SCHEMBL5445969

SCHEMBL5445969

COC(=O)c1ccsc1-c1ccc(N)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS1 P23219 1/20 0.48
GAA P10253 3/20 0.47
KMT2A Q03164 4/20 0.45
SMN1; SMN2 Q16637 3/20 0.45
MEN1 O00255 2/20 0.45
KDM4E B2RXH2 6/20 0.43
ALDH1A1 P00352 6/20 0.43
HSD17B10 Q99714 4/20 0.43
CFTR P13569 1/20 0.43
ATM Q13315 2/20 0.42
POLB P06746 2/20 0.42
PKM P14618 2/20 0.41
TP53 P04637 1/20 0.41
MDM2 Q00987 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
MAPT P10636 3/20 0.41
HPGD P15428 3/20 0.41
GLA P06280 1/20 0.40
CASP1 P29466 1/20 0.40
CASP7 P55210 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
SCHEMBL17010936 0.90 PTGS1 (0.53) PTGS1KMT2ASMN1; SMN2MEN1KDM4E
SCHEMBL5445652 0.85 PTGS1 (0.49) PTGS1KMT2ASMN1; SMN2MEN1KDM4E
SCHEMBL14564435 0.85 ALDH1A1 (0.49) PTGS1KMT2ASMN1; SMN2MEN1KDM4E
SCHEMBL3321379 0.83 KDM4E (0.56) PTGS1GAAKMT2ASMN1; SMN2MEN1
SCHEMBL5949785 0.81 ALDH1A1 (0.50) GAAKMT2ASMN1; SMN2MEN1KDM4E
SCHEMBL15775647 0.80 SLC6A3 (0.53) PTGS1KMT2ASMN1; SMN2MEN1KDM4E
SCHEMBL5454754 0.78 SLC6A3 (0.50) PTGS1GAAKMT2ASMN1; SMN2MEN1
SCHEMBL4952543 0.77 ALDH1A1 (0.55) PTGS1GAAKMT2AMEN1ALDH1A1
SCHEMBL190088 0.77 KMT2A (0.59) GAAKMT2ASMN1; SMN2MEN1KDM4E
SCHEMBL24421257 0.76 KMT2A (0.47) PTGS1GAAKMT2ASMN1; SMN2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070054902-A1 Isoxazole derivatives as peroxisome proliferator-activated receptors agonists SHIONOGI & CO., LTD. (JP) 2007-03-08 US disclosed
US-20070054902-A1 Isoxazole derivatives as peroxisome proliferator-activated receptors agonists SHIONOGI & CO., LTD. (JP) 2007-03-08 US disclosed
US-20070054902-A1 Isoxazole derivatives as peroxisome proliferator-activated receptors agonists SHIONOGI & CO., LTD. (JP) 2007-03-08 US disclosed
EP-1690538-A1 ISOXAZOLE DERIVATIVE HAVING AGONISTIC ACTIVITY AGAINST PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR SHIONOGI & CO., LTD. (JP) 2006-08-16 EP disclosed
US-20060148887-A1 Chemical compounds OXFORD FINANCE LLC, AS COLLATERAL AGENT 2006-07-06 US disclosed
US-7034053-B2 Phenethanolamine derivatives, compositions, and their use as agonists at atypical beta-adrenoreceptors SMITHKLINE BEECHAM CORPORATION (US) 2006-04-25 US disclosed
EP-1366033-B1 CHEMICAL COMPOUNDS GLAXO GROUP LTD (GB) 2005-04-27 EP disclosed
US-20040106672-A1 beta-adrenoceptor agonist for the prevention or treatment of obesity; Suitable compounds of formula (I) of the invention include:2-(3-{2R-[2-(3-Chlorophenyl)-2R-hydroxyl-ethylamino]propylamino}phenyl)furan-3-carboxylic acid B3AR THERAPEUTICS, INC. 2004-06-03 US disclosed
CN-1487928-A Compound (I) 2004-04-07 CN disclosed
EP-1366033-A1 CHEMICAL COMPOUNDS GLAXO GROUP LIMITED (GB) 2003-12-03 EP disclosed
WO-2002060885-A1 CHEMICAL COMPOUNDS GLAXO GROUP LIMITED (GB) 2002-08-08 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 (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-20040106672-A1 beta-adrenoceptor agonist for the prevention or treatment of obesity; Suitable compounds of formula (I) of the invention include:2-(3-{2R-[2-(3-Chlorophenyl)-2R-hydroxyl-ethylamino]propylamino}phenyl)furan-3-carboxylic acid ADRB3, ADRB1, ADRB2 PTGS1 807/4885GAA 1104/4885KMT2A 3023/4885
US-20060148887-A1 Chemical compounds ADRB3, GPR119, ADRB1 PTGS1 299/4885GAA 740/4885KMT2A 4122/4885
US-20070054902-A1 Isoxazole derivatives as peroxisome proliferator-activated receptors agonists NR1H3, NR1H2, RXRA PTGS1 2416/4885GAA 4411/4885KMT2A 3046/4885

“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.