⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL9025827 | 1.00 | — | — | |
| SCHEMBL8439763 | 0.75 | — | — | |
| SCHEMBL1061313 | 0.71 | — | — | |
| SCHEMBL16341555 | 0.66 | — | — | |
| Hydrochloric Acid SCHEMBL6732428 | 0.56 | — | — | |
| SCHEMBL17873989 | 0.56 | — | — | |
| SCHEMBL29016 | 0.53 | — | — | |
| Hydrochloric Acid SCHEMBL8386129 | 0.47 | — | — | |
| SCHEMBL2798311 | 0.47 | — | — | |
| SCHEMBL8967414 | 0.47 | — | — |
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 |
|---|---|---|---|---|---|---|---|
| EP-0711290-A1 | METHYLGUANIDINE DERIVATIVES, METHODS FOR PREPARING SAME AND COMPOSITIONS CONTAINING SAID DERIVATIVES | SANOFI (FR) | 1996-05-15 | — | — | EP | claimed |
| WO-1995004052-A1 | METHYLGUANIDINE DERIVATIVES, METHODS FOR PREPARING SAME AND COMPOSITIONS CONTAINING SAID DERIVATIVES | SANOFI (FR) | 1995-02-09 | — | — | WO | claimed |
| EP-0711290-A1 | METHYLGUANIDINE DERIVATIVES, METHODS FOR PREPARING SAME AND COMPOSITIONS CONTAINING SAID DERIVATIVES | SANOFI (FR) | 1996-05-15 | — | — | EP | disclosed |
| WO-1995004052-A1 | METHYLGUANIDINE DERIVATIVES, METHODS FOR PREPARING SAME AND COMPOSITIONS CONTAINING SAID DERIVATIVES | SANOFI (FR) | 1995-02-09 | — | — | WO | disclosed |
| EP-0327239-B1 | 1-carbacephalosporin antibiotics | LILLY CO ELI (US) | 1994-06-22 | — | — | EP | disclosed |
| US-5221739-A | Acetylation of 3-hydroxymethyl cephalosporins | ELI LILLY AND COMPANY (US) | 1993-06-22 | — | — | US | disclosed |
| EP-0511002-A2 | C-3 phosphine oxide substituted carbacephalosporins | ELI LILLY AND COMPANY (US) | 1992-10-28 | — | — | EP | disclosed |
| EP-0485103-A2 | Process for cleavage of esters during the production of cephalosporins | ELI LILLY AND COMPANY (US) | 1992-05-13 | — | — | EP | disclosed |
| US-5095107-A | Salt formation | ELI LILLY AND COMPANY (US) | 1992-03-10 | — | — | US | disclosed |
| US-5084447-A | Antibiotics as bactericides | ELI LILLY AND COMPANY (US) | 1992-01-28 | — | — | US | disclosed |
| EP-0430556-A2 | (1-Akylsubstituted) and 1,1-dialkylsubstituted) carbacephalosporins | ELI LILLY AND COMPANY (US) | 1991-06-05 | — | — | EP | disclosed |
| US-5019571-A | 1-carbacephalosporin antibiotics | ELI LILLY AND COMPANY (US) | 1991-05-28 | — | — | US | disclosed |
| EP-0353732-A2 | Fluoro-olefins, method for their preparation and their use | CIBA-GEIGY AG (CH) | 1990-02-07 | — | — | EP | disclosed |
| EP-0327239-A1 | 1-carbacephalosporin antibiotics | ELI LILLY AND COMPANY (US) | 1989-08-09 | — | — | EP | disclosed |