Cefadroxil

Cefadroxil

SCHEMBL3984780

CC1=C(C(=O)O)N2C(=O)C(NC(=O)C(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 Cefadroxil. 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
MAPT P10636 8/20 1.00
HSD17B10 Q99714 7/20 1.00
KMT2A Q03164 6/20 1.00
MEN1 O00255 5/20 1.00
SLC15A2 Q16348 3/20 1.00
LMNA P02545 2/20 1.00
ESR1 P03372 1/20 1.00
SLC22A6 Q4U2R8 1/20 1.00
SLC22A8 Q8TCC7 1/20 1.00
ALDH1A1 P00352 7/20 0.85
CYP3A4 P08684 4/20 0.85
HPGD P15428 3/20 0.85
TDP1 Q9NUW8 3/20 0.85
BLM P54132 2/20 0.85
CYP2C19 P33261 2/20 0.85
MAPK1 P28482 1/20 0.85
ADRA1A P35348 1/20 0.85
HTR2B P41595 1/20 0.85
PTGS2 P35354 2/20 0.75
DRD2 P14416 1/20 0.75

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
Cefadroxil SCHEMBL6438517 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL16072813 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL3984782 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL524155 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL19123520 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL151320 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL9650920 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL13698957 1.00 MAPT (1.00) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL9807365 0.99 MAPT (0.98) MAPTHSD17B10KMT2AMEN1SLC15A2
Cefadroxil SCHEMBL1821440 0.99 MAPT (0.98) MAPTHSD17B10KMT2AMEN1SLC15A2

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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE31730-E Process for the preparation of the crystalline monohydrate of 7-(D-α-aα-(p-hydroxyphenyl)acetamido)-3-methyl-3-cephem-4-carboxylic acid BRISTOL-MYERS COMPANY (US) 1984-11-13 US claimed
US-4391974-A LYSINE SALT, CEPHALOSPORINS LIOFILIZACIONES ESTERILIZACIONES Y SINTHESIS S.A. (ES) 1983-07-05 US claimed
US-4234721-A Process for the preparation of the crystalline monohydrate of 7-[D-amino-(p-hydroxyphenyl]acetamido)-3-methyl-3-cephen-4-carboxylic acid BRISTOL-MYERS COMPANY (US) 1980-11-18 US claimed
US-4160863-A ANTIBIOTIC BRISTOL-MYERS COMPANY (US) 1979-07-10 US claimed
US-20090221815-A1 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CJ CHEILJEDANG CORPORATION (KR) 2009-09-03 US disclosed
US-7544797-B2 Processes for the preparation of cephem derivatives CJ CHEILJEDANG CORPORATION (KR) 2009-06-09 US disclosed
US-20070060747-A1 Processes for the preparation of cephem derivatives CJ CORPORATION (KR) 2007-03-15 US disclosed
WO-2004035593-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF CEFADROXIL ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2004-04-29 WO disclosed
US-20040077849-A1 Process for the preparation of cefadroxil ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2004-04-22 US disclosed
US-6337396-B1 CEPHALOSPORIN ANTIBIOTICS RANBAXY LABORATORIES LIMITED (IN) 2002-01-08 US disclosed
EP-0690864-B1 CRYSTALLINE CEFTIOFUR FREE ACID UPJOHN CO (US) 2001-06-13 EP disclosed
EP-0690864-A1 CRYSTALLINE CEFTIOFUR FREE ACID PHARMACIA & UPJOHN COMPANY (US) 1996-01-10 EP disclosed
EP-0000393-A1 Beta-lactam compounds, process for their preparation and their use BAYER AG (DE) 1979-01-24 EP disclosed
US-4107304-A Oxo-imidazolidine substituted cephalosporins and antibacterial compositions and methods of combatting bacteria employing them BAYER AKTIENGESELLSCHAFT (DE) 1978-08-15 US disclosed
US-4093722-A ANTIBIOTICS BAYER AKTIENGESELLSCHAFT (DT) 1978-06-06 US disclosed
US-4086340-A ANTIBIOTIC; ANIMAL GROWTH PROMOTER BAYER AKTIENGESELLSCHAFT (DT) 1978-04-25 US disclosed
US-4086341-A NITRO SUBSTITUTED; ANTIBIOTIC BAYER AKTIENGESELLSCHAFT (DT) 1978-04-25 US disclosed
US-4029806-A Nitro-β-lactam antibiotics and processes for their preparation and use BAYER AKTIENGESELLSCHAFT (DT) 1977-06-14 US disclosed
US-4012518-A PENICILLIN DERIVATIVES AS GROWTH AND FEED UTILIZATION PROMOTERS IN ANIMALS BAYER AKTIENGESELLSCHAFT (DT) 1977-03-15 US disclosed
US-3985741-A Production of p-hydroxycephalexin BRISTOL-MYERS COMPANY (US) 1976-10-12 US disclosed

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

For each of this compound's patents that has machine-readable text (3 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-20070060747-A1 Processes for the preparation of cephem derivatives CEP170, HAMP, NISCH MAPT 1430/4885HSD17B10 1307/4885KMT2A 2733/4885
US-20040077849-A1 Process for the preparation of cefadroxil CFD, CYP2F1, CYP2W1 MAPT 4152/4885HSD17B10 519/4885KMT2A 3271/4885
US-20090221815-A1 PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES CEP170, HAMP, NISCH MAPT 1430/4885HSD17B10 1307/4885KMT2A 2733/4885

“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.