Piperacillin

Piperacillin

SCHEMBL33894

CCN1CCN(C(=O)N[C@@H](C(=O)N[C@@H]2C(=O)N3[C@@H]2SC(C)(C)[C@@H]3C(=O)O)c2ccccc2)C(=O)C1=O

nearest known ligand 0.86

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Piperacillin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 2/20 0.77
▸ KMT2A Q03164 2/20 0.77
▸ CCKBR P32239 1/20 0.77
▸ LMNA P02545 3/20 0.67
▸ KDM4E B2RXH2 3/20 0.59
▸ RECQL P46063 3/20 0.59
▸ TDP1 Q9NUW8 2/20 0.59
▸ POLB P06746 1/20 0.59
▸ HPGD P15428 1/20 0.59
▸ TEK Q02763 1/20 0.59
▸ SLC15A2 Q16348 1/20 0.59
▸ TSHR P16473 1/20 0.58
▸ CA1 P00915 8/20 0.58
▸ CA2 P00918 8/20 0.58
▸ PTGS1 P23219 1/20 0.56

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
Piperacillin SCHEMBL27343970 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL10477435 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL13788683 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL13788684 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL11908507 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL24437361 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL3233001 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL4486297 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL14506140 1.00 MEN1 (0.77) MEN1KMT2ACCKBRLMNAKDM4E
Piperacillin SCHEMBL41302 0.99 MEN1 (0.76) MEN1KMT2ACCKBRLMNAKDM4E

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

Appears in 35100 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4747395-A1 A KIT FOR IDENTIFYING BACTERIA AND DETERMINING ANTIBIOTIC SENSITIVITY Diagopreutic Private Limited (IN) 2026-05-27 — — EP claimed
US-12636268-B2 CXCL8 inhibitors for use in the treatment of COVID-19 DOMPE' FARMACEUTICI SPA (IT) 2026-05-26 — — US claimed
US-12637481-B2 Boronic acid derivatives and therapeutic uses thereof QPEX BIOPHARMA, INC. (US) 2026-05-26 — — US claimed
WO-2026104587-A1 CYCLIC BORONIC ACID ESTERS USEFUL AS ADJUVANTS IN THE TREATMENT OF BACTERIAL INFECTIONS ADJUTEC PHARMA AS (NO) 2026-05-21 — — WO claimed
EP-4041275-B1 TREATMENT AND PREVENTION OF NEPHROTOXIN-INDUCED KIDNEY INJURIES FARSIGHT MEDICAL TECH SHANGHAI CO LTD (CN) 2026-05-20 — — EP claimed
EP-4743153-A1 MEDICAL SYSTEMS FOR TREATING CONDITIONS AND DISEASES OF THE PATIENT'S BODY CAVITIES UTT Urine Topical Treatment Ltd (IL) 2026-05-20 — — EP claimed
CN-122036889-A Cyclized antibacterial peptide CycP-1 of targeted multi-drug resistant klebsiella pneumoniae, composition and application thereof 湖北江夏实验室 2026-05-15 — — CN claimed
CN-122031784-A Preparation method of microporous polylactic acid drug-loaded coating 浙江药科职业大学 2026-05-15 — — CN claimed
EP-4739326-A2 PRODUCTION & SECRETION OF AUXIN-LIKE MOLECULES IN BACTERIA SNIPR Biome ApS (DK) 2026-05-13 — — EP claimed
EP-4255391-B1 LUMINOL FOR USE IN THE TREATMENT OF SEQUELAE OF A SARS-COV-2 INFECTION METRIOPHARM AG (CH) 2026-05-06 — — EP claimed
EP-0138523-A1 Penicillin derivatives and process for preparing the same (11111) TAIHO PHARMACEUTICAL COMPANY LIMITED (JP) 1985-04-24 — — EP claimed
US-4503040-A 6-(Aminoacyloxymethyl)penicillanic acid 1,1-dioxides as beta-lactamase inhibitors PFIZER INC. (US) 1985-03-05 — — US claimed
US-4452796-A ANTIBIOTICS PFIZER INC. (US) 1984-06-05 — — US claimed
EP-0108295-A1 Oral dosage form F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-05-16 — — EP claimed
US-4427678-A 6-Aminomethylpenicillanic acid 1,1-dioxide derivatives as beta-lactamase inhibitors PFIZER INC. (US) 1984-01-24 — — US claimed
EP-0084925-A1 6-Aminoalkylpenicillanic acid 1,1-dioxides and derivatives as beta-lactamase inhibitors PFIZER INC. (US) 1983-08-03 — — EP claimed
EP-0050965-A1 Beta-lactamase inhibitory composition Takeda Chemical Industries, Ltd. (JP) 1982-05-05 — — EP claimed
EP-0004925-B1 SYNERGISTIC MIXTURES OF ANTIBIOTICS AND PROCESS FOR THEIR PRODUCTION CIBA-GEIGY AG (CH) 1982-02-24 — — EP claimed
EP-0026409-A1 Combinations of active ingredients, pharmaceutical preparations, as well as their preparation F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1981-04-08 — — EP claimed
EP-0004925-A1 Synergistic mixtures of antibiotics and process for their production CIBA-GEIGY AG (CH) 1979-10-31 — — EP claimed
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