Top Suppliers:I want be here

5116-24-5

5116-24-5 structure
5116-24-5 structure
  • Name: 5-Hydroxymethyl-2'-deoxyuridine
  • Chemical Name: 5-hydroxymethyl-2'-deoxyuridine
  • CAS Number: 5116-24-5
  • Molecular Formula: C10H14N2O6
  • Molecular Weight: 258.228
  • Catalog: Biochemical Nucleoside drugs Deoxynucleotides and their analogues
  • Create Date: 2018-04-01 08:00:00
  • Modify Date: 2024-01-15 08:07:03
  • 5-Hydroxymethyl-2'-deoxyuridine is a nucleoside analog. 5-Hydroxymethyl-2'-deoxyuridine inhibits the replication of multiple human leukemia cell lines with IC50 values of 1.7-5.8 μM. 5-Hydroxymethyl-2'-deoxyuridine prolongs the survival of mice carrying L1210 leukemia. 5-Hydroxymethyl-2'-deoxyuridine can be used for the research of cell replication and leukemia[1][2][3].

Name 5-hydroxymethyl-2'-deoxyuridine
Synonyms 1-(2-Deoxypentofuranosyl)-5-(hydroxymethyl)-2,4(1H,3H)-pyrimidinedione
2,4(1H,3H)-Pyrimidinedione, 1-(2-deoxypentofuranosyl)-5-(hydroxymethyl)-
5-HMdU HMdUdr
1-(2-deoxypentofuranosyl)-5-(hydroxymethyl)pyrimidine-2,4(1H,3H)-dione
5-HYDROXYMETHYL-2'-DEOXYURIDINE
Description 5-Hydroxymethyl-2'-deoxyuridine is a nucleoside analog. 5-Hydroxymethyl-2'-deoxyuridine inhibits the replication of multiple human leukemia cell lines with IC50 values of 1.7-5.8 μM. 5-Hydroxymethyl-2'-deoxyuridine prolongs the survival of mice carrying L1210 leukemia. 5-Hydroxymethyl-2'-deoxyuridine can be used for the research of cell replication and leukemia[1][2][3].
Related Catalog
In Vitro 5-Hydroxymethyl-2'-deoxyuridine (0-10 μM) inhibits the replication of Sarcoma 180 cells and Ehrlich ascites carcinoma cells with ED50 values of 8.5 and 4 μM, respectively[1]. 5-Hydroxymethyl-2'-deoxyuridine inhibits herpes simplex virus type 1 (HSV-1) pyrimidine 2’-deoxyribonucleoside kinase with a Ki value of 3.5 μM[1]. 5-Hydroxymethyl-2'-deoxyuridine inhibits the replication of multiple human leukemia cell lines with IC50 values of 1.7-5.8 μM[2]. 5-Hydroxymethyl-2'-deoxyuridine (10-100 μM) shows dose-dependent toxicity against a human acute promyelocytic leukemia cell line[2].
In Vivo 5-Hydroxymethyl-2'-deoxyuridine (0, 5 and 50 mg/kg; i.p.; once) increases the survival of DBA/2 mice carrying L1210 leukemia[3].
Density 1.6±0.1 g/cm3
Boiling Point 401.48°C (rough estimate)
Melting Point 176-179 °C
Molecular Formula C10H14N2O6
Molecular Weight 258.228
Exact Mass 258.085175
PSA 124.78000
LogP -1.49
Index of Refraction 1.610
Storage condition −20°C

CHEMICAL IDENTIFICATION

RTECS NUMBER :
YU7600000
CHEMICAL NAME :
Uridine, 2'-deoxy-5-(hydroxymethyl)-
CAS REGISTRY NUMBER :
5116-24-5
LAST UPDATED :
199709
DATA ITEMS CITED :
8
MOLECULAR FORMULA :
C10-H14-N2-O6
MOLECULAR WEIGHT :
258.26

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
3 gm/kg/15D-I
TOXIC EFFECTS :
Gastrointestinal - other changes Related to Chronic Data - death

MUTATION DATA

TYPE OF TEST :
Mutation in mammalian somatic cells
TEST SYSTEM :
Rodent - hamster Ovary
DOSE/DURATION :
4 umol/L
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 373,125,1997
Risk Phrases 24/25
Safety Phrases 24/25
WGK Germany 3
RTECS YU7600000
HS Code 2934999090
HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%