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EC number: 276-957-5 | CAS number: 72869-86-4
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Genetic toxicity: in vitro
Administrative data
- Endpoint:
- in vitro gene mutation study in bacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 27 May - 25 June 2009
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Version / remarks:
- 1997
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
- Version / remarks:
- 2008
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Landesamt für Umwelt, Wasserwirtschaft und Gewerbeaufsicht, Mainz, Germany
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- 7,7,9(or 7,9,9)-trimethyl-4,13-dioxo-3,14-dioxa-5,12-diazahexadecane-1,16-diyl bismethacrylate
- EC Number:
- 276-957-5
- EC Name:
- 7,7,9(or 7,9,9)-trimethyl-4,13-dioxo-3,14-dioxa-5,12-diazahexadecane-1,16-diyl bismethacrylate
- Cas Number:
- 72869-86-4
- Molecular formula:
- C23H38N2O8
- IUPAC Name:
- 2-[({2,2,4-trimethyl-6-[({2-[(2-methylprop-2-enoyl)oxy]ethoxy}carbonyl)amino]hexyl}carbamoyl)oxy]ethyl 2-methylprop-2-enoate; 2-[({2,4,4-trimethyl-6-[({2-[(2-methylprop-2-enoyl)oxy]ethoxy}carbonyl)amino]hexyl}carbamoyl)oxy]ethyl 2-methylprop-2-enoate
Constituent 1
Method
- Target gene:
- his operon (for S. typhimurium strains)
Species / strain
- Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and TA 102
- Metabolic activation:
- with and without
- Metabolic activation system:
- co-factor supplemented post-mitochondrial fraction (S9 mix), prepared from the livers of rats treated with Aroclor 1254
- Test concentrations with justification for top dose:
- First experiment: 50, 150, 500, 1501 and 5004 µg/plate with and without metabolic activation
Second experiment: 312, 624, 1247, 2493 and 4986 µg/plate with and without metabolic activation - Vehicle / solvent:
- - Vehicle/solvent used: DMSO
- Justification for choice of solvent/vehicle: DMSO was chosen because the test substance was completely soluble, and this solvent does not have any effects on the viability of the bacteria or the number of spontaneous revertants.
Controls
- Untreated negative controls:
- yes
- Remarks:
- water
- Negative solvent / vehicle controls:
- yes
- Remarks:
- DMSO
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- sodium azide
- benzo(a)pyrene
- other: 4-Nitro-1,2-phenylene diamine (4-NPD); 2-Amino-Anthracene (2-AA)
- Remarks:
- +S9: 2-AA (1 µg/plate, TA100, TA102, TA1535, TA97a); B[a]P (20 µg/plate, TA98); -S9: sodium azide (1 µg/plate, TA100 and TA1535); 4-NPD (20 µg/plate, TA102, TA97a, TA98)
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in agar (plate incorporation) (experiment 1); preincubation (experiment 2)
DURATION
- Preincubation period: 20 min
- Exposure duration: 48 h
NUMBER OF REPLICATIONS: quadruplicates each in 2 independent experiment
DETERMINATION OF CYTOTOXICITY
- Method: reduction in the number of spontaneous revertants or a clearing of the bacterial background lawn - Evaluation criteria:
- A test substance is considered to have a mutagenic potential if a significant, reproducible increase of revertant colonies per plate (increase factor ≥ 2) in at least one strain can be observed. A concentration-related increase over the range tested can also be taken as a sign of mutagenic activity.
- Statistics:
- Mean values, standard deviations and the increase factor of revertant induction were calculated.
Results and discussion
Test results
- Species / strain:
- S. typhimurium, other: TA97a, TA98, TA100, TA102 and TA1535
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Remarks:
- but tested up to limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Additional information on results:
- COMPARISON WITH HISTORICAL CONTROL DATA: The determined values for the spontaneous revertants of the negative controls and all positive control values were in the range of historical data.
