- 関
- nicardipine
WordNet
- a complex consisting of an organic base in association with hydrogen chloride
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/10/20 16:53:07」(JST)
[Wiki en表示]
Nicardipine
|
Systematic (IUPAC) name |
2-[benzyl(methyl)amino]ethyl methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate |
Clinical data |
Trade names |
Cardene |
AHFS/Drugs.com |
monograph |
MedlinePlus |
a695032 |
Pregnancy cat. |
? |
Legal status |
℞ Prescription only |
Routes |
Oral, intravenous |
Pharmacokinetic data |
Protein binding |
>95% |
Half-life |
8.6 hours |
Identifiers |
CAS number |
55985-32-5 Y |
ATC code |
C08CA04 |
PubChem |
CID 4474 |
IUPHAR ligand |
2559 |
DrugBank |
DB00622 |
ChemSpider |
4319 Y |
UNII |
CZ5312222S Y |
KEGG |
D08270 Y |
ChEMBL |
CHEMBL1484 Y |
Chemical data |
Formula |
C26H29N3O6 |
Mol. mass |
479.525 g/mol |
SMILES
- O=C(OCCN(Cc1ccccc1)C)\C2=C(\N/C(=C(/C(=O)OC)C2c3cccc([N+]([O-])=O)c3)C)C
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InChI
-
InChI=1S/C26H29N3O6/c1-17-22(25(30)34-4)24(20-11-8-12-21(15-20)29(32)33)23(18(2)27-17)26(31)35-14-13-28(3)16-19-9-6-5-7-10-19/h5-12,15,24,27H,13-14,16H2,1-4H3 Y
Key:ZBBHBTPTTSWHBA-UHFFFAOYSA-N Y
|
Physical data |
Melt. point |
136-138 °C (-80 °F) |
Y (what is this?) (verify)
|
Nicardipine hydrochloride (Cardene) is a medication used to treat high blood pressure and angina. It belongs to the class of calcium channel blockers.
Nicardipine is a dihydropyridine calcium-channel blocking agent used for the treatment of vascular disorders such as chronic stable angina, hypertension, and Raynaud's phenomenon. It is available in oral and intravenous formulations. Its mechanism of action and clinical effects closely resemble those of nifedipine and the other dihydropyridines (amlodipine, felodipine), except that nicardipine is more selective for cerebral and coronary blood vessels. Furthermore, nicardipine does not intrinsically decrease myocardial contractility and may be useful in the management of congestive heart failure. Nicardipine also has a longer half-life than nifedipine. Nicardipine was approved by the FDA in December 1988. The patent for both Cardene and Cardene SR expired in October 1995.
It has been used in percutaneous coronary intervention.[1] Nicardipine is also an option for lowering of blood pressure in stroke patients who require blood pressure lowering prior to administration of Alteplase when blood pressure is >185/110. Also may be used during rtPA therapy when blood pressure is >230/120.
Nicardipine must be used with caution in patients with renal failure because of possible kidney shutdown.
Nicardipine inhibits the transmembrane influx of calcium ions into cardiac muscle and smooth muscle without changing serum calcium concentrations. The contractile processes of cardiac muscle and vascular smooth muscle are dependent upon the movement of extracellular calcium ions into these cells through specific ion channels. The effects of nicardipine are more selective to vascular smooth muscle than cardiac muscle. In animal models, nicardipine produced relaxation of coronary vascular smooth muscle at drug levels which cause little or no negative inotropic effect.
References[edit]
- ^ Huang RI, Patel P, Walinsky P, et al. (November 2006). "Efficacy of intracoronary nicardipine in the treatment of no-reflow during percutaneous coronary intervention". Catheter Cardiovasc Interv 68 (5): 671–6. doi:10.1002/ccd.20885. PMID 17034064.
Channel blockers
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Calcium (Ca2+) |
|
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Potassium (K+) |
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- Vernakalant
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|
Sodium (Na+) |
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- Sodium valproate
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- Toxins: Conotoxins
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Other |
- Uncategorized: Ethadione
- Paramethadione
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- Pheneturide
- Trimethadione
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UpToDate Contents
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English Journal
- Cholesterol reduces the sensitivity to platinum-based chemotherapy via upregulating ABCG2 in lung adenocarcinoma.
- Wu Y1, Si R2, Tang H1, He Z1, Zhu H1, Wang L1, Fan Y3, Xia S4, He Z5, Wang Q6.
