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关于此项目
经验公式(希尔记法):
C9H10N4O4
化学文摘社编号:
分子量:
238.20
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-490-2
Beilstein/REAXYS Number:
279221
MDL number:
Assay:
≥99.0% (T)
Form:
powder
InChI key
HCYFGRCYSCXKNQ-UHFFFAOYSA-N
InChI
1S/C9H10N4O4/c1-11-7-6(8(16)12(2)9(11)17)13(4-10-7)3-5(14)15/h4H,3H2,1-2H3,(H,14,15)
SMILES string
CN1C(=O)N(C)c2ncn(CC(O)=O)c2C1=O
assay
≥99.0% (T)
form
powder
Gene Information
human ... ADORA2B(136)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Gas-liquid chromatographic determination of acephylline in urine.
J Zuidema et al.
Journal of chromatography, 182(3-4), 445-447 (1980-06-13)
Alaa El-Gindy et al.
Journal of pharmaceutical and biomedical analysis, 43(3), 973-982 (2006-10-19)
Three methods are developed for the determination of two multicomponent mixtures containing guaiphenesine (GU) with salbutamol sulfate (SL), methylparaben (MP) and propylparaben (PP) [mixture 1]; and acephylline piperazine (AC) with bromhexine hydrochloride (BX), methylparaben (MP) and propylparaben (PP) [mixture 2].
K Primbs
Clinical therapeutics, 7(6), 733-736 (1985-01-01)
In an open study, 50 patients suffering from chronic obstructive pulmonary disease in an acute infectious phase were treated with ambroxol theophyllinacetate. The drug was given orally in a dosage of 100 mg BID for ten days. Viscosimetric data showed
[Amides of 7-theophyllineacetic acid with antiarrhythmic action].
M Eckstein et al.
Acta poloniae pharmaceutica, 44(1), 12-15 (1987-01-01)
G Dănilă et al.
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 94(3-4), 581-586 (1990-10-01)
Some esters of 7-theophyllinylacetic acid were synthetized, characterized physicochemically and tested for their anti-inflammatory properties. As compared to indomethacin, reference anti-inflammatory drug, all synthetized compounds were less toxic. The anti-inflammatory properties are influenced by the nature of the ester group
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