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Merck
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重要文件

S9384

Supelco

舒洛地尔

analytical standard, for drug analysis

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About This Item

經驗公式(希爾表示法):
C20H35NOS
CAS號碼:
分子量::
337.56
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

forensics and toxicology
pharmaceutical (small molecule)
veterinary

形式

neat

儲存溫度

2-8°C

SMILES 字串

CCCCCCCCN[C@H](C)[C@@H](O)c1ccc(SC(C)C)cc1

InChI

1S/C20H35NOS/c1-5-6-7-8-9-10-15-21-17(4)20(22)18-11-13-19(14-12-18)23-16(2)3/h11-14,16-17,20-22H,5-10,15H2,1-4H3/t17-,20-/m1/s1

InChI 密鑰

BFCDFTHTSVTWOG-YLJYHZDGSA-N

應用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

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Combination of suloctidil and anticoagulation in the prevention of reocclusion after femoro-popliteal PTA.
F Mahler et al.
VASA. Zeitschrift fur Gefasskrankheiten, 16(4), 381-385 (1987-01-01)
P Kontro et al.
Neuroscience, 19(3), 1007-1010 (1986-11-01)
The effects of taurine and its structural analogues and two new anticonvulsant derivatives, taltrimide and MY-103, on the function of brain dopaminergic systems were studied by assessing their interference with the binding of [3H]spiperone to synaptic membranes isolated from rat
J M Boeynaems et al.
Biochemical pharmacology, 36(10), 1629-1635 (1987-05-15)
Suloctidil is a calcium antagonist with vascular relaxing activity and an antithrombotic agent: its antiplatelet action has been demonstrated in vivo, but is difficult to reproduce in vitro and the mechanism of this effect remains unknown. We have observed that
C Mazière et al.
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 26(1), 3-6 (1988-01-01)
Human foetal lung fibroblasts were pretreated for 24 h with the antithrombotic drug, suloctidil (1 to 10 mumol/l), which induced a dose-dependent increase in LDL binding, uptake and degradation. At 10 mumol/l suloctidil, the respective increases in these parameters were
Beini Zeng et al.
Oncotarget, 8(41), 69972-69982 (2017-10-21)
As the most frequent fungal pathogen in humans

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