form
powder
Quality Level
SMILES string
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
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Muta. 1B - Skin Sens. 1 - STOT RE 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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
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
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 379506-100G | 04061833597224 |
| 379506-500G | 04061833597231 |