Any other information on results incl. tables
Table 1. Test results of Experiment 1 (plate incorporation)
With or without S9 mix |
Test substance concentration [μg/plate] |
Mean number of revertant colonies per plate (average of 4 plates ± standard deviation) |
||||
Base-pair substitution type |
Frameshift type |
|||||
TA 100 |
TA102 |
TA1535 |
TA97a |
TA98 |
||
- |
0 (H2O) |
110 ± 12.0 |
264 ± 47.0 |
6 ± 1.9 |
105 ± 4.2 |
7 ± 1.4 |
- |
0 (DMSO) |
97 ± 6.8 |
296 ± 21.6 |
6 ± 2.1 |
96 ± 13.4 |
10 ± 1.0 |
- |
50 |
97 ± 14 |
307 ± 7 |
6 ± 1 |
104 ± 21 |
4 ± 1 |
- |
150 |
96 ± 17 |
310 ± 25 |
6 ± 1 |
105 ± 2 |
7 ± 3 |
- |
500 |
102 ± 9 |
315 ± 14 |
7 ± 4 |
89 ± 18 |
7 ± 1 |
- |
1501 |
108 ± 1 |
268 ± 36 |
8 ± 3 |
107 ± 5 |
7 ± 4 |
- |
5004 |
99 ± 10 |
275 ± 49 |
6 ± 2 |
92 ± 6 |
7 ± 3 |
Positive controls, |
Name |
NaN3 |
4-NPD |
NaN3 |
4-NPD |
4-NPD |
Concentrations [μg/plate] |
1 |
20 |
1 |
20 |
20 |
|
Mean No. of colonies/plate (average of 4 ± SD) |
630 ± 44 |
1285 ± 185 |
374 ± 18 |
445 ± 35 |
278 ± 56 |
|
+ |
0 (H2O) |
101 ± 15.8 |
345 ± 20.0 |
7 ± 1.5 |
97 ± 16.7 |
5 ± 2.8 |
+ |
0 (DMSO) |
108 ± 0.8 |
305 ± 51.7 |
9 ± 4.2 |
90 ± 13.3 |
7 ± 3.1 |
+ |
50 |
107 ± 2 |
304 ± 21 |
6 ± 3 |
109 ± 3 |
6 ± 1 |
+ |
150 |
109 ± 3 |
276 ± 33 |
7 ± 3 |
109 ± 7 |
6 ± 1 |
+ |
500 |
100 ± 6 |
309 ± 17 |
8 ± 3 |
111 ± 10 |
8 ± 2 |
+ |
1501 |
94 ± 15 |
315 ± 59 |
4 ± 2 |
99 ± 15 |
6 ± 2 |
+ |
5004 |
118 ± 21 |
330 ± 40 |
13 ± 4 |
96 ± 15 |
7 ± 2 |
Positive controls, +S9 mix |
Name |
2-AA |
2-AA |
2-AA |
2-AA |
B[a]P |
Concentrations [μg/plate] |
1 |
1 |
1 |
1 |
20 |
|
Mean No. of colonies/plate (average of 4 ± SD) |
524 ± 102 |
1093 ± 53 |
105 ± 12 |
319 ± 22 |
99 ± 9 |
NaN3: Sodium azide
4-NPD: 4-Nitro-1,2-phenylene diamine
2-AA: 2-aminoanthracene
B[a]P: Benzo-a-pyrene
Table 2. Test results of Experiment 2 (preincubation)
With or without S9 mix |
Test substance concentration [μg/plate] |
Mean number of revertant colonies per plate (average of 4 plates ± standard deviation) |
||||
Base-pair substitution type |
Frameshift type |
|||||
TA 100 |
TA102 |
TA1535 |
TA97a |
TA98 |
||
- |
0 (H2O) |
121 ± 10.0 |
299 ± 52.4 |
12 ± 3.2 |
103 ± 4.1 |
10 ± 0.0 |
- |
0 (DMSO) |
93 ± 7.1 |
274 ± 45.0 |
12 ± 1.9 |
110 ± 9.0 |
10 ± 3.7 |
- |
312 |
106 ± 12 |
282 ± 22 |
8 ± 5 |
92 ± 14 |
11 ± 6 |
- |
624 |
91 ± 9 |
232 ± 16 |
7 ± 1 |
110 ± 19 |
11 ± 2 |
- |
1247 |
110 ± 30 |
255 ± 46 |
4 ± 4 |
109 ± 10 |
10 ± 3 |
- |
2493 |
124 ± 12 |
192 ± 9 |
8 ± 3 |
114 ± 11 |
13 ± 4 |
- |
4986 |
100 ± 7 |
188 ± 18 |
9 ± 6 |
98 ± 9 |
10 ± 2 |
Positive controls, |
Name |
NaN3 |
4-NPD |
NaN3 |
4-NPD |
4-NPD |
Concentrations [μg/plate] |
1 |
20 |
1 |
20 |
20 |
|
Mean No. of colonies/plate (average of 4 ± SD) |
386 ± 37 |
1127 ± 178 |
316 ± 17 |
903 ± 73 |
978 ± 72 |
|
+ |
0 (H2O) |
97 ± 10.9 |
217 ± 12.9 |
10 ± 3.0 |
98 ± 7.4 |
14 ± 3.4 |
+ |
0 (DMSO) |
109 ± 18.1 |
290 ± 30.2 |
10 ± 3.4 |
111 ± 2.1 |
11 ± 2.6 |
+ |
312 |
109 ± 8 |
279 ± 34 |
8 ± 2 |
94 ± 10 |
11 ± 2 |
+ |
624 |
106 ± 7 |
220 ± 15 |
5 ± 3 |
104 ± 7 |
11 ± 2 |
+ |
1247 |
101 ± 10 |
218 ± 21 |
12 ± 2 |
104 ± 9 |
13 ± 3 |
+ |
2493 |
95 ± 3 |
250 ± 51 |
10 ± 6 |
102 ± 3 |
11 ± 3 |
+ |
4986 |
92 ± 6 |
235 ± 29 |
8 ± 2 |
103 ± 4 |
7 ± 2 |
Positive controls, +S9 mix |
Name |
2-AA |
2-AA |
2-AA |
2-AA |
B[a]P |
Concentrations [μg/plate] |
1 |
1 |
1 |
1 |
20 |
|
Mean No. of colonies/plate (average of 4 ± SD) |
499 ± 34 |
1345 ± 115 |
124 ± 12 |
826 ± 63 |
50 ± 5 |
NaN3: Sodium azide
4-NPD: 4-Nitro-1,2-phenylene diamine
2-AA: 2-aminoanthracene
B[a]P: Benzo-a-pyrene
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