Etoglucid
Chemical compound
- L01AG01 (WHO)
- 2-[12-(oxiran-2-yl)-2,5,8,11-tetraoxadodecan-1-yl]oxirane
- 1954-28-5
Y
- 16058
- 15246
N
- 4F9KUA0T4D
- D07256
Y
- ChEMBL460287
N
- DTXSID80862800
![Edit this at Wikidata](http://upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png)
- Interactive image
- O(CCOCCOCC1OC1)CCOCC2OC2
InChI
- InChI=1S/C12H22O6/c1(13-3-5-15-7-11-9-17-11)2-14-4-6-16-8-12-10-18-12/h11-12H,1-10H2
N
- Key:UMILHIMHKXVDGH-UHFFFAOYSA-N
N
![☒](http://upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png)
![check](http://upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png)
Etoglucid is a drug used in chemotherapy.[1] It is an epoxide compound.[2]
References
- ^ Flamm J, Donner G, Bucher A, Höltl W, Albrecht W, Havelec L (March 1994). "[Topical immunotherapy (KLH) vs. chemotherapy (Ethoglucid) in prevention of recurrence of superficial bladder cancer. A prospective randomized study]". Urologe A (in German). 33 (2): 138–43. PMID 8178408.
- ^ PubChem. "Etoglucid". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-03-02.
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Intracellular chemotherapeutic agents / antineoplastic agents (L01)
(M phase)
Block microtubule assembly | |
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Block microtubule disassembly |
inhibitor
DNA precursors/ antimetabolites (S phase) |
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Topoisomerase inhibitors (S phase) |
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Crosslinking of DNA (CCNS) |
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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