SCHEMBL2539991

SCHEMBL2539991

CC(=O)Oc1ccc(C(=O)COS(=O)(=O)c2ccc(C)cc2)cc1

nearest known ligand 0.54

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.54
STAT3 P40763 1/20 0.51
PKM P14618 2/20 0.50
MAPT P10636 2/20 0.50
POLB P06746 1/20 0.50
ALDH1A1 P00352 4/20 0.48
KMT2A Q03164 3/20 0.45
ENPP1 P22413 2/20 0.43
PTGS2 P35354 1/20 0.43
ENPP3 O14638 1/20 0.43
ENPP2 Q13822 1/20 0.43
ELANE P08246 1/20 0.42
MEN1 O00255 1/20 0.41
HSD17B10 Q99714 1/20 0.41
NPC1 O15118 2/20 0.40
RAB9A P51151 2/20 0.40
RECQL P46063 1/20 0.40

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
SCHEMBL2545038 0.89 STAT3 (0.61) LMNASTAT3PKMMAPTALDH1A1
SCHEMBL2536871 0.86 MAPT (0.54) LMNASTAT3MAPTALDH1A1KMT2A
SCHEMBL15675427 0.83 ALDH1A1 (0.59) LMNASTAT3PKMMAPTALDH1A1
SCHEMBL2542303 0.82 KMT2A (0.59) LMNASTAT3PKMMAPTPOLB
SCHEMBL2537406 0.82 KMT2A (0.59) STAT3PKMMAPTALDH1A1KMT2A
SCHEMBL1089246 0.81 RECQL (0.60) LMNASTAT3MAPTALDH1A1KMT2A
SCHEMBL3472672 0.81 LMNA (0.57) LMNASTAT3PKMMAPTPOLB
SCHEMBL2536867 0.80 MAPT (0.50) LMNAPKMMAPTPOLBALDH1A1
SCHEMBL10777025 0.80 STAT3 (0.52) LMNASTAT3PKMMAPTALDH1A1
SCHEMBL2544896 0.79 AR (0.55) LMNASTAT3MAPTALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8044245-B2 Method for the preparation of optically active 2-sulfonyloxy-1-phenylethanol derivatives KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2011-10-25 US disclosed
US-20100063317-A1 METHOD FOR THE PREPARATION OF OPTICALLY ACTIVE 2-SULFONYLOXY-1-PHENYLETHANOL DERIVATIVES KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2010-03-11 US disclosed
WO-2008054155-A1 METHOD FOR THE PREPARATION OF OPTICALLY ACTIVE 2-SULFONYLOXY-1-PHENYLETHANOL DERIVATIVES KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2008-05-08 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-20100063317-A1 METHOD FOR THE PREPARATION OF OPTICALLY ACTIVE 2-SULFONYLOXY-1-PHENYLETHANOL DERIVATIVES FOXO1, ENO1, SULT1A1 LMNA 4025/4885STAT3 4739/4885PKM 394/4885

“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.