UCSF

ZINC02583633

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
October 27th, 2004 17 Yes

Popular Name: Uridine Uridine

Find On: PubMed — Wikipedia — Google

CAS Numbers: 3083-77-0 , 54-23-9 , 58-96-8 , [58-96-8]

Other Names:

"1-(¦Â-D-Arabinofuranosyl)uracil, 98%"

"Uridine, 99%"

1-b-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione; 1-b-D-Ribofuranosyluracil; 1-beta-delta-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione; 1-beta-delta-Ribofuranosyluracil; b-D-Ribofuranoside 2,4(1H,3H)-pyrimidinedione-1; b-Uridine; beta-delta-Ribofuranoside 2,4(1

1-b-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione; 1-b-D-Ribofuranosyluracil; 1-beta-delta-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione; 1-beta-delta-Ribofuranosyluracil; Uridin; b-D-Ribofuranoside 2,4(1H,3H)-pyrimidinedione-1; b-Uridine; beta-Uridine; beta-delt

1-b-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione;1-b-D-Ribofuranosyluracil;1-beta-delta-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione;1-beta-delta-Ribofuranosyluracil;b-D-Ribofuranoside 2,4(1H,3H)-pyrimidinedione-1;b-Uridine;beta-delta-Ribofuranoside 2,4(1H,3H)-

1-b-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione;1-b-D-Ribofuranosyluracil;1-beta-delta-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione;1-beta-delta-Ribofuranosyluracil;Uridin;b-D-Ribofuranoside 2,4(1H,3H)-pyrimidinedione-1;b-Uridine;beta-Uridine;beta-delta-Ribofu

1-beta-D-Arabinofuranosyluracil

1-beta-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione; 1-beta-D-ribofuranosyluracil; Urd; Uridin; beta-Uridine; u; uridine

1-beta-D-Ribofuranosyluracil

1-beta-D-Ribofuranosyluracil; AI3-52690; C9H12N2O6; EINECS 200-407-5; LS-158705; NSC 20256; Uracil riboside; Uracil, 1-beta-D-ribofuranosyl-; Urd; Uridin; Uridine

1-beta-D-Ribofuranosyluracil; AI3-52690; URIDINE; Uracil riboside; Uracil, 1-beta-D-ribofuranosyl-; Urd; Uridin; bmse000158

1-beta-D-Ribofuranosyluracil; URIDINE; Uracil riboside; Uracil, 1-beta-D-ribofuranosyl-; Urd; Uridin; bmse000816

1-beta-D-Ribofuranosyluracil; URIDINE; Uracil riboside; Uracil, 1-beta-D-ribofuranosyl-; Urd; Uridin; bmse000864

1-[3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2,4(1H,3H)-pyrimidinedione

58-96-8; C00299; Uridine

58-96-8; uridine

Arabinofuranosyluracil

cannot calculate

CHEBI:46391; CHEBI:46386; CHEBI:46460; CHEBI:46463; CHEBI:15296; CHEBI:9893; CHEBI:27227

MFCD00006526

MFCD00065998

MFCD00079629

N/A

Uracil-1-beta-D-ribofuranoside

Uridin

Uridine, 99%

Uridine-2-14c

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) -2.09 -6.53 -15.49 4 8 0 125 244.203 2 ↓

Vendor Notes

Note Type Comments Provided By
Mp [°C] 162 - 170 Acros Organics
MP 163-167° Matrix Scientific
MP 163° Oakwood Chemical
MP 165 TCI
Melting_Point 166-169? Alfa-Aesar
Melting_Point 166-169° Alfa-Aesar
UniProt Database Links 5NT3A_HUMAN; 5NTD_LUTLO; 5NTD_RHIMP; ABC3A_HUMAN; ABC3B_HUMAN; ABC3C_GORGO; ABC3C_HUMAN; ABC3D_HUMAN; ABC3F_HUMAN; ABC3H_HUMAN; ABC3H_MACMU; ABC3H_PONPY; ABEC3_CRILO; ABEC3_MOUSE; ABEC3_RAT; ACSA1_GLUHA; ACSA1_GLUXY; AGO1_ARATH; AGO3_DROME; ALKB8_BOVIN; A ChEBI
Purity 95+% Matrix Scientific
Purity 98% APIChem
Purity 99% Fluorochem
mechanism Antimetabolite IBScreen Bioactives
Target DNA/RNA Synthesis Selleck Chemicals
PUBCHEM_PATENT_ID EP0747389A1; US5763418 IBM Patent Data
Patent Database Links EP1364957; EP1364958; EP1400529; EP1498101; EP1544208; EP1548024; EP1550668; EP1577317; EP1580188; EP1593684; EP1609798; EP1634951; EP1637539; EP1640452; EP1666092; EP1671618; EP1674104; EP1721904; EP1724277; EP1724278; EP1731155; EP1731524; EP1762611; EP ChEBI
Warnings IRRITANT Matrix Scientific
Reactome Database Links REACT_1054; REACT_1172; REACT_1236; REACT_1268; REACT_1389; REACT_1504; REACT_1812; REACT_2011; REACT_2062; REACT_2162; REACT_2200; REACT_22212; REACT_22395; REACT_358; REACT_376; REACT_714; REACT_806; REACT_958; REACT_982 ChEBI
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics
biological_use Virucide IBScreen Bioactives

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Pyrimidine catabolism
Pyrimidine salvage reactions
Transport of nucleosides and free purine and pyrimidine bases across the plasma

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