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Related CAS#:

1818-71-9

1818-71-9 structure
1818-71-9 structure
  • Name: Crotonoside
  • Chemical Name: 2-hydroxyadenosine
  • CAS Number: 1818-71-9
  • Molecular Formula: C10H13N5O5
  • Molecular Weight: 283.241
  • Catalog: Biochemical Plant extracts
  • Create Date: 2018-08-07 23:17:08
  • Modify Date: 2024-01-03 15:37:08
  • Crotonoside is isolated from Chinese medicinal herb, Croton. Crotonoside inhibits FLT3 and HDAC3/6, exhibits selective inhibition in acute myeloid leukemia (AML) cells. Crotonoside could be a promising new lead compound for the treatment of AML[1].

Name 2-hydroxyadenosine
Synonyms 3-Hydroadenosine, 2-oxo-
iso-Gr
Isoguanosine
2(1H)-Oxoadenosine
adenosine, 2-oxo-
2-Oxo-1,2-dihydro-adenosin
ISOGUANOSINE RIBOSIDE
2-Oxoadenosine
2-Oxo-3-hydroadenosine
2-Hydroxyadenosine
CROTONOSID
isoguanineriboside
CROTONOSIDE
ISOGUANOSINE(P)
Description Crotonoside is isolated from Chinese medicinal herb, Croton. Crotonoside inhibits FLT3 and HDAC3/6, exhibits selective inhibition in acute myeloid leukemia (AML) cells. Crotonoside could be a promising new lead compound for the treatment of AML[1].
Related Catalog
Target

FLT3

HDAC3

HDAC6

In Vitro Crotonoside (0-200 μM;) selectively inhibits the viability of AML cell line MV4-11, MOLM-13 (with FLT3-ITD mutant) and KG-1 (without FLT3-ITD mutant) in a dose-dependent manner with an IC50 of 11.6 μM, 12.7 μM and 17.2 μM, respectively[1]. Crotonoside (0-100μM; 7 hours) inhibits the phosphorylation of FLT3 Erk1/2, Akt/mTOR and STAT5 is strongly inhibited by crotonoside at higher concentration of 12.5 μM in a concentration-dependent manner[1]. Crotonoside (0-100 μM; 12 hours) exhibits a dose-dependent increase in the percentage of G0/G1 phase and a dose-dependent decrease in the percentage of G2/M and S phases cells[1]. Crotonoside (0-100 μM; 24 hours) leads to concentration-dependent changes in the number of apoptotic MV4-11 cells, results in a dose-dependent decrease in the level of pro-caspase-3 and a dose-dependent increase in the level of the cleaved caspase-3 fragments[1]. Cell Viability Assay[1] Cell Line: AML cell line MV4-11, MOLM-13 and KG-1 cells Concentration: 0-200 μM Incubation Time: 72 hours Result: Inhibited AML cells growth than other cell lines tested. Western Blot Analysis[1] Cell Line: MV4-11 cells Concentration: 0 μM, 12.5 μM, 25 μM, 50 μM Incubation Time: 7 hours Result: Inhibited AML cells growth than other cell lines tested. Cell Cycle Analysis[1] Cell Line: MV4-11 cells Concentration: 0 μM, 12.5 μM, 25 μM, 50 μM Incubation Time: 12 hours Result: Induced cell cycle arrest in G0/G1. Apoptosis Analysis[1] Cell Line: MV4-11 cells Concentration: 0 μM, 12.5 μM, 25 μM, 50 μM Incubation Time: 24 hours Result: Induced MV4-11 cell apoptosis.
In Vivo Crotonoside(intraperitoneal and intravenous injection; 70 mg/kg, 35 mg/kg; once daily) induces a significant antitumor activity and inhibited xenograft tumor progress as compared to treatment with vehicle[1]. Animal Model: NOD-SCID mice with MV4-11 cells[1] Dosage: 70 mg/kg, 35 mg/kg Administration: Intraperitoneal and intravenous injection; 70 mg/kg, 35 mg/kg; once daily Result: Produced significant AML tumor inhibition rates of 93.5% at 70 mg/kg.
References

[1]. Li YZ,et al. Crotonoside exhibits selective post-inhibition effect in AML cells via inhibition of FLT3 and HDAC3/6. Oncotarget. 2017 Sep 8;8(61):103087-103099.

Density 2.3±0.1 g/cm3
Boiling Point 831ºC at 760 mmHg
Molecular Formula C10H13N5O5
Molecular Weight 283.241
Flash Point 456.4ºC
Exact Mass 283.091675
PSA 159.51000
LogP -3.42
Vapour Pressure 2.83E-29mmHg at 25°C
Index of Refraction 1.955
Hazard Codes Xi
Safety Phrases 24/25
RIDADR NONH for all modes of transport
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%