Reaction Details |
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Target | Histidine-rich protein PFHRP-II |
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Ligand | BDBM50202611 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_423821 (CHEMBL910656) |
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IC50 | 990±n/a nM |
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Citation | Solomon, VR; Haq, W; Srivastava, K; Puri, SK; Katti, SB Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives. J Med Chem50:394-8 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histidine-rich protein PFHRP-II |
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Name: | Histidine-rich protein PFHRP-II |
Synonyms: | HRP1_PLAFA | Histidine-rich protein | Histidine-rich protein PFHRP-II |
Type: | PROTEIN |
Mol. Mass.: | 35156.49 |
Organism: | Plasmodium falciparum |
Description: | ChEMBL_500704 |
Residue: | 332 |
Sequence: | MVSFSKNKVLSAAVFASVLLLDNNNSAFNNNLCSKNAKGLNLNKRLLHETQAHVDDAHHA
HHVADAHHAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHA
ADAHHAHHAADAHHAHHAADAHHAHHAADAHHAHHAAYAHHAHHASDAHHAADAHHAAYA
HHAHHAADAHHAADAHHAAYAHHAHHAADAHHAADAHHATDAHHAHHAADAHHATDAHHA
ADAHHAADAHHATDAHHAADAHHATDAHHAADAHHAADAHHATDSHHAHHAADAHHAAAH
HATDAHHAAAHHATDAHHAAAHHEAATHCLRH
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BDBM50202611 |
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n/a |
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Name | BDBM50202611 |
Synonyms: | 3-[2-(7-chloroquinolin-4-ylamino)-ethyl]-[1,3]thiazinan-4-one | CHEMBL385783 |
Type | Small organic molecule |
Emp. Form. | C15H16ClN3OS |
Mol. Mass. | 321.825 |
SMILES | Clc1ccc2c(NCCN3CSCCC3=O)ccnc2c1 |
Structure |
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