UCSF

ZINC00895313

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
July 28th, 2004 6 No

Popular Name: D-Glyceraldehyde D-Glyceraldehyde

Find On: PubMed — Wikipedia — Google

CAS Numbers: 26776-70-5 , 367-47-5 , 367-47-5; 453-17-8 , 453-17-8 , 497-09-6 , 56-82-6 , 62147-49-3 , 96-26-4 , [23147-59-3] , [26776-70-5] , [453-17-8]

Other Names:

(+-)-glyceraldehyde

(+-)-glyceraldehyde; 2,3-Dihydroxypropanal; 2,3-Dihydroxypropionaldehyde; Aldotriose; DL-glyceraldehyde; Glyceraldehyd; Glyceraldehyde; Glycerinaldehyd; Glycerose; Glyzerinaldehyd; alpha,beta-dihydroxypropionaldehyde; gliceraldehido; glyceraldehyde; glyce

(+/-)-2,3-dihydroxy-Propanal; (+/-)-Glyceraldehyde; 2, 3-dihydroxy-Propanal; 2,3-dihydroxy-Propionaldehyde; 2,3-Dihydroxypropanal; 2,3-dihydroxypropanal (ACD/Name 4.0); 2,3-Dihydroxypropionaldehyde; a,b-Dihydroxypropionaldehyde; alpha,beta-Dihydroxypropio

(+/-)-2,3-dihydroxy-Propanal; (+/-)-Glyceraldehyde; 2,3-Dihydroxypropanal; 2,3-Dihydroxypropionaldehyde; D-(+)-Glyceraldehyde; D-2,3-Dihydroxypropanal; D-2,3-Dihydroxypropionaldehyde; D-Aldotriose; D-Glyceraldehyde; D-Glycerose; DL-Glyceraldehyde; Dihydro

(+/-)-2,3-dihydroxy-Propanal;(+/-)-Glyceraldehyde;2,3-Dihydroxypropanal;2,3-Dihydroxypropionaldehyde;alpha,beta-Dihydroxypropionaldehyde;D-(+)-Glyceraldehyde;D-2,3-Dihydroxypropanal;D-2,3-Dihydroxypropionaldehyde;D-Aldotriose;D-Glyceraldehyde;D-Glycerose

(+/-)-2,3-dihydroxy-Propanal;(+/-)-Glyceraldehyde;2,3-Dihydroxypropanal;2,3-Dihydroxypropionaldehyde;D-(+)-Glyceraldehyde;D-2,3-Dihydroxypropanal;D-2,3-Dihydroxypropionaldehyde;D-Aldotriose;D-Glyceraldehyde;D-Glycerose;DL-Glyceraldehyde;Dihydroxypropional

(2r)-2,3-Dihydroxypropanal

(R)-2,3-Dihydroxypropanal

(r)-glyceraldehyde; 2,3-dihydroxypropanal; D-(+)-glyceraldehyde; D-2,3-dihydroxypropanal; D-2,3-dihydroxypropionaldehyde; D-aldotriose; D-Glyceraldehyde; D-glycerose; GLYCERALDEHYDE; Glyceraldehyde, D-; Propanal, 2,3-dihydroxy-, (R)-; Triose

1,3-Dihydroxy acetone

1,3-Dihydroxy-2-propanone

1,3-dihydroxy-2-Propanone dimer

1,3-Dihydroxyacetone

1,3-Dihydroxyacetone dimer

1,3-Dihydroxyacetone dimer, 97%

1,3-Dihydroxypropan-2-one

2,3-dihydroxypropanal

2,3-Dihydroxypropanal; 2,3-Dihydroxypropionaldehyde; 367-47-5; Aldotriose; C02154; Glyceraldehyde; Glycerose

2,3-Dihydroxypropanal; 2,3-Dihydroxypropionaldehyde; AI3-24475; Aldotriose; BRN 0635844; DL-GLYC; DL-Glyceraldehyde; DLG; Glyceraldehyde; Glyceraldehyde, (+-)-; Glyceric aldehyde; Glycerinaldehyde; Glycerinformal; Glycerose; Propanal, 2,3-dihydroxy-; Prop

2,3-Dihydroxypropanal; 2,3-Dihydroxypropionaldehyde; AI3-24475; BRN 0635844; DL-GLYC; DL-Glyceraldehyde; DLG; EINECS 200-290-0; EINECS 206-695-9; Glyceraldehyde; Glyceraldehyde, (+-)-; Glyceric aldehyde; Glycerinaldehyde; Glycerinformal; Glycerose; LS-721

