Substance
ID:1820245
Names and Identifiers
IUPAC name
(2R,3r,4S)-pentane-1,2,3,4,5-pentol
Synonyms
xylitol(2R,3R,4S)-Pentane-1,2,3,4,5-pentaolD-XYLITOLL-xylitolXylitXylitolxylitexylitol
IUPAC Traditional name
D-xylitol
Registration numbers
Beilstein Number
CAS Number
PubChem CID
Wikipedia Title
KEGG ID
MetaCyc Database
PubMed Citation Links
Reaxys Registry
BRENDA Database
1.1.3.43.1.1.725.3.1.52.4.1.115.1.3.35.3.1.255.3.1.35.3.1.43.2.1.263.2.1.12.4.1.71.1.1.3071.1.1.91.1.1.101.1.1.141.1.1.121.1.1.2501.1.3.411.1.1.B191.1.5.21.1.1.561.1.1.B641.1.1.111.1.1.2872.7.1.171.1.1.213.1.3.581.1.1.162.7.1.1221.1.1.4063.2.1.1393.2.1.371.1.1.721.1.1.1381.1.99.281.1.1.191.1.1.672.4.1.1623.2.1.521.1.1.2893.1.1.171.1.5.5
CHEMBL
CompTox Database
MetaboLights Database
MTBLS4722MTBLS519MTBLS522MTBLS530MTBLS459MTBLS545MTBLS601MTBLS442MTBLS533MTBLS552MTBLS662MTBLS606MTBLS612MTBLS615MTBLS642MTBLS801MTBLS697MTBLS687MTBLS872MTBLS4012MTBLS804MTBLS926MTBLS742MTBLS23MTBLS2279MTBLS2394MTBLS2878MTBLS112MTBLS106MTBLS893MTBLS95MTBLS2559MTBLS2542MTBLS1196MTBLS136MTBLS1463MTBLS145MTBLS135MTBLS1541MTBLS1561MTBLS171MTBLS181MTBLS180MTBLS1980MTBLS2017MTBLS201MTBLS208MTBLS359MTBLS3595MTBLS298MTBLS355MTBLS306MTBLS301MTBLS309MTBLS3322MTBLS353MTBLS1866MTBLS3627MTBLS370MTBLS360MTBLS3786MTBLS407MTBLS413MTBLS1906MTBLS220MTBLS2205MTBLS191MTBLS215
Protein Data Bank
SureChEMBL Database
UniProt Database
Q91XV4Q91X52Q920P0Q1JP75Q21929Q920N9Q7Z4W1Q8NK50Q8JIS3A1DEK3C5FSW4A1CAU3B0Y4D5B8NTI4Q4WUV8A2QMS4Q8X167Q2U3V4Q0CIL2Q5ASE0Q9FJ95P38715G4MZI3B0XNR0Q6Y0Z3B8N195O74237Q9P8R5Q4WJT9O13283Q2UKD0Q5BGA7A2Q8B5Q0CUL0C5FFQ7Q876L8A1CRI1Q8X195Q5GN51Q86ZV0Q0CWQ2P49378A1D4E3P78736O94735P31867C5FTT1P87039Q5ARL6A1CFY8B0YC65A1D9C9Q92MT4P22144Q8U7Y1Q59545Q98D10Q4WAU7P83049Q07993A2QY54Q9KX73Q8VZ80Q763T4Q96V44Q7SI09C5J3R8A2QJX5O42804Q5AVS0G4N708Q9P430Q9ZBU1
HMDB Database
PDBeChem Database
VirtualMetabolicHuman Database
Patent number
US2005131007US2005143410US2005163855US2005171070US2005255161US2006014819US2006025584US2006062847US2007160708US2007178054US2007178055US2007178123US2007178150US2007178151US2007178156US2007178158US2007178165US2007178166US2007183983US2007183985US2007185234US2007190087US2007191314US2007196474US2007196475US2007196476US2007196477US2007202184US2007207094US2007207202US2007207206US2007207956US2007208067US2007208069US2007212417US2007218114US2007218129US2007218130US2007224268US2007225348US2007231367US2007237816US2007243185US2007249576US2007254028US2007259038US2007259334US2007259808US2007269510US2008242721WO2005023198WO2005078060WO2005087692WO2007085835EP1803444EP1803450EP1806125EP1806130EP1818064EP1820497EP1852108EP1852109EP1852122EP1859791EP1867363EP1870102EP1880710EP1889611EP1894577EP1905444EP1905453EP1913937EP1923051EP1938806EP1941862EP1941878EP1944017EP1944025EP1946776EP1950205EP1952801EP1961409EP1961413EP1964547EP1967181EP1970050EP1977734EP1980272EP1982705EP1987821US2002153317US2002160467US2003021759US2003026774US2003097029US2003125588US2003130545US2004063980US2004170658US2004176319US2004213881US2005084506US2005096341US2005101546EP0918057EP0962459EP1004304EP1219604EP1366760EP1374871EP1498114EP1504673EP1504761EP1523974EP1527782EP1541134EP1547579EP1554936EP1563820EP1568356EP1570842EP1579771EP1579852EP1580229EP1582205EP1582221EP1591121EP1595533EP1598080EP1600155EP1604647EP1607087EP1616840EP1621187EP1627573EP1627642EP1637597EP1642591EP1645287EP1647269EP1652524EP1666030EP1669090EP1674098EP1681065EP1683417EP1685875EP1688131EP1693086EP1704847EP1712541EP1721620EP1741439EP1743629EP1747781EP1759695EP0856515EP1762232EP1785141EP1787640EP1790334EP1792939WO2007086039WO2007086846WO2007091856WO2007096902WO2007096906WO2007103528WO2007104575WO2007105179WO2007112286WO2007112574WO2007113885WO2007114791WO2007119185WO2007121545WO2007122146WO2007125541WO2007128724WO2007128983WO2007130373WO2007133508WO2007133509WO2007134870WO2007136830WO2008124458WO2008124749WO2008154221
EnzymePortal Database
GeneOntology Database
DrugBank ID
Drug Central Database
KEGG DRUG Database
Reactom Database
IEDB Database
Gmelin ID
PubChem SID
Properties
No Data Available
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Molecule Details
A pentitol (five-carbon sugar alcohol) having meso-configuration, being derived from xylose by reduction of the carbonyl group.
Molecular Spectra
No Data Available
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References
No Data Available
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