Lactulose (CED0002549)

Record Information
Version1.0
Creation Date2016-05-22 05:21:47 UTC
Update Date2026-05-14 16:42:59 UTC
Accession NumberCHEM018585
Identification
Common NameLactulose
ClassSmall Molecule
Description
Lactulose is an organic compound with the formula C12H22O11 and an average molecular weight of 342.30 g/mol. Lactulose belongs to the carbohydrates and carbohydrate conjugates, a subclass of organooxygen compounds within the organic compounds. In industrial applications, this compound serves as a humectant, softener, and conditioner. It is found in healthcare, pharmaceuticals, and veterinary products as a drug for constipation, and it is also used in building and construction for ceilings. Recorded exposure routes for lactulose include oral and rectal administration. Regarding its biological activity, the compound has one recorded protein target, which is the other of Evolved beta-galactosidase subunit alpha (ebgA).
Contaminant TypeNot Available
Chemical Structure
Synonyms
ValueSource
4-O-beta-D-Galactopyranosyl-D-fructofuranoseChEBI
4-O-beta-D-Galactopyranosyl-D-fructoseChEBI
D-LactuloseChEBI
LactulosaChEBI
LactulosumChEBI
CephulacKegg
ChronulacKegg
4-O-b-D-Galactopyranosyl-D-fructofuranoseGenerator
4-O-Β-D-galactopyranosyl-D-fructofuranoseGenerator
4-O-b-D-Galactopyranosyl-D-fructoseGenerator
4-O-Β-D-galactopyranosyl-D-fructoseGenerator
(2S,3R,4S,5R,6R)-2-[(2R,3S,4S,5R)-4,5-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triolHMDB
4-O-beta-delta-Galactopyranosyl-delta-fructofuranoseHMDB
4-O-beta-delta-Galactopyranosyl-delta-fructoseHMDB
BifiteralHMDB
delta-LactuloseHMDB
NormaseHMDB
AmivalexHMDB
DuphalacHMDB
Chemical FormulaC12H22O11
Average Molecular Mass342.297 g/mol
Monoisotopic Mass342.116 g/mol
CAS Registry Number4618-18-2
IUPAC Name(2S,3R,4S,5R,6R)-2-{[(2R,3S,4S,5R)-4,5-dihydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
Traditional Namelactulose
SMILESOC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
InChI IdentifierInChI=1S/C12H22O11/c13-1-4-6(16)7(17)8(18)11(21-4)22-9-5(2-14)23-12(20,3-15)10(9)19/h4-11,13-20H,1-3H2/t4-,5-,6+,7+,8-,9-,10+,11+,12-/m1/s1
InChI KeyJCQLYHFGKNRPGE-FCVZTGTOSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentO-glycosyl compounds
Alternative Parents
Substituents
  • O-glycosyl compound
  • Disaccharide
  • C-glycosyl compound
  • Oxane
  • Tetrahydrofuran
  • Secondary alcohol
  • Hemiacetal
  • Oxacycle
  • Organoheterocyclic compound
  • Polyol
  • Acetal
  • Hydrocarbon derivative
  • Primary alcohol
  • Alcohol
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Organoleptic EffectsNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility792 g/LALOGPS
logP-3.3ALOGPS
logP-4.5ChemAxon
logS0.36ALOGPS
pKa (Strongest Acidic)10.28ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area189.53 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity68.77 m³·mol⁻¹ChemAxon
Polarizability31.48 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
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GC-MSGC-MS Spectrumsplash10-0uxr-0951000000-d976341b4e779d2fcb68Not AvailableView Spectrum
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LC-MS/MSLC-MS/MS Spectrumsplash10-03dj-1391000000-3cd7d2eb33cffdbe7c0aNot AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-0gx9-9882000000-bc1917fd2317412bcf0dNot AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-0aos-4963000000-e25ea9ff5112e9dc3878Not AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-000m-9300000000-6b498978a96b701385f8Not AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-01p9-9000000000-15b5034137e74b951824Not AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-05fr-9000000000-cf6f6d8ebcf74471e6bdNot AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-03dj-3900000000-d42735b59aac8a15dc1bNot AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-0uk9-9500000000-07a453cd3d78508e4ed7Not AvailableView Spectrum
