NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(2R,3S,5R)-2,5-bis(hydroxymethyl)pyrrolidine-3,4-diol
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IUPAC Traditional name
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(2R,3S,5R)-2,5-bis(hydroxymethyl)pyrrolidine-3,4-diol
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Synonyms
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2R,5R-Bis(hydroxymethyl)-3R,4R-dihydroxypyrrolidine
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(2R,3R,4R,5R)-3,4-Dihydroxy-2,5-pyrrolidinedimethanol
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2,5-Anhydro-2,5-imino-D-mannitol
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2,5-Dideoxy-2,5-imino-D-mannitol
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CAS Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
Data Source
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Data ID
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Price
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TRC
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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13.180374
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H Acceptors
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5
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H Donor
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5
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LogD (pH = 5.5)
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-5.8919373
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LogD (pH = 7.4)
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-4.375834
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Log P
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-2.8857431
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Molar Refractivity
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36.5744 cm3
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Polarizability
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15.1906805 Å3
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Polar Surface Area
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92.95 Å2
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Rotatable Bonds
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2
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
TRC
Toronto Research Chemicals -
D440000
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A glucosidase inhibitor. |
Toronto Research Chemicals -
A648350
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Many pyrrolidines are powerful inhibitors of glycohydrolases, enzymes responsible for cleavage of glycosidic bonds, glycoprotein processing and the gastrointestinal breakdown of dietary carbohydrates. These compounds are charged at physiological pH and |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Fellows, L.E.: Pestic. Sci., 17, 602 (1986)
- • Fellows, L.E., et al.: J. Chem. Brit., 287, (1987)
- • Elbein, A.D.: Annu. Rev. Biochem., 56, 497 (1987)
- • Fleet, G.W., et al.: J. Chem. Brit., 287, (1989) Baxter, E.W., et al.: J. Org. Chem., 59, 3175 (1987)
- • Tyms, A.S. et al. Lancet 1025, (1987)
- • Spearman,
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PATENTS
PATENTS
PubChem Patent
Google Patent