# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA658283 | F | Inhibitory concentration against camptothecin (CPT) resistant cell line using tetrazolium dye reduction assay (MTT) | Homo sapiens | 7 | cell-based format | Scientific Literature | ||
2. | ALA690466 | F | In vitro cytotoxic activity against human HT-29 cell line of colorectal carcinoma | Homo sapiens | 17 | cell-based format | Scientific Literature | ||
3. | ALA695906 | F | Inhibitory concentration against human NPC cancer cell line using tetrazolium dye reduction assay (MTT) | Homo sapiens | 7 | cell-based format | Scientific Literature | ||
4. | ALA699885 | F | Compound was tested for cell arrest at G2/M phase at 100 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
5. | ALA700037 | F | Compound was tested for cell arrest at G2/M phase at 25 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
6. | ALA700038 | F | Compound was tested for cell arrest at G2/M phase at 50 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
7. | ALA872061 | F | Compound was tested for cell arrest at Go/G1 phase at 100 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
8. | ALA700039 | F | Compound was tested for cell arrest at Go/G1 phase at 25 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
9. | ALA700040 | F | Compound was tested for cell arrest at Go/G1 phase at 50 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
10. | ALA700041 | F | Compound was tested for cell arrest at S phase at 100 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
11. | ALA700042 | F | Compound was tested for cell arrest at S phase at 25 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
12. | ALA879045 | F | Compound was tested for cell arrest at S phase at 50 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
13. | ALA700043 | F | Compound was tested for cell arrest at sub-G1 phase at 100 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
14. | ALA700044 | F | Compound was tested for cell arrest at sub-G1 phase at 25 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
15. | ALA700045 | F | Compound was tested for cell arrest at sub-G1 phase at 50 nM concentration in KB human cancer cells | Homo sapiens | 4 | cell-based format | Scientific Literature | ||
16. | ALA701766 | F | Inhibitory concentration against camptothecin (CPT) resistant cell line (KB-100) using tetrazolium dye reduction assay (MTT) | Homo sapiens | 7 | cell-based format | Scientific Literature | ||
17. | ALA702648 | F | Inhibitory concentration against VP16 resistant cell line (KB-7D) using tetrazolium dye reduction assay (MTT) | Homo sapiens | 7 | cell-based format | Scientific Literature | ||
18. | ALA873232 | F | Inhibitory concentration against vincristine-resistant cell line (KB-Vin 10) using tetrazolium dye reduction assay (MTT) | Homo sapiens | 7 | cell-based format | Scientific Literature | ||
19. | ALA704649 | F | In vitro cytotoxic activity against human KB-VIN10 cell line overexpressing P-gp 170/MDR | Homo sapiens | 17 | cell-based format | Scientific Literature | ||
20. | ALA702199 | F | Inhibitory concentration against taxol resistant cell line (KBs5) at a concentration of 50 nM using tetrazolium dye reduction assay (MTT) | Homo sapiens | 7 | cell-based format | Scientific Literature |