Determine the necessary mass, volume, or concentration for preparing a solution.
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Basic Description
| Synonyms | lactulose|D-Lactulose|Bifiteral|Cephulac|Chronulac|Constilac|Acilac|Cholac|Constulose|Isolactose|Lactulosum|Enulose|Generlac|Heptalac|Lactulosa|Laevolac|Laxilose|Portalac|Kristalose|Duphalac|Lactulosum [Latin]|4618-18-2|Actilax|Lattulosio|Lactulosum [INN- |
|---|---|
| Specifications & Purity | 10mM in DMSO |
| Biochemical and Physiological Mechanisms | Lactulose is a keto analogue of lactose. Primary bile acids are converted to carcinogenic secondary bile acids by colonic bacteria when the colonic pH is high. Addition of lactulose to the diet of experimental animals showed a significant fall in small in |
| Storage Temp | Store at -80°C |
| Shipped In | Ice chest + Ice pads |
| Product Description | A keto analogue of lactose. |
Product Properties
| ALogP | -4.3 |
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Associated Targets
DRD1 Tclin D(1A) dopamine receptor 0 Activities
ESR1 Tclin Estrogen receptor 0 Activities
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GABRA1 Tclin Gamma-aminobutyric acid receptor subunit alpha-1 0 Activities
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HRH3 Tclin Histamine H3 receptor 0 Activities
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KMT2A Tchem Histone-lysine N-methyltransferase 2A 0 Activities
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HDAC6 Tclin Histone deacetylase 6 0 Activities
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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities
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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities
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SLC6A2 Tclin Sodium-dependent noradrenaline transporter 0 Activities
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SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities
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SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities
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PGR Tclin Progesterone receptor 0 Activities
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PDE3A Tclin cGMP-inhibited 3',5'-cyclic phosphodiesterase A 0 Activities
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PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities
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PDE4A Tclin cAMP-specific 3',5'-cyclic phosphodiesterase 4A 0 Activities
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RGS4 Tchem Regulator of G-protein signaling 4 0 Activities
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DRD3 Tclin D(3) dopamine receptor 0 Activities
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KDR Tclin Vascular endothelial growth factor receptor 2 0 Activities
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CHRM2 Tclin Muscarinic acetylcholine receptor M2 0 Activities
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ACHE Tclin Acetylcholinesterase 0 Activities
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ABCB11 Tchem Bile salt export pump 0 Activities
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CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities
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ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities
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ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities
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AR Tclin Androgen receptor 0 Activities
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MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities
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HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities
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ADORA3 Tchem Adenosine receptor A3 0 Activities
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HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities
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TBXA2R Tclin Thromboxane A2 receptor 0 Activities
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F2 Tclin Prothrombin 0 Activities
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KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities
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OPRM1 Tclin Mu-type opioid receptor 0 Activities
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Names and Identifiers
| 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 |
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| INCHI | InChI=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 Key | JCQLYHFGKNRPGE-FCVZTGTOSA-N |
| Canonical SMILES | C(C1C(C(C(C(O1)OC2C(OC(C2O)(CO)O)CO)O)O)O)O |
| Isomeric SMILES | C([C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@@]([C@H]2O)(CO)O)CO)O)O)O)O |
| WGK Germany | 2 |
| RTECS | LS6965000 |
| PubChem CID | 11333 |
| Molecular Weight | 342.3 |
| Beilstein | 93773 |
Certificates
Certificate of Analysis(COA)
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Chemical and Physical Properties
| Sensitivity | Hygroscopic |
|---|---|
| Refractive Index | 1.45-1.47 |
| Melt Point(°C) | ~169 °C (dec.) |
Safety and Hazards(GHS)
| WGK Germany | 2 |
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| RTECS | LS6965000 |