C4080
环庚米特
别名:
10,11-二氢-5H-二苯并(a,d)环庚烯-5-羧酰胺
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关于此项目
经验公式（希尔记法）:
C16H15NO
化学文摘社编号:
分子量:
237.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-570-8
MDL number:
Form:
powder
InChI key
APBVLLORZMAWKI-UHFFFAOYSA-N
InChI
1S/C16H15NO/c17-16(18)15-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H2,17,18)
SMILES string
NC(=O)C1c2ccccc2CCc3ccccc13
form
powder
Quality Level
Application
Used to study pharmacological activity involved in identification of compounds with central nervous system activity
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
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
[Determination of plasma lidocaine by gas-liquid chromatography].
I Saavedra et al.
Revista medica de Chile, 115(7), 661-664 (1987-07-01)
P W Codding et al.
Journal of medicinal chemistry, 27(5), 649-654 (1984-05-01)
The molecular structures of cyheptamide and 3-hydroxy-3- phenacyloxindole were determined by X-ray diffraction methods. The amide group in both compounds exhibits delocalization of the pi-electrons over the three atoms (N, C, and O), while the bond linking the amide to
G L Jones et al.
Journal of pharmaceutical sciences, 70(6), 618-620 (1981-06-01)
Carbamazepine and cyheptamide have certain stereochemical features in common with phenytoin; when superimposed, two bulky hydrophobic groups in each permit the approximate apposition of two electron donor atoms. The anticonvulsant activity of each compound was determined in mice using a
Josefin Koehn et al.
Antimicrobial agents and chemotherapy, 59(11), 6682-6688 (2015-08-08)
In the treatment of HIV infection, a combination of anti-HIV drugs is commonly used in highly active antiretroviral therapy (HAART). One such combination recommended for clinical therapy consists of the two HIV protease inhibitors atazanavir and ritonavir and the HIV
Anticonvulsant activities and brain concentrations of cyheptamide and carbamazepine.
G H Wimbish et al.
Proceedings of the Western Pharmacology Society, 23, 75-79 (1980-01-01)
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