Known targets — ChEMBL curated mechanism
The experimentally established mechanism targets of Carbenicillin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PTGS1 | P23219 | 3/20 | 0.77 |
| ▸ | KDM4E | B2RXH2 | 9/20 | 0.77 |
| ▸ | RECQL | P46063 | 4/20 | 0.77 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.77 |
| ▸ | HPGD | P15428 | 3/20 | 0.77 |
| ▸ | POLB | P06746 | 2/20 | 0.77 |
| ▸ | MEN1 | O00255 | 2/20 | 0.77 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.77 |
| ▸ | TEK | Q02763 | 1/20 | 0.77 |
| ▸ | SLC15A2 | Q16348 | 1/20 | 0.77 |
| ▸ | LMNA | P02545 | 4/20 | 0.75 |
| ▸ | TSHR | P16473 | 1/20 | 0.75 |
| ▸ | RARB | P10826 | 1/20 | 0.64 |
| ▸ | RARG | P13631 | 1/20 | 0.64 |
| ▸ | NR1H2 | P55055 | 1/20 | 0.64 |
| ▸ | NR1H3 | Q13133 | 1/20 | 0.64 |
| ▸ | NR1I3 | Q14994 | 1/20 | 0.64 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.63 |
| ▸ | GLA | P06280 | 1/20 | 0.63 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.63 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| Carbenicillin SCHEMBL11310979 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL3375 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL11310973 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL13662704 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL320405 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL11604897 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL8402462 | 1.00 | PTGS1 (0.77) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL193749 | 0.99 | PTGS1 (0.76) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL28801787 | 0.99 | PTGS1 (0.76) | PTGS1KDM4ERECQLTDP1HPGD | |
| Carbenicillin SCHEMBL7341688 | 0.99 | PTGS1 (0.76) | PTGS1KDM4ERECQLTDP1HPGD |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0074783-B1 | BETA-LACTAMASE INHIBITING 2-BETA-SUBSTITUTED-2-ALPHA-METHYL-(5R) PENAM-3-ALPHA-CARBOXYLIC ACID 1,1-DIOXIDES AND INTERMEDIATES THEREFOR | PFIZER INC. (US) | 1985-07-31 | — | — | EP | claimed |
| US-4432970-A | SYNERGISTIC WITH AMINO ACID DERIVATIVE ANTIBIOTICS | PFIZER INC. (US) | 1984-02-21 | — | — | US | claimed |
| EP-0083977-A1 | 6-Alpha-hydroxymethylpenicillanic acid sulfone as a beta-lactamase inhibitor | PFIZER INC. (US) | 1983-07-20 | — | — | EP | claimed |
| EP-0074783-A1 | Beta-lactamase inhibiting 2-beta-substituted-2-alpha-methyl-(5R) penam-3-alpha-carboxylic acid 1,1-dioxides and intermediates therefor | PFIZER INC. (US) | 1983-03-23 | — | — | EP | claimed |
| EP-0008917-B1 | PENAM-3-CARBOXYLIC ACID 1,1-DIOXIDES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS | PFIZER INC. (US) | 1982-11-24 | — | — | EP | claimed |
| US-4287181-A | TO ENHANCE THE EFFECTIVENESS OF B-LACTAM ANTIBIOTICS | PFIZER INC. (US) | 1981-09-01 | — | — | US | claimed |
| US-4256733-A | Acetoxymethyl penam compounds as β-lactamase inhibitors | PFIZER INC. (US) | 1981-03-17 | — | — | US | claimed |
| US-4234579-A | Penicillanic acid 1,1-dioxides as β-lactamase inhibitors | PFIZER INC. (US) | 1980-11-18 | — | — | US | claimed |
| EP-0008917-A1 | Penam-3-carboxylic acid 1,1-dioxides, process for their preparation and pharmaceutical compositions | PFIZER INC. (US) | 1980-03-19 | — | — | EP | claimed |
| EP-0181702-B1 | 6-SUBSTITUTED PENICILLANIC ACID 1,1-DIOXIDE COMPOUNDS | PFIZER INC. (US) | 1989-05-31 | — | — | EP | disclosed |
| US-4762920-A | BETA-LACTAMASE INHIBITOR, SYNERGISTIC WITH PENICILLIN ANTIBIOTICS AND BACTERICIDES | PFIZER, INC. (US) | 1988-08-09 | — | — | US | disclosed |
| US-4714761-A | OXIDATION, DEHALOGENATION | PFIZER INC. (US) | 1987-12-22 | — | — | US | disclosed |
| US-4656263-A | 6-β-substituted penicillanic acid compound free of the 6-α-epimer | PFIZER INC. (US) | 1987-04-07 | — | — | US | disclosed |
| US-4613462-A | ANTIBIOTICS | PFIZER, INC. (US) | 1986-09-23 | — | — | US | disclosed |
| US-4287181-A | TO ENHANCE THE EFFECTIVENESS OF B-LACTAM ANTIBIOTICS | PFIZER INC. (US) | 1981-09-01 | — | — | US | disclosed |
| US-4256733-A | Acetoxymethyl penam compounds as β-lactamase inhibitors | PFIZER INC. (US) | 1981-03-17 | — | — | US | disclosed |
| US-4241050-A | Penam 1,1-dioxides as beta-lactamase inhibitors | PFIZER INC. (US) | 1980-12-23 | — | — | US | disclosed |
| US-4234579-A | Penicillanic acid 1,1-dioxides as β-lactamase inhibitors | PFIZER INC. (US) | 1980-11-18 | — | — | US | disclosed |
| EP-0008917-A1 | Penam-3-carboxylic acid 1,1-dioxides, process for their preparation and pharmaceutical compositions | PFIZER INC. (US) | 1980-03-19 | — | — | EP | disclosed |
| US-4066664-A | Intermediates for preparing α-carboxy-α-(3-thienyl)penicillin and cephalosporin derivatives | RECHERCHE ET INDUSTRIE THERAPEUTIQUES (BE) | 1978-01-03 | — | — | US | disclosed |