Reaction Details |
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Target | S-adenosylhomocysteine hydrolase-like protein 1 |
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Ligand | BDBM50140075 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1547422 (CHEMBL3757541) |
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IC50 | 3.2±n/a nM |
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Citation | Liu, C; Chen, Q; Schneller, SW Enantiomeric 3-deaza-1',6'-isoneplanocin and its 3-bromo analogue: Synthesis by the Ullmann reaction and their antiviral properties. Bioorg Med Chem Lett26:928-30 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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S-adenosylhomocysteine hydrolase-like protein 1 |
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Name: | S-adenosylhomocysteine hydrolase-like protein 1 |
Synonyms: | AHCYL1 | Adenosylhomocysteinase 2 | AdoHcyase 2 | DC-expressed AHCY-like molecule | DCAL | DCAL | IP(3)Rs binding protein released with IP(3) | IRBIT | SAHH2_HUMAN | XPVKONA |
Type: | PROTEIN |
Mol. Mass.: | 58952.83 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_116703 |
Residue: | 530 |
Sequence: | MSMPDAMPLPGVGEELKQAKEIEDAEKYSFMATVTKAPKKQIQFADDMQEFTKFPTKTGR
RSLSRSISQSSTDSYSSAASYTDSSDDEVSPREKQQTNSKGSSNFCVKNIKQAEFGRREI
EIAEQDMSALISLRKRAQGEKPLAGAKIVGCTHITAQTAVLIETLCALGAQCRWSACNIY
STQNEVAAALAEAGVAVFAWKGESEDDFWWCIDRCVNMDGWQANMILDDGGDLTHWVYKK
YPNVFKKIRGIVEESVTGVHRLYQLSKAGKLCVPAMNVNDSVTKQKFDNLYCCRESILDG
LKRTTDVMFGGKQVVVCGYGEVGKGCCAALKALGAIVYITEIDPICALQACMDGFRVVKL
NEVIRQVDVVITCTGNKNVVTREHLDRMKNSCIVCNMGHSNTEIDVTSLRTPELTWERVR
SQVDHVIWPDGKRVVLLAEGRLLNLSCSTVPTFVLSITATTQALALIELYNAPEGRYKQD
VYLLPKKMDEYVASLHLPSFDAHLTELTDDQAKYLGLNKNGPFKPNYYRY
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BDBM50140075 |
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n/a |
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Name | BDBM50140075 |
Synonyms: | CHEMBL3753637 |
Type | Small organic molecule |
Emp. Form. | C12H14N4O3 |
Mol. Mass. | 262.2646 |
SMILES | Nc1nccc2n(cnc12)C1=C[C@H](CO)[C@@H](O)[C@H]1O |r,t:12| |
Structure |
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