Cyclouridine

  Cat. No.:  DC20140   Featured
Chemical Structure
3736-77-4
For research use only. We do not sell to patients.
We match the best price and quality on market.
Email:order@dcchemicals.com  sales@dcchemicals.com
Tel:+86-021-58447131
We are official vendor of:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
More than 5000 active chemicals with high quality for research!
Field of application
2,2'-Cyclouridine is a research tool for antiviral and anticancer studies.
Cas No.: 3736-77-4
Chemical Name: Cyclouridine
Synonyms: O2,2'-cyclouridine;2,2-Cyclouridine;02,2-Cycloridine;2,2-Anhydrocytidine;2,2-Anhydro-1-(b-D-Arabinofuranosyl) Uracil;2,2'-O-Cyclouridine;2,2'-Anhydro-1(B-D-arabinofuranosyl)uracil;2,2'-ANHYDRO-1(BETA-D-ARABINOFURANOSYL)URACIL;2,2'-ANHYDRO-1-(Β-D-ARABINOFURANOSYL)-URACIL;2,2'-Anhydrouridine;2,2'-Cyclouridine;O2,2′-Cyclouridine;2,2′-O-Cyclouridine;2,2-Anhydro-1(b-D-arabinofuranosyl)uracil;2,2'-O-Anhydro-(1-β-D-arabinofuranosyl)uracil;2,2'-Anhydro-1-(beta-D-arabinofuranosyl) uracil;Cyclouridine;2,2'-Anhydro-(1-Beta-D-Arabinofuranosyl)uracil;2,2;-Cyclouridine;2,2'-Anhydro(1-beta-D-arabinofuranosyl)uracil;O2,2'-Cyclouridine (VAN);NSC157148;Oc,2'-cyclouridine;2,2'Anhydrouridine;2,2' Anhydrouridine;2,2'-anhydro ur;BJE;2,2'-Anhydro-(1-Beta-D-Ribofuranosyl)uracil;2,2'-anhydro uridine;2, 2'-
SMILES: O[C@@H]1[C@@H](CO)O[C@@H](N2C=C3)[C@H]1OC2=NC3=O
Formula: C9H10N2O5
M.Wt: 226.1861
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: 2,2'-Anhydrouridine is used for anticancer and antiviral research[1].
References: [1]. Drabikowska AK, et al. Inhibitor properties of some 5-substituted uracil acyclonucleosides, and 2,2'-anhydrouridines versus uridine phosphorylase from E. coli and mammalian sources. Biochem Pharmacol. 1987 Dec 1;36(23):4125-8.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
2018-0101
Cat. No. Product name Field of application
DC31074 Isopropyl myristate Isopropyl myristate is the ester of isopropyl alcohol and myristic acid.
DC74557 PREX-in1 PREX-in1 is a specific small-molecule inhibitor of P-Rex1 and P-Rex2 Rac-GEF activity with IC50 of 4.5 uM (P-Rex1 DHPH Rac-GEF activity) in liposome-based GEF assay, inhibits P-Rex1 and P-Rex2 through their catalytic DH domain.
DC74555 GYS32661 GYS32661 (GYS 32661) is a potent Rac inhibitor capable of inhibiting both Rac1 and Rac1b, inhibited activated Rac1 with IC50 of 1.18 uM in in vitro pull-down assays.
DC74539 L557-0155 L557-0155 is a small molecule inhibitor of VSIG-8, prevents VSIG-8 binding to VISTA, promotes cytokine production and cell proliferation in PBMCs and suppresses melanoma growth.
DC74528 K284 K284 is a selective small molecule inhibitor of chitinase 3 like1 (CHI3L1) with strong binding affinity (Kd=-9.7 kcal·mol-1), inhibits lung metastasis by blocking IL-13Rα2-mediated JNK-AP-1 signals.
DC74225 YB-537 YB-537 (YB537) is a potent, highly specific quinone reductase 2 (QR2) inhibitor with IC50 of 3 nM, shows no activity against QR1 (IC50>10 uM).
DC74223 X-Neu5Ac X-Neu5Ac (sodium) is a substrate for chromogenic assay of neuraminidase activity in bacterial expression systems; with a Km of 0.89 mM for neuraminidase.
DC74218 UT-59 UT-59 is a specific inhibitor of cholesterol-sensing membrane protein Scap, binds to Scap's cholesterol-binding site, blocks SREBP activation and inhibits lipid synthesis.
DC74205 Tryptolinamide Tryptolinamide (TLAM) is a small-molecule compound that activates mitochondrial respiration in cybrids generated from patient-derived mitochondria and fibroblasts from patient-derived iPSCs, inhibits phosphofructokinase-1 (PFK1) with an ATP-uncompetitive
DC74203 TR-107 TR-107 (TR107) is a highly potent, selective and orally bioavailable small-molecule activator of the mitochondrial protease ClpP with EC50 of 140 nM, binds to purified ClpP with Kd value of 180 nM in surface plasmon resonance (SPR) measurement.
X