SCHEMBL6679775

SCHEMBL6679775

CC(=O)Oc1ccc(OS(=O)(=O)C(F)(F)F)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.56
POLB P06746 1/20 0.56
PKM P14618 1/20 0.56
LMNA P02545 4/20 0.52
CXCR2 P25025 2/20 0.50
ELANE P08246 1/20 0.50
CXCR1 P25024 1/20 0.49
HSD17B10 Q99714 1/20 0.49
ALDH1A1 P00352 2/20 0.47
GAA P10253 2/20 0.47
HSP90AA1 P07900 1/20 0.47
KDM4E B2RXH2 3/20 0.46
MEN1 O00255 1/20 0.46
TTR P02766 1/20 0.46
TP53 P04637 1/20 0.46
CYP3A4 P08684 1/20 0.46
KMT2A Q03164 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
HSD11B1 P28845 1/20 0.46
TDP1 Q9NUW8 1/20 0.41

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
SCHEMBL12076163 0.83 CYP3A4 (0.53) MAPTPOLBPKMLMNAKDM4E
SCHEMBL576035 0.82 CA2 (0.50) CXCR2CXCR1HSD11B1
SCHEMBL1713127 0.81 STS (0.62) MAPTPOLBLMNACXCR2CXCR1
SCHEMBL1904919 0.81 KDM4E (0.48) MAPTPOLBPKMLMNACXCR2
Acetic Acid SCHEMBL27484648 0.81 CXCR2 (0.49) LMNACXCR2CXCR1MEN1KMT2A
SCHEMBL3668194 0.81 STS (0.60) CXCR2ELANECXCR1HSD11B1STS
SCHEMBL12274397 0.80 MAPT (0.56) MAPTPOLBPKMLMNACXCR2
SCHEMBL1886221 0.80 MAPT (0.65) MAPTPOLBPKMLMNAELANE
SCHEMBL28433059 0.80 CXCR2 (0.46) LMNACXCR2ELANECXCR1ALDH1A1
SCHEMBL6978268 0.79 HSD11B1 (0.48) MAPTPOLBPKMLMNACXCR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240158424-A1 METHOD FOR PRODUCING DIPHOSPHINE MONOXIDE TAKASAGO INTERNATIONAL CORPORATION (JP) 2024-05-16 US disclosed
EP-4361162-A2 METHOD FOR PRODUCING DIPHOSPHINE MONOXIDE Takasago International Corporation (JP) 2024-05-01 EP disclosed
EP-2885288-A1 1,4-DISUBSTITUTED PYRIDAZINE ANALOGS AND METHODS FOR TREATING SMN-DEFICIENCY-RELATED CONDITIONS Novartis AG (CH) 2015-06-24 EP disclosed
WO-2014028459-A1 1,4-DISUBSTITUTED PYRIDAZINE ANALOGS AND METHODS FOR TREATING SMN-DEFICIENCY-RELATED CONDITIONS NOVARTIS AG (CH) 2014-02-20 WO disclosed
WO-2004045610-A1 AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA-3 ADRENERGIC RECEPTOR AGONISTS FUJISAWA PHARMACEUTICAL CO., LTD (JP) 2004-06-03 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 (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-20240158424-A1 METHOD FOR PRODUCING DIPHOSPHINE MONOXIDE TDO2, SCO2, DUOX1 MAPT 4500/4885POLB 296/4885PKM 3091/4885

“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.