Carbenicillin

Carbenicillin

SCHEMBL320405

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

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

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)

geneUniProtsupporting neighboursconfidence
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.

Compoundsimilaritytop predictedshared 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 SCHEMBL10520792 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 572 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250249110-A1 ANTIMICROBIAL PEPTIDE DERIVATIVE AND USE THEREOF SICHUAN UNIVERSITY (CN) 2025-08-07 US claimed
EP-3849562-B1 COMBINATION COMPOSITIONS COMPRISING A BETA-LACTAMASE INHIBITOR VENATORX PHARMACEUTICALS INC (US) 2024-06-26 EP claimed
EP-3377473-B1 MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS RQX PHARMACEUTICALS INC (US) 2024-06-19 EP claimed
EP-3781576-B1 BORONIC ACID DERIVATIVES AND THERAPEUTIC USES THEREOF QPEX BIOPHARMA INC (US) 2024-06-12 EP claimed
EP-3374391-B1 ANTIBODY MOLECULE-DRUG CONJUGATES THAT SPECIFICALLY BINDS TO LIPOPOLYSACCHARIDE AND USES THEREOF VISTERRA INC (US) 2024-04-17 EP claimed
EP-3529359-B1 TUMOR INFILTRATING LYMPHOCYTES FOR USE IN THERAPY UNIV MINNESOTA (US) 2023-12-13 EP claimed
EP-4284941-A1 DETECTING BETA-LACTAMASE ENZYME ACTIVITY Commissariat à l'Energie Atomique et aux Energies Alternatives (FR) 2023-12-06 EP claimed
EP-2916820-B1 DELIVERY OF BIOLOGICALLY-ACTIVE AGENTS USING VOLATILE, HYDROPHOBIC SOLVENTS ROCHAL TECH LLC (US) 2023-10-11 EP claimed
EP-3265119-B1 SAFE AND EFFECTIVE BETA-LACTAMASE DOSING FOR MICROBIOME PROTECTION THERIVA BIOLOGICS INC (US) 2023-10-11 EP claimed
EP-3122757-B1 CHARGED LINKERS AND THEIR USES FOR CONJUGATION HANGZHOU DAC BIOTECH CO LTD (CN) 2023-09-06 EP claimed
EP-0059645-B1 METHOD AND KIT FOR IDENTIFICATION OF BETA-LACTAMASES NATIONAL RESEARCH DEVELOPMENT CORPORATION (GB) 1986-06-04 EP claimed
EP-0085667-B1 ENZYMATIC PROCESS FOR THE DETERMINATION OF ANTIBIOTICS CONTAINING A BETA-LACTAM NUCLEUS U C B, S.A. (BE) 1986-05-07 EP claimed
EP-0084925-B1 6-AMINOALKYLPENICILLANIC ACID 1,1-DIOXIDES AND DERIVATIVES AS BETA-LACTAMASE INHIBITORS PFIZER INC. (US) 1986-04-09 EP claimed
EP-0050805-B1 BETA-LACTAMS, INTERMEDIATES AND PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1985-07-24 EP claimed
EP-0057606-B1 SALTS OF PENICILLANIC ACID 1,1-DIOXIDE PFIZER INC. (US) 1985-05-02 EP claimed
EP-0085667-A2 Enzymatic process for the determination of antibiotics containing a beta-lactam nucleus U C B, S.A. (BE) 1983-08-10 EP claimed
EP-0007690-B1 PROCESS FOR THE PRODUCTION OF A POLYSACCHARIDE TATE & LYLE PATENT HOLDINGS LIMITED (BM) 1982-10-06 EP claimed
EP-0010846-B1 METHOD AND APPARATUS FOR DETERMINING THE MINIMUM CONCENTRATION OF ANTIBIOTIC TO INHIBIT MICROORGANISM GROWTH WARNER-LAMBERT COMPANY (US) 1982-09-15 EP claimed
EP-0007717-B1 CLAVULANIC ACID DERIVATIVES, A PROCESS FOR THEIR PREPARATION, THEIR USE, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM BEECHAM GROUP PLC (GB) 1982-08-11 EP claimed
EP-0003618-B1 ANTIBACTERIAL COMPOSITION AND USE THEREOF FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1981-01-28 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250249110-A1 ANTIMICROBIAL PEPTIDE DERIVATIVE AND USE THEREOF VIP, SLC47A1, SLC47A2 PTGS1 2492/4885KDM4E 4347/4885RECQL 2595/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.