Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H26N6O2S |
| Molecular Weight | 402.514 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(C=CC(=N1)C(C)C)C2=CN=C3SC(=NN23)N4CCC(O)(CN)CC4
InChI
InChIKey=JYHSRMKXBAPFST-UHFFFAOYSA-N
InChI=1S/C19H26N6O2S/c1-12(2)14-5-4-13(16(22-14)27-3)15-10-21-17-25(15)23-18(28-17)24-8-6-19(26,11-20)7-9-24/h4-5,10,12,26H,6-9,11,20H2,1-3H3
| Molecular Formula | C19H26N6O2S |
| Molecular Weight | 402.514 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 19:36:43 GMT 2025
by
admin
on
Wed Apr 02 19:36:43 GMT 2025
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| Record UNII |
4HRQ96CC7C
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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4HRQ96CC7C
Created by
admin on Wed Apr 02 19:36:43 GMT 2025 , Edited by admin on Wed Apr 02 19:36:43 GMT 2025
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2640567-43-5
Created by
admin on Wed Apr 02 19:36:43 GMT 2025 , Edited by admin on Wed Apr 02 19:36:43 GMT 2025
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156274257
Created by
admin on Wed Apr 02 19:36:43 GMT 2025 , Edited by admin on Wed Apr 02 19:36:43 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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BINDER->LIGAND |
BINDING
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SALT/SOLVATE -> PARENT |
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TARGET ORGANISM->INHIBITOR |
In vitro Plasmodium blood-stage growth inhibition assays.
EC50
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TARGET ORGANISM->INHIBITOR |
In vitro Plasmodium blood-stage growth inhibition assays.
EC50
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TRANSPORTER -> SUBSTRATE |
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OFF-TARGET->INHIBITOR |
IC50
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
Fast-killing potential of has been demonstrated. no viable parasites after 24 h (5 log reduction) which is comparable to or faster than artemisinin.
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