⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL345526 | 0.67 | — | — | |
| SCHEMBL4584754 | 0.56 | — | — | |
| SCHEMBL13523738 | 0.56 | — | — | |
| SCHEMBL7844155 | 0.55 | — | — | |
| SCHEMBL8120650 | 0.55 | CA1 (0.38) | — | |
| SCHEMBL24459 | 0.45 | — | — | |
| Methane SCHEMBL23044967 | 0.32 | — | — | |
| SCHEMBL6264766 | 0.32 | — | — | |
| SCHEMBL1170 | 0.32 | — | — | |
| SCHEMBL8425118 | 0.32 | — | — |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-112930192-A | Nipah virus immunogens and uses thereof | 美国政府(由卫生和人类服务部的部长所代表) | 2021-06-08 | — | — | CN | disclosed |
| CN-102459362-A | Catalyst component for the polymerization of olefins and catalyst obtained therefrom | BASELL POLIOLEFINE SRL | 2012-05-16 | — | — | CN | disclosed |
| EP-1182180-B1 | Process for the dehydrogenation of organic compounds in the presence of a bimetallic catalyst | INST FRANCAIS DU PETROLE (FR) | 2010-05-12 | — | — | EP | disclosed |
| CN-100473640-C | Method for preparing optical pure trans 2,3-diamine-1,2,3,4-tetrahydrogenated naphthalene | SHANGHAI YAOMING KANGDE NEW FH (CN) | 2009-04-01 | — | — | CN | disclosed |
| EP-1181978-B1 | Bimetallic supported catalyst having a strong interaction between a metal of the group VIII and tin and the use thereof in a catalytic reforming process | INST FRANCAIS DU PETROLE (FR) | 2008-02-06 | — | — | EP | disclosed |
| CN-1623976-A | Method for preparing optical pure trans 2,3-diamine-1,2,3,4-tetrahydrogenated naphthalene | YAOMING KANGDE NEW FHARMACEUTI (CN) | 2005-06-08 | — | — | CN | disclosed |
| CN-1137085-C | Process for preparation of 5,6-dihydroxyl-2-amino-1,2,3,4-tetrahydronaphthalene derivatives | ������˹ҩƷ��˾ | 2004-02-04 | — | — | CN | disclosed |
| EP-1182180-A1 | Process for the dehydrogenation of organic compounds in the presence of a bimetallic catalyst | INSTITUT FRANCAIS DU PETROLE (FR) | 2002-02-27 | — | — | EP | disclosed |
| EP-1181978-A1 | Bimetallic supported catalyst having a strong interaction between a metal of the group VIII and tin and the use thereof in a catalytic reforming process | INSTITUT FRANCAIS DU PETROLE (FR) | 2002-02-27 | — | — | EP | disclosed |
| CN-1073984-C | Process for preparing 5, 6-dihydroxy-2-amino-1, 2,3, 4-tetrahydronaphthalene derivatives | CHIESI FARMA SPA (IT) | 2001-10-31 | — | — | CN | disclosed |
| CN-1278528-A | Process for preparation of 5,6-dihydroxyl-2-amino-1,2,3,4-tetrahydronaphthalene derivatives | CHIESI PHARMACEUTICAL S P A (IT) | 2001-01-03 | — | — | CN | disclosed |
| CN-1278527-A | Process for preparation of 5,6-dihydrxyl-2-amino-1,2,3,4-tetrahydronaphthalene derivatives | CHIESI PHARMACEUTICAL S P A (IT) | 2001-01-03 | — | — | CN | disclosed |
| CN-1278526-A | Process for preparation of 5,6-dihydroxyl-2-amino-1,2,3,4-tetrahydronaphthalene derivatives | CHIESI PHARMACEUTICAL S P A (IT) | 2001-01-03 | — | — | CN | disclosed |
| CN-1147808-A | Process for preparing 5, 6-dihydroxy-2-amino-1, 2, 3, 4-tetrahydronaphthalene derivatives | CHIESI FARMA SPA (IT) | 1997-04-16 | — | — | CN | disclosed |