine, a beta 1-adrenoceptor agonist, in rat isolated mesenteric arteries, the effects of inhibitors of nitric oxide (NO) activity, blockers
Dobutamine (2018)

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