A6883
Atropine methyl bromide
≥99% (TLC), powder
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C18H26NO3 · Br
Numer CAS:
Masa cząsteczkowa:
384.31
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
220-700-1
MDL number:
Pomoc techniczna
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Pozwól nam pomócassay
≥99% (TLC)
form
powder
color
white to off-white
solubility
H2O: 50 mg/mL
SMILES string
Br.C[N]1(C)[C@@H]2CC[C@H]1C[C@@H](C2)OC(=O)C(CO)c3ccccc3
InChI
1S/C18H26NO3.BrH/c1-19(2)14-8-9-15(19)11-16(10-14)22-18(21)17(12-20)13-6-4-3-5-7-13;/h3-7,14-17,20H,8-12H2,1-2H3;1H/t14-,15+,16?,17?;
InChI key
YBFLMRSYEWDJEJ-ZNHDNBJUSA-N
Gene Information
human ... CHRM1(1128), CHRM2(1129), CHRM3(1131), CHRM4(1132), CHRM5(1133)
Biochem/physiol Actions
Competitive muscarinic acetylcholine receptor antagonist that does not cross the blood-brain barrier.
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Timothy A Yap et al.
Molecular cancer therapeutics, 10(2), 360-371 (2010-12-31)
AKT is frequently deregulated in cancer, making it an attractive anticancer drug target. CCT128930 is a novel ATP-competitive AKT inhibitor discovered using fragment- and structure-based approaches. It is a potent, advanced lead pyrrolopyrimidine compound exhibiting selectivity for AKT over PKA
M M Knuepfer et al.
The American journal of physiology, 276(1 Pt 2), R103-R112 (1999-01-14)
It has been suggested that toxicity to cocaine is related to the relative rate of cocaine metabolism by cholinesterases and to activation of cholinergic receptors either directly or by reflex mechanisms. We examined these possibilities by altering cholinesterase activity and
H Ohnuma et al.
Journal of the autonomic nervous system, 57(1-2), 43-48 (1996-02-05)
Hepatic glucoreceptor-vagal afferent inputs to the central nervous system and pancreatic vagal efferent stimuli are important for insulin secretion. In the present study, we examined the effect of intracerebroventricular (i.c.v.) injection of atropine methyl bromide (methylatropine) on the insulin response