LC-MS/MSLC-MS/MS Spectrumsplash10-0ik9-3900000000-336ba3f6ae66e534896dNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-01sl-0926000000-5535dc771cd3475f78d9Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-03e9-1901000000-7527f9131144e0052e9eNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-03di-6900000000-0593d0024a70c2c9c2c9Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0096-2759000000-a4aeb60cfb18e5e48f3bNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-01t9-1901000000-63959fadbaf2b9b31c47Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-002g-7900000000-6748915d3cd5de1f2448Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-000x-0509000000-cd75ae8f3f446217f77fNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-001j-0913000000-dd75b551be71bc37e076Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0aos-9620000000-8af907f3868b6dd93de2Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-0006-0169000000-0a76563b491714164700Not AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-004l-5964000000-fcc0a7748ac9d15133deNot AvailableView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrumsplash10-004l-9700000000-6979eb4be12c203e2727Not AvailableView Spectrum
1D NMR1H NMR Spectrum (1D, D2O, predicted)Not AvailableNot AvailableView Spectrum
1D NMR13C NMR Spectrum (1D, D2O, predicted)Not AvailableNot AvailableView Spectrum
Toxicity Profile
Mechanism of ToxicityNot Available
Carcinogenicity (IARC Classification)Not Available
Minimum Risk LevelNot Available
SymptomsNot Available
TreatmentNot Available
Toxicity Values
Toxicity ValueUnitValue RangeOrganismDose DescriptorRoute of ExposurePredicted or ExperimentalReference
12095.0Log mg/kg[6800:22000]RatLD50oralpredictedNot Available
Health Effects
Health EffectRelationshipDirectionReference
Exposure Sources
Source IDSourceSectorReference
253Drugs for constipationHealthcare, pharmaceuticals & veterinary productsNot Available
490Personal care & cosmeticsNot Available
495CeilingsBuilding & ConstructionNot Available
Pathways
2 pathways
Targets
StructureProteinUniProt IDOrganismRelationshipDetails
Click to view 3D structureType 1 fimbrin D-mannose specific adhesinP08191Escherichia coli K-12Predicted (SEA)0.700643
Click to view 3D structureLectinB4EH87Burkholderia cenocepacia (strain ATCC BAA-245 / DSM 16553 / LMG 16656/ NCTC 13227 / J2315 / CF5610) (Burkholderia cepacia (strain J2315))Predicted (SEA)0.700643
Click to view 3D structureEndo-beta-N-acetylglucosaminidaseQ9ZB22Arthrobacter protophormiaePredicted (SEA)0.389246
Gap junction beta-2 protein structureClick to view 3D structureGap junction beta-2 proteinP29033HumansPredicted (SEA)0.544945
CD44 antigen structureClick to view 3D structureCD44 antigenP16070HumansPredicted (SEA)0.544945
Click to view 3D structureCD44 antigenP15379Mus musculusPredicted (SEA)0.544945
Click to view 3D structureN-acetyllactosaminide alpha-1,3-galactosyltransferaseP50127Sus scrofaPredicted (SEA)0.856341
Click to view 3D structureAlpha-amylaseQ7M328Sus scrofa domesticusPredicted (SEA)0.544945
Galectin-3 structureClick to view 3D structureGalectin-3P17931HumansPredicted (SEA)8.79696
Click to view 3D structurePA-I galactophilic lectinQ05097Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG12228)Predicted (SEA)1.01204
Carbonic anhydrase 12 structureClick to view 3D structureCarbonic anhydrase 12O43570HumansPredicted (SEA)270.37
Click to view 3D structureCMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1P54751Mus musculusPredicted (SEA)3.26967
Carbonic anhydrase 7 structureClick to view 3D structureCarbonic anhydrase 7P43166HumansPredicted (SEA)225.996
Carbonic anhydrase 1 structureClick to view 3D structureCarbonic anhydrase 1P00915HumansPredicted (SEA)417.038
Beta-ketoacyl-[acyl-carrier-protein] synthase III structureClick to view 3D structureBeta-ketoacyl-[acyl-carrier-protein] synthase IIIP0A6R0Escherichia coli (strain K12)Predicted (SEA)0.544945
Click to view 3D structureKiller cell lectin-like receptor subfamily B member 1AP27471Rattus norvegicusPredicted (SEA)0.934191
Carbonic anhydrase 9 structureClick to view 3D structureCarbonic anhydrase 9Q16790HumansPredicted (SEA)570.868
Click to view 3D structureCytidine deaminaseP56389Mus musculusPredicted (SEA)11.9888
Gap junction alpha-1 protein structureClick to view 3D structureGap junction alpha-1 proteinP17302HumansPredicted (SEA)1.16774
Solute carrier family 28 member 3 structureClick to view 3D structureSolute carrier family 28 member 3Q9HAS3HumansPredicted (SEA)21.2528
Click to view 3D structureHuman immunodeficiency virus type 1 REVQ77Y21Human immunodeficiency virus 1Predicted (SEA)0.700643
