Carbenicillin Phenyl

Carbenicillin Phenyl

SCHEMBL10734854

CC1(C)S[C@@H]2C(NC(=O)C(C(=O)Oc3ccccc3)c3ccccc3)C(=O)N2[C@H]1C(=O)O

nearest known ligand 0.68

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 7/20 0.68
▸ RECQL P46063 4/20 0.68
▸ TDP1 Q9NUW8 3/20 0.68
▸ KMT2A Q03164 3/20 0.68
▸ POLB P06746 2/20 0.68
▸ MEN1 O00255 2/20 0.68
▸ HPGD P15428 1/20 0.68
▸ TEK Q02763 1/20 0.68
▸ SLC15A2 Q16348 1/20 0.68
▸ LMNA P02545 5/20 0.67
▸ TSHR P16473 1/20 0.67
▸ PTGS1 P23219 2/20 0.65
▸ RARB P10826 1/20 0.58
▸ RARG P13631 1/20 0.58
▸ NR1H2 P55055 1/20 0.58
▸ NR1H3 Q13133 1/20 0.58
▸ NR1I3 Q14994 1/20 0.58
▸ CYP3A4 P08684 2/20 0.58
▸ HSD17B10 Q99714 2/20 0.58
▸ GLA P06280 1/20 0.57

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.

Compoundsimilaritytop predictedshared targets
Carbenicillin Phenyl SCHEMBL150615 1.00 KDM4E (0.68) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL150616 1.00 KDM4E (0.68) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL11310099 1.00 KDM4E (0.68) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL586468 0.99 KDM4E (0.67) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL11308037 0.99 KDM4E (0.67) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL11475569 0.99 KDM4E (0.67) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL11310839 0.94 LMNA (0.64) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL11310852 0.94 LMNA (0.64) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL192220 0.92 LMNA (0.79) KDM4ERECQLTDP1KMT2APOLB
Carbenicillin Phenyl SCHEMBL11308035 0.92 LMNA (0.79) KDM4ERECQLTDP1KMT2APOLB

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0083977-A1 6-Alpha-hydroxymethylpenicillanic acid sulfone as a beta-lactamase inhibitor PFIZER INC. (US) 1983-07-20 — — 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
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
US-4656263-A 6-β-substituted penicillanic acid compound free of the 6-α-epimer PFIZER INC. (US) 1987-04-07 — — US disclosed
EP-0095341-B1 PENICILLANIC ACID DIOXIDE PRODRUG PFIZER INC. (US) 1986-02-26 — — EP disclosed
US-4518530-A 6-β-Substituted penicillanic acids as β-lactamase inhibitors PFIZER INC. (US) 1985-05-21 — — US disclosed
US-4517126-A Penicillanic acid derivative PFIZER INC. (US) 1985-05-14 — — US disclosed
US-4432970-A SYNERGISTIC WITH AMINO ACID DERIVATIVE ANTIBIOTICS PFIZER INC. (US) 1984-02-21 — — US disclosed
US-4428935-A BETA-LACTAMASE INHIBITORS PFIZER INC. (US) 1984-01-31 — — US disclosed
EP-0095341-A1 Penicillanic acid dioxide prodrug PFIZER INC. (US) 1983-11-30 — — EP disclosed
US-4397783-A HYDRODEHALOGENATION WITH AN ORGANOTIN HYDRIDE PFIZER INC. (US) 1983-08-09 — — US disclosed
EP-0083977-A1 6-Alpha-hydroxymethylpenicillanic acid sulfone as a beta-lactamase inhibitor PFIZER INC. (US) 1983-07-20 — — EP disclosed
EP-0008917-B1 PENAM-3-CARBOXYLIC ACID 1,1-DIOXIDES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS PFIZER INC. (US) 1982-11-24 — — EP 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
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