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Acivicin hydrochloride 是 Streptomyces sviceus 产生的天然产物
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1. The mouse bone marrow micronucleus test: evaluation of 21 drug candidates.
Upjohn Company, Kalamazoo, MI 49001.
Mutat Res (P 0027-5107 E 0027-5107) H指数:0 1989 年 223 卷 2 期 129-40 页
PMID:2525668 相似文献
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01. | Animals | 100 篇 | 98.039% |
02. | Micronucleus Tests | 90 篇 | 88.235% |
03. | Bone Marrow | 89 篇 | 87.255% |
04. | Mice | 83 篇 | 81.373% |
05. | Mutagens | 79 篇 | 77.451% |
06. | Male | 75 篇 | 73.529% |
07. | Dose-Response Relationship, Drug | 38 篇 | 37.255% |
08. | Female | 37 篇 | 36.275% |
09. | Bone Marrow Cells | 26 篇 | 25.490% |
10. | Chromosome Aberrations | 22 篇 | 21.569% |
https://pubmed.ncbi.nlm.nih.gov/2525668/
Mutat Res
. 1989 Jun;223(2):129-40.
doi: 10.1016/0165-1218(89)90041-4.
The mouse bone marrow micronucleus test: evaluation of 21 drug candidates
Affiliations expand
PMID: 2525668
Abstract
The mouse bone-marrow micronucleus test is one of the most widely used genetic toxicology assays. In this report the results of testing 21 compounds in the micronucleus test are presented. Of the 21 compounds tested, 3 potential chemotherapeutic agents were identified as strongly clastogenic. In addition, one compound was identified as a weak inducer of micronuclei in the assay. Further testing of this compound in an in vivo bone marrow metaphase analysis failed to confirm this material as clastogenic. The remaining 17 compounds were classified as negative in the assay. In general the results of the micronucleus test agreed with the results of other genetic toxicology assays on this group of compounds.
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MeSH terms
Animals
Antibiotics, Antineoplastic
Benzofurans
Bone Marrow / drug effects
Bone Marrow / ultrastructure
Cyclohexanecarboxylic Acids / toxicity
Cyclohexenes
Duocarmycins
Female
Indoles*
Isoxazoles / toxicity
Male
Menogaril
Mice
Micronucleus Tests*
Mutagens*
Nogalamycin / analogs & derivatives
Nogalamycin / toxicity
Piperazines / toxicity
Structure-Activity Relationship
Substances
Antibiotics, Antineoplastic
Benzofurans
Cyclohexanecarboxylic Acids
Cyclohexenes
Duocarmycins
Indoles
Isoxazoles
Mutagens
Piperazines
adozelesin
Menogaril
losulazine hydrochloride
Nogalamycin
acivicin
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