Weight | 83.518 g/mol |
---|---|
Formula | CH6ClNO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
593-56-6 (593-56-6)
methoxyamine · methoxylamine · methoxyamine hydrochloride
Score:
#1544 in Physics
,
#1614 in Biochemistry
,
#4622 in Chemistry
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- A new approach to the study of the base-excision repair pathway using methoxyamine. (Journal of Biological Chemistry, 1985)
- Therapeutic impact of methoxyamine: blocking repair of abasic sites in the base excision repair pathway. (Current opinion in investigational drugs, 2004)
- Methoxyamine potentiates DNA single strand breaks and double strand breaks induced by temozolomide in colon cancer cells (Mutation Research-dna Repair, 2001)
- Reaction of apurinic/apyrimidinic sites with [14C]methoxyamine: A method for the quantitative assay of AP sites in DNA (Biochimica et Biophysica Acta, 1983)
- Processing in vitro of an abasic site reacted with methoxyamine: a new assay for the detection of abasic sites formed in vivo. (Nucleic Acids Research, 1991)
- Niphatynes, methoxylamine pyridines from the marine sponge, niphates SP. (Tetrahedron Letters, 1987)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - methoxyamine
- methoxylamine
- methoxyamine hydrochloride
- O-methylhydroxylamine
-
SMILESCON.Cl
-
InChIKeyXNXVOSBNFZWHBV-UHFFFAOYSA-N
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