In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 3rd, 2005 | 12 | No |
Popular Name: D-Glucose D-Glucose
Find On: PubMed — Wikipedia — Google
CAS Numbers: 105931-74-6 , 110187-42-3 , 14431-43-7 , 18991-62-3 , 201417-06-3 , 492-61-5 , 492-62-6 , 50-99-7 , 59-23-4 , 5996-10-1 , 99349-68-5 , [55324-97-5]
14431-43-7; Cartose (TN); D02325; Dextrose (USP); alpha-D-Glucose monohydrate
3-(Acrylamido)phenylboronic acid
492-62-6; C00267; alpha-D-Glucose
50-99-7; C00031; D-Glucose; Dextrose; Glucose; Grape sugar
50-99-7; D-Glucose; D00009; Glucose (JP16)
6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetraol; D-glucose; alpha-D-glucose; alpha-glucose; glucose
6-Amino-6-deoxy glucose hydrochloride
alpha-D(+)-Glucose, 99+%, anhydrous
alpha-D-Glc; alpha-D-glucose; alpha-dextrose
CARAWAY (CARUM CARVI L.); Caraway; Carum carvi; Cumin des pres; Kummel; LS-2507
CHEBI:12318; CHEBI:40557; CHEBI:42802; CHEBI:22386; CHEBI:10242
CHEBI:138; CHEBI:10809; CHEBI:18503
D(+)-Glucose monohydrate, extra pure
D(+)-Glucose, ACS reagent, anhydrous
D-Glc; D-Glcp; D-Glucose; D-glucose; Dextrose; Grape sugar; glucose
Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | -2.64 | -10.59 | -8.3 | 5 | 6 | 0 | 110 | 180.156 | 1 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
Mp [°C] | 146 | Acros Organics |
Melting_Point | 147-153? | Alfa-Aesar |
Melting_Point | 147-153° | Alfa-Aesar |
Mp [°C] | 156 - 158 | Acros Organics |
Mp [°C] | 165 - 168 | Acros Organics |
UniProt Database Links | 2AMD_PSEPS; 3AT1_ARATH; 3AT2_ARATH; 3OAGR_CLOPH; 4CGT_ANTMA; 5GT1_PERFR; 5GT2_PERFR; 5GT_GENTR; 5GT_VERHY; 5HT2C_CANFA; 5HT2C_HUMAN; 5HT2C_MOUSE; 5HT2C_PANTR; 5HT2C_RAT; 5MAT_ARATH; 5NTD_LUTLO; 5NTD_RHIMP; 6GPD3_ARATH; 6P22_YEAST; 6PGD1_ARATH; 6PGD1_ORYSJ | ChEBI |
UniProt Database Links | AGLA_THENE; AMY_BACSP; CTA1_BACCI; GLGX_ERWCH; PHSL_VICFA; SSG1B_HORVU; SSG1_ARATH; SSG1_FAGES; SSG1_HORVU; SSG1_IPOBA; SSG1_MAIZE; SSG1_MANES; SSG1_ORYGL; SSG1_ORYSA; SSG1_ORYSI; SSG1_ORYSJ; SSG1_PEA; SUSB_BACTN | ChEBI |
UniProt Database Links | AMY1_AEDAE; AMY1_AERHY; AMY1_ARATH; AMY1_BACFI; AMY1_CAPAA; AMY1_CAPCH; AMY1_DICT6; AMY1_ECOLI; AMY1_HORVU; AMY1_HUMAN; AMY1_LIPKO; AMY1_MOUSE; AMY1_ORYSJ; AMY1_SCHOC; AMY1_SCHPO; AMY2A_ORYSI; AMY2A_ORYSJ; AMY2B_HUMAN; AMY2_ARATH; AMY2_CAPCH; AMY2_DICT6 | ChEBI |
PUBCHEM_PATENT_ID | EP0130829A2; US4644085 | IBM Patent Data |
Patent Database Links | EP1061080; EP1375498; EP1527782; EP1568346; EP1568351; EP1570843; EP1589067; EP1591107; EP1598062; EP1623976; EP1629729; EP1632137; EP1639903; EP1645568; EP1674078; EP1674474; EP1719503; EP1743693; EP1752127; EP1757279; EP1767212; EP1834950; EP1834951; EP | ChEBI |
Reactome Database Links | REACT_115656; REACT_115663; REACT_115724; REACT_115737; REACT_1338; REACT_1433; REACT_163853; REACT_163926; REACT_1682; REACT_1827; REACT_19138; REACT_19288; REACT_19292; REACT_19335; REACT_19350; REACT_19399; REACT_21316; REACT_21415; REACT_23791; REACT_ | ChEBI |
S phrase | S24/25: Avoid contact with skin and eyes. | Acros Organics |
No pre-computed analogs available. Try a structural similarity search.