Cefprozil

Cefprozil

SCHEMBL37024

CC=CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)c3ccc(O)cc3)[C@H]2SC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Cefprozil. 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
▸ PTGS2 P35354 2/20 1.00
▸ DRD2 P14416 1/20 1.00
▸ DRD3 P35462 1/20 1.00
▸ MAPT P10636 8/20 0.98
▸ ALDH1A1 P00352 7/20 0.98
▸ KMT2A Q03164 6/20 0.98
▸ MEN1 O00255 5/20 0.98
▸ HSD17B10 Q99714 7/20 0.75
▸ SLC15A2 Q16348 3/20 0.75
▸ LMNA P02545 2/20 0.75
▸ ESR1 P03372 1/20 0.75
▸ SLC22A6 Q4U2R8 1/20 0.75
▸ SLC22A8 Q8TCC7 1/20 0.75
▸ CYP3A4 P08684 4/20 0.63
▸ HPGD P15428 3/20 0.63
▸ TDP1 Q9NUW8 3/20 0.63
▸ BLM P54132 2/20 0.63
▸ CYP2C19 P33261 2/20 0.63
▸ MAPK1 P28482 1/20 0.63
▸ ADRA1A P35348 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
Cefprozil Anhydrous, (E)- SCHEMBL16072814 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL9177544 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL18814837 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL14108301 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL5191958 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL10801275 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL7586258 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL2901170 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL14064854 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1
Cefprozil Anhydrous, (E)- SCHEMBL37023 1.00 PTGS2 (1.00) PTGS2DRD2DRD3MAPTALDH1A1

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 24310 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12637481-B2 Boronic acid derivatives and therapeutic uses thereof QPEX BIOPHARMA, INC. (US) 2026-05-26 — — US claimed
CN-115215923-B Macrocyclic broad-spectrum antibiotics 豪夫迈·罗氏有限公司 2026-05-19 — — CN claimed
EP-4740962-A1 PHARMACEUTICAL COMPOSITION, FORMULATION CONTAINING PHARMACEUTICAL COMPOSITION, KIT CONTAINING PHARMACEUTICAL COMPOSITION, PREPARATION METHOD FOR PHARMACEUTICAL COMPOSITION, AND USE OF PHARMACEUTICAL COMPOSITION Shanghai WD Pharmaceutical Co., Ltd (CN) 2026-05-13 — — EP claimed
EP-4739326-A2 PRODUCTION & SECRETION OF AUXIN-LIKE MOLECULES IN BACTERIA SNIPR Biome ApS (DK) 2026-05-13 — — EP claimed
US-20260115234-A1 PRODUCTION & SECRETION OF AUXIN-LIKE MOLECULES IN BACTERIA SNIPR BIOME APS (DK) 2026-04-30 — — US claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 — — US claimed
EP-4724049-A1 MODIFIED RELEASE FILL COMPOSITIONS FOR DOSAGE FORMS AND METHODS OF PREPARATION AND USE THEREOF Catalent Ontario Limited (CA) 2026-04-15 — — EP claimed
US-20260091089-A1 Pyocyanine Demethylases and related Phenazine Degrading Agents Compositions, Methods and Systems for Interfering with Viability of Bacteria CALIFORNIA INST OF TECHN (US) 2026-04-02 — — US claimed
US-12590108-B2 Boracic acid compound PHAENO THERAPEUTICS CO., LTD (CN) 2026-03-31 — — US claimed
US-12576124-B2 Formulation of a conjugate of a tubulysin analog to a cell-binding molecule HANGZHOU DAC BIOTECH CO., LTD (CN) 2026-03-17 — — US claimed
WO-1998022091-A1 PHARMACEUTICAL PREPARATIONS FOR THE CONTROLLED RELEASE OF β-LACTAM ANTIBIOTICS YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM (IL) 1998-05-28 — — WO claimed
WO-1998018610-A1 EMBEDDING AND ENCAPSULATION OF CONTROLLED RELEASE PARTICLES LENGERICH BERNHARD H VAN (US) 1998-05-07 — — WO claimed
WO-1998007745-A9 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING ANALOGUES OF INDOLICIDIN — 1998-04-23 — — WO claimed
WO-1998007745-A2 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING ANALOGUES OF INDOLICIDIN MICROLOGIX BIOTECH, INC. (CA) 1998-02-26 — — WO claimed
WO-1998004732-A1 SYNTHESIS OF β-LACTAM ANTIBACTERIALS USING SOLUBLE SIDE CHAIN ESTERS AND ENZYME ACYLASE BRISTOL-MYERS SQUIBB COMPANY (US) 1998-02-05 — — WO claimed
WO-1997029765-A1 ANTIMICROBIAL PEPTIDES AND METHODS OF USE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1997-08-21 — — WO claimed
EP-0680322-A1 PHARMACEUTICAL FORMULATIONS COMPRISING CLAVULANIC ACID ALONE OR IN COMBINATION WITH OTHER BETA-LACTAM ANTIBIOTICS SMITHKLINE BEECHAM PLC (GB) 1995-11-08 — — EP claimed
EP-0678095-A1 CRYSTALLINE PENICILLIN DERIVATIVE, AND ITS PRODUCTION AND USE TAIHO PHARMACEUTICAL CO., LTD. (JP) 1995-10-25 — — EP claimed
WO-1995012601-A1 CRYSTALLINE PENICILLIN DERIVATIVE, AND ITS PRODUCTION AND USE TAIHO PHARMACEUTICAL CO., LTD. (JP) 1995-05-11 — — WO claimed
WO-1994016696-A1 PHARMACEUTICAL FORMULATIONS COMPRISING CLAVULANIC ACID ALONE OR IN COMBINATION WITH OTHER BETA-LACTAM ANTIBIOTICS SMITHKLINE BEECHAM PLC (GB) 1994-08-04 — — WO claimed
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