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C4080

Sigma-Aldrich

Cyheptamide

Synonym(s):

10,11-Dihydro-5H-dibenzo(a,d)cycloheptene-5-carboxamide

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About This Item

Empirical Formula (Hill Notation):
C16H15NO
CAS Number:
7199-29-3
Molecular Weight:
237.30
EC Number:
230-570-8
MDL number:
MFCD00467136
UNSPSC Code:
12352100
PubChem Substance ID:
57654004
NACRES:
NA.22

form

powder

SMILES string

NC(=O)C1c2ccccc2CCc3ccccc13

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)

InChI key

APBVLLORZMAWKI-UHFFFAOYSA-N

Application

Used to study pharmacological activity involved in identification of compounds with central nervous system activity

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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)
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
[Determination of plasma lidocaine by gas-liquid chromatography].
I Saavedra et al.
Revista medica de Chile, 115(7), 661-664 (1987-07-01)
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
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
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