379506
三(2,3-环氧丙基)异氰尿酸酯
别名:
1,3,5-三（环氧-2-基甲基）-1,3,5-三嗪-2,4,6-三酮, 异氰尿酸三缩水甘油酯, 甲状腺球蛋白
质量水平
SMILES字符串
O=C1N(CC2CO2)C(=O)N(CC3CO3)C(=O)N1CC4CO4
InChI
1S/C12H15N3O6/c16-10-13(1-7-4-19-7)11(17)15(3-9-6-21-9)12(18)14(10)2-8-5-20-8/h7-9H,1-6H2
InChI key
OUPZKGBUJRBPGC-UHFFFAOYSA-N
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警示用语：
Danger
危险分类
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Muta. 1B - Skin Sens. 1 - STOT RE 2
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
G Atassi et al.
Cancer treatment reviews, 11 Suppl A, 99-110 (1984-03-01)
As a follow-up to our initial results on the antineoplastic activity of alpha-1,3,5-triglycidyl-s-triazinetrione (alpha TGT, NSC-296934, Teroxirone), many new epoxyde derivatives were tested against murine tumours, mostly against P388 leukaemia, to determine their antineoplastic role and to characterize their specific
Jing-Ping Wang et al.
Toxicology and applied pharmacology, 273(1), 110-120 (2013-08-21)
In this work, we demonstrated that the growth of human non-small-cell-lung-cancer cells H460 and A549 cells can be inhibited by low concentrations of an epoxide derivative, teroxirone, in both in vitro and in vivo models. The cytotoxicity was mediated by
Occupational contact dermatitis from triglycidyl isocyanurate in a powder paint factory.
C S Munro et al.
Contact dermatitis, 26(1), 59-59 (1992-01-01)
P Dombernowsky et al.
Cancer chemotherapy and pharmacology, 11(1), 59-61 (1983-01-01)
alpha-1,3,5-Triglycidyl-s-triazinetrione (TGT) is a triepoxide derivative with alkylating properties discovered by random screening. TGT has been found to be active against a wide variety of murine tumors, including a P388 subline resistant to cyclophosphamide. The starting dose in this phase-I
J A Neidhart et al.
Cancer treatment reports, 68(9), 1115-1119 (1984-09-01)
Teroxirone is a novel triepoxide, synthesized as an alkylator and showing a broad spectrum of preclinical activity. It has good cytotoxic activity against sublines of P388 and L1210 leukemias resistant to another alkylating agent, cyclophosphamide. Thirty-six patients received teroxirone as
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