Compound Detail
CHEMBL1784269
ARCHAZOLID F Enter ChEMBL ID:
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CNC(=O)O[C@@H](CC(C)C)c1nc([C@H]2OC(=O)C/C=C/C(C)=C/[C@@H](O)[C@@H](C)/C=C(C)\C=C(C)/C=C/[C@@H](O)[C@H](C)[C@H](OC)/C(C)=C/C=C/[C@@H]2C)cs1
Basic Information
| ChEMBL ID | CHEMBL1784269 |
| Name | ARCHAZOLID F |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | WRJITTKUXGEQBF-KJKBHKFMSA-N |
4
Targets
5
Activities
2
Assay Types
1
PK Parameters
17
Publications
0
Known Names
Molecular Properties
725.0
MW (Da)
8.67
ALogP
9
HBA
3
HBD
127.2
PSA (Ų)
0.25
QED
2
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 4 meas. best 8.35
Ki 1 meas. best 6.07
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Unchecked CHEMBL612545 | IC50 | 8.35 | 8.275 | 4.5 | 2 |
| P2X purinoceptor 3 CHEMBL2998 | IC50 | 6.36 | 6.36 | 438.0 | 1 |
| Neutrophil elastase CHEMBL248 | IC50 | 6.08 | 6.08 | 830.0 | 1 |
| Adenosine receptor A3 CHEMBL256 | Ki | 6.07 | 6.07 | 859.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 271.0 | mL.min-1.g-1 | Mus musculus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Unchecked | IC50 | = | 4.51 | nM | 8.35 | Growth inhibition of human 1321N1 cells incubated for 72 hrs by MTT assay | 31990540 |
| Unchecked | IC50 | = | 6.26 | nM | 8.2 | Inhibition of Manduca sexta V-type proton ATPase assessed as reduction in inorga... | 31990540 |
| P2X purinoceptor 3 | IC50 | = | 438.0 | nM | 6.36 | Inhibition of human P2X3 assessed as reduction in agonist-induced intracellular ... | 31990540 |
| Neutrophil elastase | IC50 | = | 830.0 | nM | 6.08 | Inhibition of human leukocyte elastase assessed as reduction in pNA release usin... | 31990540 |
| Adenosine receptor A3 | Ki | = | 859.0 | nM | 6.07 | Displacement of [3H]PSB-11 from human A3 adenosine receptor expressed in CHO cel... | 31990540 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 31990540 | 10.1021/acs.jmedchem.9b01887 | ADMET | 7 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Unchecked | 2 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Neutrophil elastase | 1 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Chymotrypsin | 1 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Procathepsin L | 1 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Cathepsin B | 1 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Trypsin | 1 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | P2X purinoceptor 3 | 1 |
| 31990540 | 10.1021/acs.jmedchem.9b01887 | Adenosine receptor A3 | 1 |
| 21513292 | 10.1021/np200036v | L929 | 1 |
| 21513292 | 10.1021/np200036v | MCF7 | 1 |
| 21513292 | 10.1021/np200036v | PC-3 | 1 |
| 21513292 | 10.1021/np200036v | A-431 | 1 |
| 21513292 | 10.1021/np200036v | SK-OV-3 | 1 |
| 21513292 | 10.1021/np200036v | U-937 | 1 |
| 21513292 | 10.1021/np200036v | NON-PROTEIN TARGET | 1 |
| 21513292 | 10.1021/np200036v | V-type proton ATPase subunit B | 1 |
Data from ChEMBL 36 via Core Engine