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(S)-(−)-Aminoglutethimide - 97%, high purity , CAS No.57288-03-6
Basic Description
Synonyms
(-)-(S)-Aminoglutethimide | NCGC00016379-01 | PS-18882 | CAS-125-84-8 | SCHEMBL116988 | D-Aminoglutethimide | UNII-5S1T2OED7F | (S)-(-)-Aminoglutethimide, 97% | F89425 | NCGC00015110-01 | Q27124214 | (S)-(-)-Aminoglutethimide | (S)-()-Aminoglutethimide |
Specifications & Purity
≥97%
Product Description
Description
(S)-(−)-Aminoglutethimide can be used:As an internal standard in the separation of the pyridoglutethimide enantiomers using the HPLC technique.In the study of steroid hormones role on human cytomegalovirus replication in adrenocortical cells.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Piperidines
Subclass
Phenylpiperidines
Intermediate Tree Nodes
Not available
Direct Parent
Phenylpiperidines
Alternative Parents
Piperidinediones Aniline and substituted anilines Delta lactams N-unsubstituted carboxylic acid imides Dicarboximides Amino acids and derivatives Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenylpiperidine - Piperidinedione - Aniline or substituted anilines - Delta-lactam - Piperidinone - Monocyclic benzene moiety - Benzenoid - Carboxylic acid imide - Dicarboximide - Carboxylic acid imide, n-unsubstituted - Lactam - Amino acid or derivatives - Carboxylic acid derivative - Azacycle - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Amine - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as phenylpiperidines. These are compounds containing a phenylpiperidine skeleton, which consists of a piperidine bound to a phenyl group.
External Descriptors
aminoglutethimide
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
(3S)-3-(4-aminophenyl)-3-ethylpiperidine-2,6-dione
INCHI
InChI=1S/C13H16N2O2/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9/h3-6H,2,7-8,14H2,1H3,(H,15,16,17)/t13-/m0/s1
InChIKey
ROBVIMPUHSLWNV-ZDUSSCGKSA-N
Smiles
CCC1(CCC(=O)NC1=O)C2=CC=C(C=C2)N
Isomeric SMILES
CC[C@]1(CCC(=O)NC1=O)C2=CC=C(C=C2)N
WGK Germany
3
Molecular Weight
232.28
Reaxy-Rn
210656
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=210656&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Molecular Weight
232.280 g/mol
XLogP3
1.200
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
232.121 Da
Monoisotopic Mass
232.121 Da
Topological Polar Surface Area
72.200 Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
321.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
1
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
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