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112901-68-5

112901-68-5 structure
112901-68-5 structure
  • Name: Amifostine trihydrate
  • Chemical Name: 2-(3-aminopropylamino)ethylsulfanylphosphonic acid,trihydrate
  • CAS Number: 112901-68-5
  • Molecular Formula: C5H21N2O6PS
  • Molecular Weight: 268.269
  • Catalog: API Special medicine Antidote
  • Create Date: 2018-09-20 07:16:48
  • Modify Date: 2024-01-01 19:44:50
  • Amifostine trihydrate (WR2721 trihydrate) is a broad-spectrum cytoprotective agent and a radioprotector. Amifostine trihydrate selectively protects normal tissues from damage caused by radiation and chemotherapy. Amifostine trihydrate is potent hypoxia-inducible factor-α1 (HIF-α1) and p53 inducer. Amifostine trihydrate protects cells from damage by scavenging oxygen-derived free radicals. Amifostine trihydrate reduces renal toxicity and has antiangiogenic action[1][2][3][4].

Name 2-(3-aminopropylamino)ethylsulfanylphosphonic acid,trihydrate
Synonyms S-{2-[(3-Aminopropyl)amino]ethyl} dihydrogen phosphorothioate trihydrate
MFCD00233058
UNII-M487QF2F4V
WR-2721
Anifostine trihydrate
Ethanethiol, 2-[(3-aminopropyl)amino]-, dihydrogen phosphate (ester), hydrate (1:3)
Amifostine
Amifostine trihydrate
Description Amifostine trihydrate (WR2721 trihydrate) is a broad-spectrum cytoprotective agent and a radioprotector. Amifostine trihydrate selectively protects normal tissues from damage caused by radiation and chemotherapy. Amifostine trihydrate is potent hypoxia-inducible factor-α1 (HIF-α1) and p53 inducer. Amifostine trihydrate protects cells from damage by scavenging oxygen-derived free radicals. Amifostine trihydrate reduces renal toxicity and has antiangiogenic action[1][2][3][4].
Related Catalog
References

[1]. John R Kouvaris, et al. Amifostine: the first selective-target and broad-spectrum radioprotector. Oncologist. 2007 Jun;12(6):738-47.

[2]. John R Kouvaris, et al. Amifostine: the first selective-target and broad-spectrum radioprotector. Oncologist. 2007 Jun;12(6):738-47.

[3]. D Maurici, et al. Amifostine (WR2721) restores transcriptional activity of specific p53 mutant proteins in a yeast functional assay. Oncogene. 2001 Jun 14;20(27):3533-40.

[4]. Efstathia Giannopoulou, et al. Amifostine inhibits angiogenesis in vivo. J Pharmacol Exp Ther. 2003 Feb;304(2):729-37.

[5]. Michael I Koukourakis, et al. Amifostine induces anaerobic metabolism and hypoxia-inducible factor 1 alpha. Cancer Chemother Pharmacol. 2004 Jan;53(1):8-14.

Density 1.367g/cm3
Boiling Point 441.7ºC at 760 mmHg
Molecular Formula C5H21N2O6PS
Molecular Weight 268.269
Flash Point 220.9ºC
Exact Mass 268.085785
PSA 158.38000
LogP 0.64900
Appearance powder
Vapour Pressure 4.9E-09mmHg at 25°C
Storage condition 2-8°C
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Precautionary Statements P301 + P312 + P330
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn: Harmful;
Risk Phrases R22
Safety Phrases 26-36
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS TE6491000
HS Code 2930909090
HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%