SCHEMBL14765167

SCHEMBL14765167

CC(=O)c1cc[n+](C)cc1.COS(=O)(=O)[O-]

nearest known ligand 0.43

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3

The experimentally established mechanism targets of None. 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
STS P08842 1/20 0.40
MAPT P10636 3/20 0.38
HPGD P15428 3/20 0.38
RAB9A P51151 2/20 0.38
APOBEC3A P31941 3/20 0.38
APOBEC3G Q9HC16 3/20 0.38
PABPC1 P11940 1/20 0.38
EIF4H Q15056 1/20 0.38
USP2 O75604 1/20 0.37
NPC1 O15118 1/20 0.37
ALDH1A1 P00352 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
KMT2A Q03164 3/20 0.36
MEN1 O00255 2/20 0.36
CA12 O43570 2/20 0.36
CA9 Q16790 2/20 0.36
MAPK1 P28482 1/20 0.35
LMNA P02545 2/20 0.35
CA1 P00915 1/20 0.35
CA2 P00918 1/20 0.35

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
SCHEMBL6553185 0.87 USP2 (0.40) STSMAPTHPGDRAB9AAPOBEC3A
Sulfuric Acid SCHEMBL140508 0.87 USP2 (0.40) STSMAPTHPGDRAB9AAPOBEC3A
Sulfuric Acid SCHEMBL140509 0.87 USP2 (0.40) STSMAPTHPGDRAB9AAPOBEC3A
SCHEMBL30505 0.82 HPGD (0.46) MAPTHPGDRAB9AAPOBEC3AAPOBEC3G
Acetic Acid SCHEMBL145430 0.81 MAPK1 (0.47) MAPTHPGDRAB9AAPOBEC3AAPOBEC3G
Hydrochloric Acid SCHEMBL152518 0.80 HPGD (0.44) MAPTHPGDRAB9AAPOBEC3AAPOBEC3G
Bromide SCHEMBL145328 0.80 HPGD (0.44) MAPTHPGDRAB9AAPOBEC3AAPOBEC3G
Iodide SCHEMBL10670645 0.80 APOBEC3A (0.46) MAPTHPGDRAB9AAPOBEC3AAPOBEC3G
SCHEMBL1712117 0.80 HPGD (0.44) MAPTHPGDRAB9AAPOBEC3AAPOBEC3G
Paraquat SCHEMBL3676472 0.79 SLC6A4 (0.48) APOBEC3AAPOBEC3GPABPC1EIF4H

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2753620-B1 NOVEL PROCESS FOR PREPARING CEFTAROLINE FOSAMIL SANDOZ AG (CH) 2017-02-15 EP disclosed
US-9382278-B2 Process for preparing ceftaroline fosamil SANDOZ AG (CH) 2016-07-05 US disclosed
US-20160009745-A1 NOVEL PROCESS FOR PREPARING CEFTAROLINE FOSAMIL SANDOZ AG (CH) 2016-01-14 US disclosed
US-9169239-B2 Process for preparing ceftaroline fosamil SANDOZ AG (CH) 2015-10-27 US disclosed
US-20150073138-A1 NOVEL PROCESS FOR PREPARING CEFTAROLINE FOSAMIL SANDOZ AG (CH) 2015-03-12 US disclosed
WO-2013034718-A1 NOVEL PROCESS FOR PREPARING CEFTAROLINE FOSAMIL SANDOZ AG (CH) 2013-03-14 WO 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 (2 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-20150073138-A1 NOVEL PROCESS FOR PREPARING CEFTAROLINE FOSAMIL FOS, FOSB, CYP3A7 STS 1134/4885MAPT 4496/4885HPGD 3071/4885
US-20160009745-A1 NOVEL PROCESS FOR PREPARING CEFTAROLINE FOSAMIL FOS, FOSB, CYP3A7 STS 981/4885MAPT 4497/4885HPGD 3453/4885

“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.