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Anisodamine

Supplier:
Catalogue number:
a5334-5 g
Size:
5 g
Product is available in:
  • UK
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£336.00 Estimated delivery Tue 28 Sep
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Tropane alkaloid found in Solanaceae plants; α1-adrenergic and mAChR antagonist.

Product Type:

Proteins and peptides

CAS Number:

55869-99-3

Alternative Names:

6-Hydroxy hyoscyamine, race-Anidosamine, Raceanisodamine

Storage Temp:

Ambient

Compound Purity:

≥97%

Molecular Weight:

305.37

Reference:

Wang W, Chen QF, Li QB, et al. Efficiency of anisodamine for organophosphorus-poisoned patients when atropinization cannot be achieved with high doses of atropine. Environ Toxicol Pharmacol. 2014 Mar;37(2):477-81. PMID: 24561530. Guoshou Z, Chengye Z, Zhihui L, et al. Effects of high dose of anisodamine on the respiratory function of patients with traumatic acute lung injury. Cell Biochem Biophys. 2013 Jun;66(2):365-9. PMID: 23504631. Geng W, Fu XH, Gu XS, et al. Preventive effects of anisodamine against contrast-induced nephropathy in type 2 diabetics with renal insufficiency undergoing coronary angiography or angioplasty. Chin Med J (Engl). 2012 Oct;125(19):3368-72. PMID: 23044290. Zhang ZX, Wang P, Zhang QS, et al. Effects of anisodamine on the expressions of vascular endothelial growth factor and intercellular adhesion molecule 1 in experimental infusion phlebitis. Chin Med J (Engl). 2012 Jan;125(2):300-5. PMID: 22340563. Zhang WW, Song MK, Cui YY, et al. Differential neuropsychopharmacological influences of naturally occurring tropane alkaloids anisodamine versus scopolamine. Neurosci Lett. 2008 Oct 10;443(3):241-5. PMID: 18672024. Varma DR, Yue TL. Adrenoceptor blocking properties of atropine-like agents anisodamine and anisodine on brain and cardiovascular tissues of rats. Br J Pharmacol. 1986 Mar;87(3):587-94. PMID: 2879586.

Structure:

C17H23NO4

Formula:

C17H23NO4

UNSPSC Code:

12352202

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