Cefotaxime

Cefotaxime

SCHEMBL15411

CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(COC(C)=O)CS[C@H]12)c1csc(N)n1

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 Cefotaxime. 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
NR1I2 O75469 6/20 1.00
MAPT P10636 3/20 1.00
PPARG P37231 2/20 1.00
SLC22A6 Q4U2R8 2/20 1.00
SLC22A8 Q8TCC7 2/20 1.00
SLC22A11 Q9NSA0 2/20 1.00
ALB P02768 1/20 1.00
HTR2C P28335 1/20 0.87
TDP1 Q9NUW8 6/20 0.86
APEX1 P27695 3/20 0.86
ABCC4 O15439 2/20 0.86
HSD17B10 Q99714 2/20 0.86
LMNA P02545 2/20 0.86
L3MBTL1 Q9Y468 2/20 0.86
CYP1A2 P05177 1/20 0.86
PKM P14618 1/20 0.86
ALDH1A1 P00352 1/20 0.86
POLB P06746 1/20 0.86
RECQL P46063 1/20 0.86
NPSR1 Q6W5P4 1/20 0.86

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
Cefotaxime SCHEMBL10748430 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL17422140 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL2220120 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL1583477 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL10337429 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL3731937 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL3731931 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL5441797 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL9682785 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL16072837 1.00 NR1I2 (1.00) NR1I2MAPTPPARGSLC22A6SLC22A8

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 45953 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-122071712-A Beta-lactam antibiotic whole-cell biosensor, construction method and application 中国科学院天津工业生物技术研究所 2026-05-22 CN 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-4743580-A1 EFFICIENT TRANSGENE-FREE GENOME EDITING IN PLANTS IN THE T0 GENERATION BASED ON A CO-EDITING STRATEGY University of Florida Research Foundation, Incorporated (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
CN-118304316-B Application of cladribine in preparation of drug for inhibiting growth of multi-drug resistant klebsiella pneumoniae 华南农业大学 2026-05-15 CN 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
EP-4739326-A2 PRODUCTION & SECRETION OF AUXIN-LIKE MOLECULES IN BACTERIA SNIPR Biome ApS (DK) 2026-05-13 EP claimed
US-12622919-B2 Methods for treating hypervirulent Klebsiella pneumoniae infection CITY UNIVERSITY OF HONG KONG (CN) 2026-05-12 US claimed
EP-4736859-A1 ANTIBIOTIC COMPOSITIONS University of Galway (IE) 2026-05-06 EP 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-0083977-A1 6-Alpha-hydroxymethylpenicillanic acid sulfone as a beta-lactamase inhibitor PFIZER INC. (US) 1983-07-20 EP claimed
EP-0074783-A1 Beta-lactamase inhibiting 2-beta-substituted-2-alpha-methyl-(5R) penam-3-alpha-carboxylic acid 1,1-dioxides and intermediates therefor PFIZER INC. (US) 1983-03-23 EP claimed
WO-1982003090-A1 METHOD AND KIT FOR IDENTIFICATION OF BETA-LACTAMASES JAMES RICHARD 1982-09-16 WO claimed
EP-0059645-A1 Method and kit for identification of beta-lactamases NATIONAL RESEARCH DEVELOPMENT CORPORATION (GB) 1982-09-08 EP claimed
EP-0050965-A1 Beta-lactamase inhibitory composition Takeda Chemical Industries, Ltd. (JP) 1982-05-05 EP claimed
EP-0036534-A1 An orally administrable drug form comprising a beta-lactam antibiotic and an adjuvant INTERx RESEARCH CORPORATION (US) 1981-09-30 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
US-4144391-A REPLACING AN ACETOXY GROUP BY A SULFUR NUCLEOPHILE ELI LILLY AND COMPANY (US) 1979-03-13 US claimed