Click to view 3D structureLysosomal alpha-glucosidaseQ6P7A9Rattus norvegicusPredicted (SEA)4.67095
Click to view 3D structureOligo-1,6-glucosidase IMA1P53051Saccharomyces cerevisiae S288cPredicted (SEA)17.3604
Click to view 3D structureSucrase-isomaltase, intestinalP23739Rattus norvegicusPredicted (SEA)6.07224
Carbonic anhydrase 2 structureClick to view 3D structureCarbonic anhydrase 2P00918HumansPredicted (SEA)1052.05
Concentrations
Not Available
External Links
DrugBank IDDB00581
HMDB IDHMDB0000740
FooDB IDFDB022215
Phenol Explorer IDNot Available
KNApSAcK IDC00053413
BiGG IDNot Available
BioCyc IDNot Available
METLIN ID916
PDB IDNot Available
Wikipedia LinkLactulose
Chemspider ID10856
ChEBI ID6359
PubChem Compound ID11333
Kegg Compound IDC07064
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References
1. https://www.ncbi.nlm.nih.gov/pubmed/?term=11020286
2. https://www.ncbi.nlm.nih.gov/pubmed/?term=12927899
3. https://www.ncbi.nlm.nih.gov/pubmed/?term=15735433
4. https://www.ncbi.nlm.nih.gov/pubmed/?term=23353997
5. https://www.ncbi.nlm.nih.gov/pubmed/?term=2432147
6. https://www.ncbi.nlm.nih.gov/pubmed/?term=25300228
7. https://www.ncbi.nlm.nih.gov/pubmed/?term=25466139
8. https://www.ncbi.nlm.nih.gov/pubmed/?term=25586470
9. https://www.ncbi.nlm.nih.gov/pubmed/?term=25700936
10. https://www.ncbi.nlm.nih.gov/pubmed/?term=25800379
11. https://www.ncbi.nlm.nih.gov/pubmed/?term=25835949
12. https://www.ncbi.nlm.nih.gov/pubmed/?term=25916046
13. https://www.ncbi.nlm.nih.gov/pubmed/?term=25935392
14. Dalev, P.; Tsoneva, P. Method for preparation of lactulose from lactose. Trudove na Nauchnoizsledovatelskiya Khimikofarmatsevtichen Institut (1982), 12 95-102.
15. Ohri SK, Somasundaram S, Koak Y, Macpherson A, Keogh BE, Taylor KM, Menzies IS, Bjarnason I: The effect of intestinal hypoperfusion on intestinal absorption and permeability during cardiopulmonary bypass. Gastroenterology. 1994 Feb;106(2):318-23.
16. Cox MA, Lewis KO, Cooper BT: Measurement of small intestinal permeability markers, lactulose, and mannitol in serum: results in celiac disease. Dig Dis Sci. 1999 Feb;44(2):402-6.
17. Spiller RC, Frost PF, Stewart JS, Bloom SR, Silk DB: Delayed postprandial plasma bile acid response in coeliac patients with slow mouth-caecum transit. Clin Sci (Lond). 1987 Feb;72(2):217-23.
18. Mortensen PB, Holtug K, Bonnen H, Clausen MR: The degradation of amino acids, proteins, and blood to short-chain fatty acids in colon is prevented by lactulose. Gastroenterology. 1990 Feb;98(2):353-60.
19. Goto K, Chew F, Torun B, Peerson JM, Brown KH: Epidemiology of altered intestinal permeability to lactulose and mannitol in Guatemalan infants. J Pediatr Gastroenterol Nutr. 1999 Mar;28(3):282-90.
20. La Brooy SJ, Male PJ, Beavis AK, Misiewicz JJ: Assessment of the reproducibility of the lactulose H2 breath test as a measure of mouth to caecum transit time. Gut. 1983 Oct;24(10):893-6.
21. Kamphues J, Tabeling R, Stuke O: [Possible interesting dietetic effects of lactulose as a feed additive in pig feed]. Dtsch Tierarztl Wochenschr. 2003 Sep;110(9):365-8.
22. Mortensen PB: The effect of oral-administered lactulose on colonic nitrogen metabolism and excretion. Hepatology. 1992 Dec;16(6):1350-6.
23. Szilagyi A, Rivard J, Fokeeff K: Improved parameters of lactose maldigestion using lactulose. Dig Dis Sci. 2001 Jul;46(7):1509-19.
24. van der Hulst RR, van Kreel BK, von Meyenfeldt MF, Brummer RJ, Arends JW, Deutz NE, Soeters PB: Glutamine and the preservation of gut integrity. Lancet. 1993 May 29;341(8857):1363-5.
25. van Berge Henegouwen GP, van der Werf SD, Ruben AT: Effect of long term lactulose ingestion on secondary bile salt metabolism in man: potential protective effect of lactulose in colonic carcinogenesis. Gut. 1987 Jun;28(6):675-80.
26. Neiko IeM, Mytnyk ZM, Holovach IIu: [Different therapeutic approaches for chronic diffuse liver lesions using ornicetil, lactulose, etimizol and corinfar]. Lik Sprava. 2002;(2):64-8.
27. Kamiya S, Nagino M, Kanazawa H, Komatsu S, Mayumi T, Takagi K, Asahara T, Nomoto K, Tanaka R, Nimura Y: The value of bile replacement during external biliary drainage: an analysis of intestinal permeability, integrity, and microflora. Ann Surg. 2004 Apr;239(4):510-7.
28. Mayo Medical Laboratories 2005 Test Catalog