MedKoo Cat#: 462702 | Name: SR 2555

Description:

WARNING: This product is for research use only, not for human or veterinary use.

SR 2555 is a biochemical with tumor and neural tissue penetrating properties.

Chemical Structure

SR 2555
SR 2555
CAS#74141-74-5

Theoretical Analysis

MedKoo Cat#: 462702

Name: SR 2555

CAS#: 74141-74-5

Chemical Formula: C9H14N4O5

Exact Mass: 258.0964

Molecular Weight: 258.23

Elemental Analysis: C, 41.86; H, 5.46; N, 21.70; O, 30.98

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
NSC 314055; NSC314055; NSC-314055;
IUPAC/Chemical Name
N,N-bis(2-hydroxyethyl)-2-(2-nitro-1H-imidazol-1-yl)acetamide
InChi Key
KGFGBSRVWKBWIC-UHFFFAOYSA-N
InChi Code
InChI=1S/C9H14N4O5/c14-5-3-11(4-6-15)8(16)7-12-2-1-10-9(12)13(17)18/h1-2,14-15H,3-7H2
SMILES Code
OCCN(C(Cn1c([N+]([O-])=O)ncc1)=O)CCO
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 258.23 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: White RA, Workman P, Brown JM. The pharmacokinetics and tumor and neural tissue penetrating properties of SR-2508 and SR-2555 in the dog--hydrophilic radiosensitizers potentially less toxic than misonidazole. Radiat Res. 1980 Dec;84(3):542-61. PMID: 6450431. 2: Rootman J, Gallie B, Kumi C, Bussanich N, Rogers B, Palcic B. Ocular penetration, toxicity, and radiosensitization effects of two hypoxic cell radiosensitizers on retinoblastoma. Arch Ophthalmol. 1986 Nov;104(11):1693-7. doi: 10.1001/archopht.1986.01050230131048. PMID: 2946282. 3: Workman P, Brown JM. Structure-pharmacokinetic relationships for misonidazole analogues in mice. Cancer Chemother Pharmacol. 1981;6(1):39-49. doi: 10.1007/BF00253009. PMID: 7273265. 4: Workman P. Pharmacokinetics of hypoxic cell radiosensitizers: a review. Cancer Clin Trials. 1980 Fall;3(3):237-51. PMID: 7438321. 5: Moldenhauer H, Rose H, Saul G, Wolf G, Kehrberg G. Die Verstärkung der Zytostatikawirkung durch Radiosensitizer--eine Ubersicht zum gegenwärtigen Stand der Chemosensibilisierung [Intensification of cytostatic action by radiosensitizers--a review of the present status of chemosensitization]. Radiobiol Radiother (Berl). 1984;25(2):289-95. German. PMID: 6234615. 6: Sutherland RM, Keng P, Conroy PJ, McDermott D, Bareham BJ, Passalacqua W. In vitro hypoxic cytotoxicity of nitroimidazoles: uptake and cell cycle phase specificity. Int J Radiat Oncol Biol Phys. 1982 Mar-Apr;8(3-4):745-8. doi: 10.1016/0360-3016(82)90726-x. PMID: 7107409. 7: Hirst DG, Hazlehurst JL, Brown JM. Sensitization of normal and malignant tissue to cyclophosphamide by nitroimidazoles with different partition coefficients. Br J Cancer. 1984 Jan;49(1):33-42. doi: 10.1038/bjc.1984.6. PMID: 6229264; PMCID: PMC1976681. 8: Brown JM, Yu NY, Brown DM, Lee WW. SR-2508: a 2-nitroimidazole amide which should be superior to misonidazole as a radiosensitizer for clinical use. Int J Radiat Oncol Biol Phys. 1981 Jun;7(6):695-703. doi: 10.1016/0360-3016(81)90460-0. PMID: 6457018. 9: Astor M, Hall EJ, Biaglow JE, Parham JC. Newly synthesized hypoxia-mediated drugs as radiosensitizers and cytotoxic agents. Int J Radiat Oncol Biol Phys. 1982 Jan;8(1):75-83. doi: 10.1016/0360-3016(82)90388-1. PMID: 7061257. 10: Shrieve DC, Harris JW. The in vitro sensitivity of chronically hypoxic EMT6/SF cells to X-radiation and hypoxic cell radiosensitizers. Int J Radiat Biol Relat Stud Phys Chem Med. 1985 Jul;48(1):127-38. doi: 10.1080/09553008514551131. PMID: 3159699. 11: Siemann DW. Response of murine tumours to combinations of CCNU with misonidazole and other radiation sensitizers. Br J Cancer. 1982 Feb;45(2):272-81. doi: 10.1038/bjc.1982.43. PMID: 6460517; PMCID: PMC2010911. 12: Hall EJ. Oncogenic transformation systems involving mammalian cells in vitro to determine the relative risks of different treatment modalities. Strahlentherapie. 1984 Dec;160(12):725-31. PMID: 6515665. 13: Brown JM, Yu NY. The optimum time for irradiation relative to tumour concentration of hypoxic cell sensitizers. Br J Radiol. 1980 Sep;53(633):915-6. doi: 10.1259/0007-1285-53-633-915. PMID: 7437721.