- Biochemical and biophysical research communications.Biochem Biophys Res Commun.2015 Jan 17. pii: S0006-291X(15)00057-1. doi: 10.1016/j.bbrc.2015.01.035. [Epub ahead of print]
- Inoperable lung adenocarcinoma is currently treated with platinum-based chemotherapy. However, the effectiveness of these chemotherapeutic agents is not the same for all patients. Patients either show quick chemoresistance (QCR) or delayed chemoresistance (DCR), which are defined by 87 and 242 days
- PMID 25603057
- Intrathecal application of the nimodipine slow-release microparticle system eg-1962 for prevention of delayed cerebral ischemia and improvement of outcome after aneurysmal subarachnoid hemorrhage.
- Etminan N1, Macdonald RL, Davis C, Burton K, Steiger HJ, Hänggi D.
- Acta neurochirurgica. Supplement.Acta Neurochir Suppl.2015;120:281-6. doi: 10.1007/978-3-319-04981-6_47.
- The effective reduction of delayed cerebral ischemia (DCI), a main contributor for poor outcome following aneurysmal subarachnoid hemorrhage (SAH), remains challenging. Previous clinical trials on systemic pharmaceutical treatment of SAH mostly failed to improve outcome, probably because of insensit
- PMID 25366637
- Effects of diltiazem on sympathetic activity in patients with aneurysmal subarachnoid hemorrhage.
- Ogura T1, Takeda R, Ooigawa H, Nakajima H, Kurita H.
- Acta neurochirurgica. Supplement.Acta Neurochir Suppl.2015;120:47-50. doi: 10.1007/978-3-319-04981-6_8.
- This study evaluated the effect of diltiazem, a calcium antagonist, on sympathetic activity in patients with aneurysmal subarachnoid hemorrhage (SAH) during the hyperacute stage. Of patients with aneurysmal SAH who underwent aneurysm repair between August 2008 and June 2011, 119 consecutive patients
- PMID 25366598
Japanese Journal
- A Novel Rapid Quantitative Analysis of Drug Migration on Tablets Using Laser Induced Breakdown Spectroscopy
- Yokoyama Makoto,Tourigny Martine,Moroshima Kenji [他],Suzuki Junsuke,Sakai Miyako,Iwamoto Kiyoshi,Takeuchi Hirofumi
- Chemical and Pharmaceutical Bulletin 58(11), 1521-1524, 2010
- … To evaluate drug migration, model tablets containing nicardipine hydrochloride as active pharmaceutical ingredient (API) were prepared by a conventional wet granulation method. …
- NAID 130000405669
- 全身麻酔中に塩酸ニカルジピン投与が原因と思われる低酸素血症をきたした肥満患者の1例
- 佐藤 健一,久慈 昭慶,佐藤 裕,坂本 望,鍋島 謙一,西 健,鹿島 悠子,四戸 豊,佐藤 雅仁,城 茂治
- 日本歯科麻酔学会雑誌 = JOURNAL OF JAPANESE DENTAL SOCIETY OF ANESTHESIOLOGY 35(3), 396-397, 2007-07-15
- NAID 10019533019
- INDUCTION OF HEPATIC CYTOCHROME P450 ISOFORMS BY NICARDIPINE AT THERAPEUTIC DOSES IN SPONTANEOUSLY HYPERTENSIVE RATS
- Miyajima Shoji,Nemoto Kiyomitsu,Sekimoto Masashi [他],KINAE Yusuke,KASAHARA Toshihiko,SOUMA Shinji,DEGAWA Masakuni
- Journal of toxicological sciences 32(1), 79-90, 2007-02-16
- … Nicardipine hydrochloride (Nic), a calcium channel antagonist, is used for the treatment of hypertension. …
- NAID 110006204881
Related Links
- Nicardipine HCl is a calcium ion influx inhibitor (slow channel blocker or calcium channel blocker). Nicardipine HCl injection for intravenous administration contains 2.5 mg/mL of nicardipine hydrochloride. Nicardipine hydrochloride is a ...
- DESCRIPTION Cardene ® (nicardipine HCI) is a calcium ion influx inhibitor (slow channel blocker or calcium channel blocker). Cardene ® I.V. for intravenous administration contains 2.5 mg/mL of nicardipine hydrochloride. Nicardipine ...
- Hypotension or Tachycardia : If there is concern of impending hypotension or tachycardia, the infusion should be discontinued. When blood pressure has stabilized, infusion of nicardipine hydrochloride injection may be restarted at low ...
★リンクテーブル★
[★]
- 英
- nicardipine
- 化
- ニカルジピン塩酸塩 塩酸ニカルジピン nicardipine hydrochloride
- 商
- アポジピン、イセジピール、コポネント、サリペックス、ツルセピン、ニカジルスL、ニカルジレート、ニカルピン、ニコデール、ニスタジール、ペルジピン、ラジストミン
- 関
- カルシウム拮抗薬
- 血圧降下剤
分類
[★]
塩酸塩、ハイドロクロライド