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122672-46-2

122672-46-2 | Cyclopentanecarboxylic acid, 2-amino-, (1R,2S)-

CAS No: 122672-46-2 Catalog No: AG0017LW MDL No:MFCD00882461

Product Description

Catalog Number:
AG0017LW
Chemical Name:
Cyclopentanecarboxylic acid, 2-amino-, (1R,2S)-
CAS Number:
122672-46-2
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
MDL Number:
MFCD00882461
IUPAC Name:
(1R,2S)-2-aminocyclopentane-1-carboxylic acid
InChI:
InChI=1S/C6H11NO2/c7-5-3-1-2-4(5)6(8)9/h4-5H,1-3,7H2,(H,8,9)/t4-,5+/m1/s1
InChI Key:
JWYOAMOZLZXDER-UHNVWZDZSA-N
SMILES:
N[C@H]1CCC[C@H]1C(=O)O
UNII:
Y1E02L9HC2

Properties

Complexity:
124  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
129.079g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
129.159g/mol
Monoisotopic Mass:
129.079g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
63.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-2  

Literature

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Adjuvant intra-arterial chemotherapy and radiotherapy versus surgery alone in resectable pancreatic and periampullary cancer: a prospective randomized controlled trial. Annals of surgery 20081201
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Establishing effective simulation protocols for beta- and alpha/beta-peptides. II. Molecular mechanical (MM) model for a cyclic beta-residue. The journal of physical chemistry. B 20080501
[Recent advances in the study of antifungal lead compounds with new chemical scaffolds]. Yao xue xue bao = Acta pharmaceutica Sinica 20071101
Effects of the alternating backbone configuration on the secondary structure and self-assembly of beta-peptides. Journal of the American Chemical Society 20061018
Beta-azidocyclopropanediesters: useful building blocks with potential application in agricultural and pharmaceutical chemistry. Communications in agricultural and applied biological sciences 20060101
Alicyclic beta-amino acids in Medicinal Chemistry. Amino acids 20050801
Kinetic resolution of tert-butyl (RS)-3-alkylcyclopentene-1-carboxylates for the synthesis of homochiral 3-alkyl-cispentacin and 3-alkyl-transpentacin derivatives. Organic & biomolecular chemistry 20041121
Parallel kinetic resolution of tert-butyl (RS)-3-alkyl-cyclopentene-1-carboxylates for the asymmetric synthesis of 3-alkyl-cispentacin derivatives. Organic & biomolecular chemistry 20041121
Accommodation of alpha-substituted residues in the beta-peptide 12-helix: expanding the range of substitution patterns available to a foldamer scaffold. Journal of the American Chemical Society 20030716
The use of enantiomerically pure ketene dithioacetal bis(sulfoxides) in highly diastereoselective intramolecular nitrone cycloadditions. Application in the total synthesis of the beta-amino acid (-)-cispentacin and the first asymmetric synthesis of cis-(3R,4R)-4-amino-pyrrolidine-3-carboxylic acid. Organic & biomolecular chemistry 20030221
Novel antifungal beta-amino acids: synthesis and activity against Candida albicans. Bioorganic & medicinal chemistry letters 20030210
Expression of angiogenic factors in hepatocellular carcinoma after transcatheter arterial chemoembolization. Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 20030101
A bicyclic cispentacin derivative as a novel reverse turn inducer in a GnRH mimetic. The Journal of organic chemistry 20021004
Mimicry of host-defense peptides by unnatural oligomers: antimicrobial beta-peptides. Journal of the American Chemical Society 20020626
Highly diastereoselective nitrone cycloaddition onto a chiral ketene equivalent: asymmetric synthesis of cispentacin. Organic letters 20020404
An efficient route to either enantiomer of trans-2-aminocyclopentanecarboxylic acid. The Journal of organic chemistry 20010810
Emerging novel antifungal agents. Drug discovery today 20000101
Beta-cyanoglutamic acid, a new antifungal amino acid from a streptomycete. The Journal of antibiotics 19930401
Anti-Candida activity of cispentacin: the active transport by amino acid permeases and possible mechanisms of action. Biochemical and biophysical research communications 19930215

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