2,5-Dihydroxy-1,4-dioxane-2,5-dimethanol

367-47-5; 453-17-8; D-(+)-glyceraldehyde; D-2,3-dihydroxypropanal; D-2,3-dihydroxypropionaldehyde; D-aldotriose; D-glyceraldehyde; D-glycerose; GLYCERALD; alpha,beta-dihydroxypropionaldehyde; glyceraldehyde

aldose

an aldose

Bis(hydroxymethyl) ketone

C00577; D-Glyceraldehyde

CHEBI:2561; CHEBI:13755; CHEBI:22305

CHEBI:387614; CHEBI:24343

CHEBI:39973; CHEBI:21025; CHEBI:4186; CHEBI:12982

Chromelin

D(+)-Glyceraldehyde

D-(+)-GLYCERALDEHYDE

D-(+)-Glyceraldehyde, tech.

D-(+)-Glyceraldehyde; (R)-2,3-Dihydroxy-propanal

D-(+)-glyceraldehyde; D-glyceraldehyde

D-(+)-Glyceraldehyde; D-Glyceraldehyde; NSC 91534; Propanal, 2,3-dihydroxy-, (R)- (9CI); Propanal, 2,3-dihydroxy-, (r)-; Triose; bmse000298

Dihydroxyacetone

Dihyxal

DL-GLYCERALDEHYDE

DL-Glyceraldehyde (Dimer), 93.0%+

DL-Glyceraldehyde (Dimer), 97.0%+

Dl-glyceraldehyde dimer

DNC008424

glyceraldehyde

L(-)-Glyceraldehyde

L-GLYCERALDEHYDE

LS-72118

MFCD00004670

MFCD00051019

MFCD00064378

MFCD00064379

MFCD00070528

NA

NSC 24343

O

OR-3434

Otan

Oxantin

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

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) -1.14 -3.19 -9.49 2 3 0 58 90.078 2 ↓

Vendor Notes

Note Type Comments Provided By
UniProt Database Links 5NTD_LUTLO; 5NTD_RHIMP; AK1BA_HUMAN; ALD1_MOUSE; ALD1_RAT; ALD2_CRIGR; ALD2_MOUSE; ALDR_BOVIN; ALDR_ENCCU; ALDR_HORVU; ALDR_HUMAN; ALDR_MOUSE; ALDR_PIG; ALDR_RABIT; ALDR_RAT; ALRA_DICDI; ALRB_DICDI; ALRC_DICDI; DHGA_ACICA; FCDH_PSESP; FUCI_BACFN; FUCI_BAC ChEBI
ALOGPS_SOLUBILITY 8.14e+02 g/l DrugBank-experimental
Purity 95% Fluorochem
UniProt Database Links A1A1A_DANRE; A1A1B_DANRE; ADHS_METJA; AHR_ECOLI; AK1A1_BOVIN; AK1A1_CHICK; AK1A1_CRIGR; AK1A1_HUMAN; AK1A1_MOUSE; AK1A1_PIG; AK1A1_PONAB; AK1A1_RAT; AK1A1_XENLA; AK1A1_XENTR; AK1BA_HUMAN; AKRC9_ARATH; AL7A1_HUMAN; ALDB_ECOLI; ALDCA_DANRE; ALDCB_DANRE; ALD ChEBI
Melting_Point ca 75-82? Alfa-Aesar
Melting_Point ca 75-82° Alfa-Aesar
Patent Database Links EP0784936; EP1669353; EP1882480; US2007254017; US2007264209; WO2005040149; WO2006034269; WO2007099432; WO2007099434; WO2007124465; WO2007127172 ChEBI
Patent Database Links EP0792643; EP0880964; EP0982306; EP1022272; EP1026149; EP1041068; EP1064964; EP1082313; EP1099440; EP1106210; EP1125580; EP1136071; EP1167357; EP1167366; EP1201649; EP1201660; EP1241176; EP1247809; EP1260224; EP1317884; EP1364957; EP1364958; EP1400529; EP ChEBI
Patent Database Links EP1894577 ChEBI
Reactome Database Links REACT_2013; REACT_52 ChEBI

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
ALDR-5-E Aldose Reductase (cluster #5 Of 5), Eukaryotic Eukaryotes 10 1.87 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
ALDR_HUMAN P15121 Aldose Reductase, Human 10 1.87 Binding ≤ 1μM
ALDR_HUMAN P15121 Aldose Reductase, Human 10 1.87 Binding ≤ 10μM

Direct Reactome Annotations (via ChEBI)

Description Species
Fructose catabolism

Reactome Annotations from Targets (via Uniprot)

Description Species
Pregnenolone biosynthesis

Analogs ( Draw Identity 99% 90% 80% 70% )

No pre-computed analogs available. Try a structural similarity search.