440841
(1R,2S)-(+)-顺式-1-氨基-2-茚醇
99%
别名:
(1R,2S)-(+)-顺式-1-氨基-2-茚满醇
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关于此项目
经验公式（希尔记法）:
C9H11NO
化学文摘社编号:
分子量:
149.19
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2803743
产品名称
(1R,2S)-(+)-顺式-1-氨基-2-茚醇, 99%
InChI
1S/C9H11NO/c10-9-7-4-2-1-3-6(7)5-8(9)11/h1-4,8-9,11H,5,10H2/t8-,9+/m0/s1
SMILES string
N[C@H]1[C@@H](O)Cc2ccccc12
InChI key
LOPKSXMQWBYUOI-DTWKUNHWSA-N
assay
99%
form
solid
optical activity
[α]22/D +63°, c = 0.2 in chloroform
optical purity
ee: 99% (GLC)
mp
118-121 °C (lit.)
functional group
hydroxyl
Quality Level
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Application
该 顺式 -氨基茚满醇及其对映异构体已用于制备一系列有效的 HIV-1 蛋白酶抑制肽。 此外，它们被用作手性配体用于硼烷催化的前手性酮的不对称还原。
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 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Askin, D. et al.
The Journal of Organic Chemistry, 57, 2771-2771 (1992)
D'Aniello, F. et al.
The Journal of Organic Chemistry, 59, 3762-3762 (1994)
Dorsey, B.D. et al.
Tetrahedron Letters, 34, 1851-1851 (1993)
S D Young et al.
Journal of medicinal chemistry, 35(10), 1702-1709 (1992-05-15)
A systematic investigation was undertaken to determine the role of the P1' sidechain in a series of hydroxyethylene isostere based inhibitors of HIV-1 protease. Substitution and homologation of the benzyl P1' side chain of the Phe-Phe isostere based pseudo peptides
S Thaisrivongs et al.
Journal of medicinal chemistry, 36(8), 941-952 (1993-04-16)
A number of potential HIV protease inhibitory peptides that contain the dihydroxyethylene isostere were prepared and evaluated for their enzyme binding affinity and antiviral activity in cell cultures. From the template of a previously reported active peptide A, modifications at
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