분석
≥99% (HPLC)
색상
yellow, powder
solubility
DMSO: 50 mg/mL, clear, yellow
SMILES string
O=C1CCC(=NN1)c2ccc(cc2)-n3ccnc3
InChI
1S/C13H12N4O/c18-13-6-5-12(15-16-13)10-1-3-11(4-2-10)17-8-7-14-9-17/h1-4,7-9H,5-6H2,(H,16,18)
InChI key
VXMYWVMXSWJFCV-UHFFFAOYSA-N
유전자 정보
human ... PDE3A(5139)
rat ... Pde3a(50678)
생화학적/생리학적 작용
Selective phoshodiesterase III (PDE3) inhibitor.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Journal of cyclic nucleotide and protein phosphorylation research, 11(7), 513-527 (1986-01-01)
Two approaches were taken to examine the role which the different forms of phosphodiesterase present in cardiac muscle play in regulating contractility. In an initial study, the effect of selective inhibitors of i) the calmodulin-stimulated phosphodiesterase (M & B 22
Journal of cardiovascular pharmacology, 16(1), 59-67 (1990-07-01)
Although recent studies indicate that MCI-154 exerts novel positive inotropic actions in heart muscle, the chronotropic properties of this new drug remain undefined. The present study compared the inotropic/chronotropic profile of MCI-154 with those of a nonselective beta 1/beta 2-agonist
Journal of cardiovascular pharmacology, 8(3), 520-526 (1986-05-01)
The purpose of this study was to evaluate the effect of the new cardiotonic, imazodan (CI-914), on myocardial hemodynamics and oxygen consumption, and peripheral blood flow distribution. Organ blood flow was measured by the radiolabeled-microsphere-reference-withdrawal technique and myocardial oxygen consumption
High-performance liquid chromatographic assay of imazodan, methylparaben and propylparaben in imazodan injection.
Journal of chromatography, 450(3), 407-413 (1988-10-26)
Molecular endocrinology (Baltimore, Md.), 5(12), 1947-1954 (1991-12-01)
Insulin-like growth factor-I (IGF-I) stimulated Xenopus laevis oocyte ribosomal S6 kinase activity 5- to 10-fold, with an apparent EC50 of 0.8 +/- 0.1 nM after 90 min of hormone treatment. IGF-I-stimulated enzyme activity was inhibited by treatment of oocytes with
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