atrasentan
chemical compound
Press Enter · cited answer in seconds
0 sources
atrasentan
Summary
atrasentan is a type of chemical entity[1]. atrasentan ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]
Key Facts
- atrasentan's instance of is recorded as type of chemical entity[3].
- atrasentan's chemical structure is recorded as Atrasentan.svg[4].
- atrasentan's physically interacts with is recorded as Endothelin receptor type A[5].
- atrasentan's physically interacts with is recorded as Endothelin receptor type B[6].
- atrasentan's CAS Registry Number is recorded as 173937-91-2[7].
- atrasentan's EC number is recorded as 681-642-4[8].
- atrasentan's canonical SMILES is recorded as CCCCN(CCCC)C(=O)CN1CC(C(C1C2=CC=C(C=C2)OC)C(=O)O)C3=CC4=C(C=C3)OCO4[9].
- atrasentan's InChI is recorded as InChI=1S/C29H38N2O6/c1-4-6-14-30(15-7-5-2)26(32)18-31-17-23(21-10-13-24-25(16-21)37-19-36-24)27(29(33)34)28(31)20-8-11-22(35-3)12-9-20/h8-13,16,23,27-28H,4-7,14-15,17-19H2,1-3H3,(H,33,34)/t23-,27-,28+/m1/s1[10].
- atrasentan's InChIKey is recorded as MOTJMGVDPWRKOC-QPVYNBJUSA-N[11].
- atrasentan's chemical formula is recorded as C₂₉H₃₈N₂O₆[12].
- atrasentan's subclass of is recorded as carboxylic acid[13].
- atrasentan's Commons category is recorded as Atrasentan[14].
- atrasentan's MeSH descriptor ID is recorded as D000077868[15].
- atrasentan's ChEMBL ID is recorded as CHEMBL9194[16].
- atrasentan's Guide to Pharmacology Ligand ID is recorded as 3487[17].
- atrasentan's Freebase ID is recorded as /m/03d2vrl[18].
- atrasentan's UNII is recorded as V6D7VK2215[19].
- atrasentan's ChemSpider ID is recorded as 140321[20].
- atrasentan's PubChem CID is recorded as 159594[21].
- atrasentan's MeSH tree code is recorded as D03.383.246.118.300[22].
- atrasentan's MeSH tree code is recorded as D03.383.773.079[23].
- atrasentan's MeSH tree code is recorded as D03.633.100.115.300[24].
- atrasentan's ChEBI ID is recorded as 135810[25].
- atrasentan's DrugBank ID is recorded as DB06199[26].
- atrasentan's isomeric SMILES is recorded as CCCCN(CCCC)C(=O)CN1CC@@HC3=CC4=C(C=C3)OCO4C@@HC3=CC4=C(C=C3)OCO4">[27].
Why It Matters
atrasentan ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2] atrasentan is known by 4 alternative names across languages and contexts.[28]