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TargetBeta-2-microglobulin
LigandBDBM55038
Substrate/Competitorn/a
Meas. Tech.Fluorescence Assay
pH7.4±0
Temperature310.15±0 K
IC50 6.9e+4± 9e+3 nM
Citation Giorgetti, SRaimondi, SPagano, KRelini, ABucciantini, MCorazza, AFogolari, FCodutti, LSalmona, MMangione, PColombo, LDe Luigi, APorcari, RGliozzi, AStefani, MEsposito, GBellotti, VStoppini, M Effect of tetracyclines on the dynamics of formation and destructuration of beta2-microglobulin amyloid fibrils. J Biol Chem286:2121-31 (2011) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Beta-2-microglobulin
Name:Beta-2-microglobulin
Synonyms:B2M | B2MG_HUMAN
Type:Enzyme
Mol. Mass.:13714.40
Organism:Homo sapiens (Human)
Description:P61769
Residue:119
Sequence:
MSRSVALAVLALLSLSGLEAIQRTPKIQVYSRHPAENGKSNFLNCYVSGFHPSDIEVDLL
KNGERIEKVEHSDLSFSKDWSFYLLYYTEFTPTEKDEYACRVNHVTLSQPKIVKWDRDM
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BDBM55038
n/a
NameBDBM55038
Synonyms:(2E,4S,4aR,5S,5aR,12aS)-2-[amino(hydroxy)methylene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methylene-4,4a,5,5a-tetrahydrotetracene-1,3,12-trione;hydrochloride | (2E,4S,4aR,5S,5aR,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methylene-4,4a,5,5a-tetrahydrotetracene-1,3,12-trione;hydrochloride | (2E,4S,4aR,5S,5aR,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methylidene-4,4a,5,5a-tetrahydrotetracene-1,3,12-trione;hydrochloride | (2E,4S,4aR,5S,5aR,12aS)-2-[azanyl(oxidanyl)methylidene]-4-(dimethylamino)-6-methylidene-5,10,11,12a-tetrakis(oxidanyl)-4,4a,5,5a-tetrahydrotetracene-1,3,12-trione;hydrochloride | (4S,4aR,5S,5aR,12aR)-4-(dimethylamino)-1,5,10,11,12a-pentahydroxy-3,12-diketo-6-methylene-4,4a,5,5a-tetrahydrotetracene-2-carboxamide;hydrochloride | (4S,4aR,5S,5aS,12aS)-4-(dimethylamino)-5,10,12a-trihydroxy-1,3,11,12-tetraketo-6-methylene-4a,5,5a,11a-tetrahydro-4H-tetracene-2-carboxamide;hydrochloride | MLS001049011 | Methacycline | SMR000387056 | cid_16196941
TypeSmall organic molecule
Emp. Form.C22H22N2O8
Mol. Mass.442.4187
SMILESCN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(C(=O)c4c(O)cccc4C3=C)C(=O)[C@]2(O)C(=O)C(C(N)=O)C1=O
Structure
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