Reaction Details |
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Target | Acetolactate synthase, chloroplastic |
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Ligand | BDBM50487171 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_908731 (CHEMBL3066158) |
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Ki | 1290±n/a nM |
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Citation | Chen, CN; Chen, Q; Liu, YC; Zhu, XL; Niu, CW; Xi, Z; Yang, GF Syntheses and herbicidal activity of new triazolopyrimidine-2-sulfonamides as acetohydroxyacid synthase inhibitor. Bioorg Med Chem18:4897-904 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Acetolactate synthase, chloroplastic |
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Name: | Acetolactate synthase, chloroplastic |
Synonyms: | AHAS | ALS | Acetolactate synthase | CSR1 | ILVB_ARATH | TZP5 |
Type: | PROTEIN |
Mol. Mass.: | 72585.19 |
Organism: | Arabidopsis thaliana |
Description: | ChEMBL_934103 |
Residue: | 670 |
Sequence: | MAAATTTTTTSSSISFSTKPSPSSSKSPLPISRFSLPFSLNPNKSSSSSRRRGIKSSSPS
SISAVLNTTTNVTTTPSPTKPTKPETFISRFAPDQPRKGADILVEALERQGVETVFAYPG
GASMEIHQALTRSSSIRNVLPRHEQGGVFAAEGYARSSGKPGICIATSGPGATNLVSGLA
DALLDSVPLVAITGQVPRRMIGTDAFQETPIVEVTRSITKHNYLVMDVEDIPRIIEEAFF
LATSGRPGPVLVDVPKDIQQQLAIPNWEQAMRLPGYMSRMPKPPEDSHLEQIVRLISESK
KPVLYVGGGCLNSSDELGRFVELTGIPVASTLMGLGSYPCDDELSLHMLGMHGTVYANYA
VEHSDLLLAFGVRFDDRVTGKLEAFASRAKIVHIDIDSAEIGKNKTPHVSVCGDVKLALQ
GMNKVLENRAEELKLDFGVWRNELNVQKQKFPLSFKTFGEAIPPQYAIKVLDELTDGKAI
ISTGVGQHQMWAAQFYNYKKPRQWLSSGGLGAMGFGLPAAIGASVANPDAIVVDIDGDGS
FIMNVQELATIRVENLPVKVLLLNNQHLGMVMQWEDRFYKANRAHTFLGDPAQEDEIFPN
MLLFAAACGIPAARVTKKADLREAIQTMLDTPGPYLLDVICPHQEHVLPMIPSGGTFNDV
ITEGDGRIKY
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BDBM50487171 |
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n/a |
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Name | BDBM50487171 |
Synonyms: | CHEMBL2251948 |
Type | Small organic molecule |
Emp. Form. | C15H13Cl2N5O4S |
Mol. Mass. | 430.266 |
SMILES | COC(=O)c1cccc(Cl)c1NS(=O)(=O)c1nc2c(Cl)c(C)nc(C)n2n1 |
Structure |
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