Cefotaxime

Cefotaxime

SCHEMBL1279697

CO/N=C(/C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(COC(C)=O)CS[C@H]12)c1csc(N)n1.CO[C@@]1(NC(=O)Cc2cccs2)C(=O)N2C(C(=O)O)=C(COC(N)=O)CS[C@@H]21

nearest known ligand 0.68

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
MAPT P10636 7/20 0.68
NR1I2 O75469 7/20 0.68
PPARG P37231 3/20 0.68
SLC22A6 Q4U2R8 3/20 0.68
SLC22A8 Q8TCC7 3/20 0.68
SLC22A11 Q9NSA0 3/20 0.68
ALB P02768 1/20 0.68
TDP1 Q9NUW8 8/20 0.60
HSD17B10 Q99714 5/20 0.60
APEX1 P27695 3/20 0.60
POLB P06746 2/20 0.60
ALDH1A1 P00352 2/20 0.60
ABCC4 O15439 2/20 0.60
CYP1A2 P05177 1/20 0.60
PKM P14618 1/20 0.60
LMNA P02545 1/20 0.60
RECQL P46063 1/20 0.60
NPSR1 Q6W5P4 1/20 0.60
L3MBTL1 Q9Y468 1/20 0.60
HTR2C P28335 1/20 0.60

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
Cefoxitin SCHEMBL9450006 0.88 NR1I2 (0.81) MAPTNR1I2PPARGSLC22A6SLC22A8
Ceftazidime SCHEMBL6698665 0.86 NR1I2 (0.66) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefoxitin SCHEMBL11165402 0.83 NR1I2 (0.73) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL10337429 0.83 NR1I2 (1.00) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL1583477 0.83 NR1I2 (1.00) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL16072837 0.83 NR1I2 (1.00) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL5441797 0.83 NR1I2 (1.00) MAPTNR1I2PPARGSLC22A6SLC22A8
SCHEMBL9660046 0.83 NR1I2 (0.88) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL17422140 0.83 NR1I2 (1.00) MAPTNR1I2PPARGSLC22A6SLC22A8
Cefotaxime SCHEMBL3731937 0.83 NR1I2 (1.00) MAPTNR1I2PPARGSLC22A6SLC22A8

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120088769-A1 SALTS OF ARYLSULFONAMIDE CCR3 ANTAGONISTS AXIKIN PHARMACEUTICALS, INC. (US) 2012-04-12 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 (1 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-20120088769-A1 SALTS OF ARYLSULFONAMIDE CCR3 ANTAGONISTS CCR3, CCR1, CCR4 MAPT 3729/4885NR1I2 107/4885PPARG 2322/4885

“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.