UCSF

ZINC03860903

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
October 3rd, 2005 12 No

Popular Name: D-Mannose D-Mannose

Find On: PubMed — Wikipedia — Google

CAS Numbers: 15572-79-9 , 31103-86-3 , 3458-28-4 , 51059-75-7 , 530-26-7

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) -2.64 -10.58 -8.84 5 6 0 110 180.156 1 ↓

Vendor Notes

Note Type Comments Provided By
Melting_Point 127-133? Alfa-Aesar
Melting_Point 127-133° Alfa-Aesar
Mp [°C] 133 Acros Organics
UniProt Database Links 14KL_BRUA1; 14KL_BRUA2; 14KL_BRUAB; 14KL_BRUC2; 14KL_BRUME; 14KL_BRUO2; 14KL_BRUSI; 14KL_BRUSU; 14KL_OCHA4; 209L2_MACMU; ACE_BOVIN; ACE_HUMAN; ACE_MESAU; ACE_MOUSE; ACE_PANTR; ACE_RABIT; ACE_RAT; ACH1_YEAST; ACYLT_MYCS2; ACYLT_MYCTU; ADPP_BACSU; ADPP_ECO5 ChEBI
UniProt Database Links ALGA_PSEAE; ALGA_PSEFL; ALGA_PSEPK; ALGA_PSESM; ALGC_PSEAE; ALGC_PSEPK; ALGC_PSESM; EDEM3_HUMAN; EDEM3_MOUSE; EDEM3_XENLA; EXOC_AZOBR; GMPAA_DANRE; GMPAA_XENLA; GMPAB_DANRE; GMPAB_XENLA; GMPBA_XENLA; GMPBB_XENLA; GMPP1_ARATH; GMPP1_ORYSJ; GMPP2_ARATH; GMP ChEBI
Reactome Database Links REACT_163764; REACT_19292; REACT_24995; REACT_25047; REACT_25093; REACT_25126; REACT_25205; REACT_25217; REACT_25313; REACT_25341 ChEBI
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
ER Quality Control Compartment (ERQC)
Na+-dependent glucose transporters
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 t
Reactions specific to the complex N-glycan synthesis pathway
Scavenging by Class A Receptors

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