Assays
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# | ChEMBL ID | Assay Type | Description | Organism | Compounds | Document ChEMBL ID | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. |
F
|
Induction of ABCC2 mRNA expression in human LS180 cells at 0.1 to 1 umol/liter after 4 days by RT-PCR analysis
|
Homo sapiens
|
cell-based format
|
Scientific Literature
| ||||
2. |
P
|
Solubility of the compound
|
---
|
small-molecule physicochemical format
|
Scientific Literature
| ||||
3. |
A
|
Trough drug concentration at 12 hrs in healthy human plasma at 200 mg, po twice a day for 4 days coadministered with 400 mg of raltegravir, po twice a day for 4 days by reverse-phase HPLC-MS method
|
Homo sapiens
|
organism-based format
|
Scientific Literature
| ||||
4. |
A
|
AUC (0 to 12 hrs) in healthy human plasma at 200 mg, po twice a day for 4 days coadministered with 400 mg of raltegravir, po twice a day for 4 days by reverse-phase HPLC-MS method
|
Homo sapiens
|
organism-based format
|
Scientific Literature
| ||||
5. |
T
|
Sub-acute toxicity in Kunming mouse assessed as increase in alveolar hemorrhage administered for 14 days measured on day 14 by HE-staining based assay
|
Mus musculus
|
assay format
|
Scientific Literature
| ||||
6. |
A
|
Tmax in healthy human plasma at 200 mg, po twice a day for 8 days by reverse-phase HPLC-MS method
|
Homo sapiens
|
organism-based format
|
Scientific Literature
| ||||
7. |
F
|
Inhibition of slow delayed inward rectifying potassium current (Iks) in Chinese Hamster Ovary (CHO) cells expressing hKvLQT1/hminK measured using IonWorks Quattro automated patch clamp platform
|
Cricetulus griseus
|
cell-based format
|
Scientific Literature
| ||||
8. |
F
|
Inhibition of rapid delayed inward rectifying potassium current (IKr) in Chinese hamster ovary (CHO) K1 cells stably expressing hERG measured using IonWorks Quattro automated patch clamp platform
|
Cricetulus griseus
|
cell-based format
|
Scientific Literature
| ||||
9. |
F
|
Antiviral activity against HIV1 isolate R8 harboring reverse transcriptase Y181C and K103N mutant relative to drug-sensitive HIV1 CNDO
|
Human immunodeficiency virus 1
|
organism-based format
|
Scientific Literature
| ||||
10. |
F
|
Inhibition of long-lasting type calcium current (hICa) in Chinese Hamster Ovary (CHO) cells expressing hCav1.2 measured using IonWorks Quattro automated patch clamp platform
|
Cricetulus griseus
|
cell-based format
|
Scientific Literature
| ||||
11. |
A
|
fCmax in human plasma at 200 mg bid after 8 days
|
Homo sapiens
|
organism-based format
|
Scientific Literature
| ||||
12. |
P
|
Lipophilicity, log P of the compound
|
---
|
small-molecule physicochemical format
|
Scientific Literature
| ||||
13. |
B
|
Inhibition of wild-type HIV-1 3B reverse transcriptase infected in human MT4 cells assessed as reduction in virus-induced cytopathic effect after 5 days by MTT assay
|
Human immunodeficiency virus 1
|
cell-based format
|
Scientific Literature
| ||||
14. |
B
|
Inhibition of BCRP expressed in MDCK2 cells assessed as cell growth inhibition by calcein and pheophorbide A efflux assays
|
---
|
cell-based format
|
Scientific Literature
| ||||
15. |
A
|
Cmax in healthy human plasma at 200 mg, po twice a day for 8 days by reverse-phase HPLC-MS method
|
Homo sapiens
|
organism-based format
|
Scientific Literature
| ||||
16. |
T
|
Sub-acute toxicity in Kunming mouse assessed as alveolar hemorrhage at 50 mg/kg/day, po administered for 2 weeks by hematoxylin and eosin staining-based assay
|
Mus musculus
|
organism-based format
|
Scientific Literature
| ||||
17. |
P
|
Aqueous solubility of the compound in pH 7 buffer
|
---
|
small-molecule physicochemical format
|
Scientific Literature
| ||||
18. |
A
|
Induction of CYP3A4 in human assessed as reduction in sildenafil AUC
|
Homo sapiens
|
single protein format
|
Scientific Literature
| ||||
19. |
F
|
Antiviral activity against HIV1 isolate R8 harboring reverse transcriptase Y181I mutant relative to drug-sensitive HIV1 CNDO
|
Human immunodeficiency virus 1
|
organism-based format
|
Scientific Literature
| ||||
20. |
B
|
Inhibition of MRP1 expressed in MDCK2 cells assessed as cell growth inhibition by calcein and pheophorbide A efflux assays
|
---
|
cell-based format
|
Scientific Literature
|
Showing 1-20
out of 1,527 records

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