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TargetPannexin-1
LigandBDBM50247012
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2122674 (CHEMBL4831907)
IC50 10000±n/a nM
Citation Crocetti, LGuerrini, GPuglioli, SGiovannoni, MPDi Cesare Mannelli, LLucarini, EGhelardini, CWang, JDahl, G Design and synthesis of the first indole-based blockers of Panx-1 channel. Eur J Med Chem223:0 (2021) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Pannexin-1
Name:Pannexin-1
Synonyms:PANX1_MOUSE | Pannexin-1 | Panx1
Type:PROTEIN
Mol. Mass.:48168.73
Organism:Mus musculus
Description:ChEMBL_120484
Residue:426
Sequence:
MAIAHLATEYVFSDFLLKEPTEPKFKGLRLELAVDKMVTCIAVGLPLLLISLAFAQEISI
GTQISCFSPSSFSWRQAAFVDSYCWAAVQQKSSLQSESGNLPLWLHKFFPYILLLFAILL
YLPALFWRFSAAPHLCSDLKFIMEELDKVYNRAIKAAKSARDLDLRDGPGPPGVTENVGQ
SLWEISESHFKYPIVEQYLKTKKNSSHLIMKYISCRLVTFVVILLACIYLSYYFSLSSLS
DEFLCSIKSGVLKNDSTIPDRFQCKLIAVGIFQLLSLINLIVYALLIPVVVYTFFIPFRQ
KTDILKVYEILPTFDVLHFKSEGYNDLSLYNLFLEENISELKSYKCLKVLENIKSNGQGI
DPMLLLTNLGMIKMDIIDGKIPTSLQTKGEDQGSQRVEFKDLDLSSEAAANNGEKNSRQR
LLNPSC
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  Blast E-value cutoff:
BDBM50247012
n/a
NameBDBM50247012
Synonyms:3beta-O-Succinyl-18-beta-glycyrrhetinic acid | Carbenoxolone | US11660306, Example Carbeanoxolone
TypeSmall organic molecule
Emp. Form.C34H50O7
Mol. Mass.570.7566
SMILESCC1(C)[C@H](CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O)OC(=O)CCC(O)=O |r,t:18|
Structure
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