Cefdinir

Cefdinir

SCHEMBL36995

C=CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)/C(=N\O)c3csc(N)n3)[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 Cefdinir. 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
▸ TDP1 Q9NUW8 8/20 1.00
▸ MAPT P10636 5/20 1.00
▸ ABCC4 O15439 2/20 1.00
▸ CNR1 P21554 1/20 1.00
▸ CTDSP1 Q9GZU7 1/20 1.00
▸ APEX1 P27695 3/20 0.79
▸ APAF1 O14727 2/20 0.79
▸ LMNA P02545 2/20 0.79
▸ L3MBTL1 Q9Y468 2/20 0.79
▸ TSHR P16473 1/20 0.79
▸ PLCG1 P19174 1/20 0.79
▸ ABCC2 Q92887 1/20 0.79
▸ SIRT5 Q9NXA8 1/20 0.79
▸ PSMD14 O00487 1/20 0.78
▸ MMP2 P08253 1/20 0.78
▸ HPGD P15428 1/20 0.65
▸ NR1I2 O75469 5/20 0.60
▸ HTR2C P28335 1/20 0.60
▸ PPARG P37231 2/20 0.58
▸ SLC22A6 Q4U2R8 2/20 0.58

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
Cefdinir SCHEMBL3299566 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL6820723 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL2221924 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL5919457 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL3297328 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL16072816 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL1559599 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL36996 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL4114437 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1
Cefdinir SCHEMBL4114446 1.00 TDP1 (1.00) TDP1MAPTABCC4CNR1CTDSP1

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 22134 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
EP-4743122-A1 THERAPEUTIC SEALANTS BASED UPON DRUG CONJUGATES The Johns Hopkins University (US) 2026-05-20 — — EP 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-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
EP-0890359-A1 TABLETS CONTAINING BETA-LACTAM ANTIBIOTIC AND PROCESS FOR PRODUCING THE SAME FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1999-01-13 — — EP claimed
EP-0874853-A1 PROCESS FOR PREPARATION OF CEFDINIR HANMI PHARMACEUTICAL CO.,LTD. (KR) 1998-11-04 — — EP claimed
WO-1998047895-A1 2-OXO-1-AZETIDINE SULFONIC ACID DERIVATIVES AS POTENT β-LACTAMASE INHIBITORS NAEJA PHARMACEUTICAL INC. (US) 1998-10-29 — — WO claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 — — US claimed
US-5763603-A HIGH BETA-LACTAMASE INHIBITORY ACTIVITY IN COMBINATION WITH BETA-LACTAM ANTIBIOTICS TAIHO PHARMACEUTICAL CO., LTD. (JP) 1998-06-09 — — US claimed
WO-1997024358-A1 PROCESS FOR PREPARATION OF CEFDINIR HANMI PHARMACEUTICAL CO., LTD. (KR) 1997-07-10 — — 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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