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Name | CHEMBL565799 |
---|---|
Molecular formula | C27H19Cl2FN2O3S2 |
IUPAC name | (E)-N-(4,5-dichlorothiophen-2-yl)sulfonyl-3-[5-fluoro-3-methyl-1-(naphthalen-2-ylmethyl)indol-7-yl]prop-2-enamide |
Molecular weight | 573.478 |
Hydrogen bond acceptor | 5 |
Hydrogen bond donor | 1 |
XlogP | 7.7 |
Synonyms | 4,5-Dichlorothiophene-2-sulfonic Acid[(E)-3-(5-Fluoro-3-methyl-1-naphthalen-2-ylmethyl-1H-indol-7-yl)acryloyl]amide BDBM50303661 |
Inchi Key | HIZNWXUSWJBZEM-CMDGGOBGSA-N |
Inchi ID | InChI=1S/C27H19Cl2FN2O3S2/c1-16-14-32(15-17-6-7-18-4-2-3-5-19(18)10-17)26-20(11-21(30)12-22(16)26)8-9-24(33)31-37(34,35)25-13-23(28)27(29)36-25/h2-14H,15H2,1H3,(H,31,33)/b9-8+ |
PubChem CID | 44627515 |
ChEMBL | CHEMBL565799 |
IUPHAR | N/A |
BindingDB | 50303661 |
DrugBank | N/A |
Structure | |
Lipinski's druglikeness | This ligand is heavier than 500 daltons. This ligand has a partition coefficient log P greater than 5. |
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GLASS ID | Name | UniProt | Gene | Species | Length |
---|---|---|---|---|---|
116184 | Prostacyclin receptor | P43119 | PTGIR | Homo sapiens (Human) | 386 |
116187 | Prostaglandin E2 receptor EP1 subtype | P34995 | PTGER1 | Homo sapiens (Human) | 402 |
116186 | Prostaglandin E2 receptor EP2 subtype | P43116 | PTGER2 | Homo sapiens (Human) | 358 |
116183 | Prostaglandin E2 receptor EP3 subtype | P43115 | PTGER3 | Homo sapiens (Human) | 390 |
116188 | Prostaglandin E2 receptor EP3 subtype | P30557 | Ptger3 | Mus musculus (Mouse) | 365 |
116185 | Prostaglandin E2 receptor EP4 subtype | P35408 | PTGER4 | Homo sapiens (Human) | 488 |
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