D2521
(+)-顺式-地尔硫卓 盐酸盐
≥99% (HPLC), L-type Ca2+ channel blocker, powder
别名:
(2S,3S)-(+)-顺式-3-乙酰氧基-5-(2-二甲基氨基乙基)-2,3-二氢-2-(4-甲氧基苯基)-1,5-苯并硫氮杂-4(5H)- 酮 盐酸盐, CRD-401
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关于此项目
经验公式（希尔记法）:
C22H26N2O4S · HCl
化学文摘社编号:
分子量:
450.98
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
251-443-3
MDL number:
Beilstein/REAXYS Number:
4228706
产品名称
(+)-顺式-地尔硫卓 盐酸盐, ≥99% (HPLC)
InChI key
HDRXZJPWHTXQRI-BHDTVMLSSA-N
InChI
1S/C22H26N2O4S.ClH/c1-15(25)28-20-21(16-9-11-17(27-4)12-10-16)29-19-8-6-5-7-18(19)24(22(20)26)14-13-23(2)3;/h5-12,20-21H,13-14H2,1-4H3;1H/t20-,21+;/m1./s1
SMILES string
Cl.COc1ccc(cc1)[C@@H]2Sc3ccccc3N(CCN(C)C)C(=O)[C@@H]2OC(C)=O
assay
≥99% (HPLC)
form
powder
originator
Valeant
storage temp.
2-8°C
Quality Level
Gene Information
human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779)
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Application
(+)-顺式-盐酸地尔硫卓已用于:
- 研究其对整体分散基质（monolithic dispersion matrix）中扩散和释放的影响（26）
- 研究其在视网膜色素变性（RP）模型中的神经保护作用（27）
- 作为Cav1.2 L型钙通道（LTCC）的拮抗剂（28）
Biochem/physiol Actions
封闭缓慢或L-型Ca2+通道；调节来自中性粒细胞内存储的Ca2+的释放；刺激1,4-二氢吡啶结合至Ca2+通道；冠状动脉舒张剂。
Features and Benefits
这种化合物是环核苷酸研究的特色产品。点击此处发现更多特色环核苷酸产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
General description
盐酸地尔硫卓可用于治疗心血管疾病，例如心绞痛和高血压。它可充当细胞色素P450 3A（CYP3A）的抑制剂。地尔硫卓可能与斑丘疹、荨麻疹和瘙痒有关。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Diltiazem induces severe photodistributed hyperpigmentation: case series, histoimmunopathology, management, and review of the literature
Saladi RN, et al.
Archives of Dermatology, 142(2), 206-210 (2006)
D Dobrev et al.
British journal of pharmacology, 127(2), 576-582 (1999-06-29)
1. The putative inhibitory effects of verapamil and diltiazem on neuronal non-L-type Ca2+ channels were studied by investigating their effects on either K+- or veratridine-evoked [3H]-dopamine ([3H]-DA) release in rat striatal slices. Involvement of N-, P- and Q-type channels was
Andrés Pizzorno et al.
Cell reports. Medicine, 1(4), 100059-100059 (2020-08-25)
In the current COVID-19 pandemic context, proposing and validating effective treatments represents a major challenge. However, the scarcity of biologically relevant pre-clinical models of SARS-CoV-2 infection imposes a significant barrier for scientific and medical progress, including the rapid transition of
M J Gunthorpe et al.
The Journal of physiology, 519 Pt 3, 713-722 (1999-08-24)
1. To extend our knowledge of the site and mechanism of action of L-type Ca2+ channel antagonists on 5-HT3 receptors, whole-cell voltage clamp electrophysiology was used to investigate the action of one of these compounds, diltiazem, on the recombinant receptor
Effect of diltiazem on midazolam and alfentanil disposition in patients undergoing coronary artery bypass grafting
Ahonen J, et al.
Anesthesiology, 85(6), 1246-1252 (1996)
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