SCHEMBL1371646

SCHEMBL1371646

COC(=O)c1sc(Br)cc1OC

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 5/20 0.42
MAPT P10636 3/20 0.42
TSHR P16473 1/20 0.42
HSD17B10 Q99714 1/20 0.42
KDM4E B2RXH2 2/20 0.41
PPARG P37231 1/20 0.39
NCOA1 Q15788 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39
NCOA3 Q9Y6Q9 1/20 0.39
MEN1 O00255 3/20 0.38
ALDH1A1 P00352 2/20 0.38
POLB P06746 2/20 0.38
HPGD P15428 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
MAPK1 P28482 1/20 0.38
TP53 P04637 1/20 0.38
LCK P06239 1/20 0.38
FYN P06241 1/20 0.38
GSK3B P49841 1/20 0.38
CISD2 Q8N5K1 1/20 0.38

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
SCHEMBL22833208 0.83 LCK (0.47) KDM4ENPSR1ALDH1A1HPGDMAPK1
SCHEMBL4337879 0.83 KMT2A (0.54) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL31223040 0.82 NOTUM (0.39) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL319034 0.81 GSK3B (0.53) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL31435566 0.80 KMT2A (0.56) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL8928555 0.79 MAPT (0.46) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL1971697 0.79 MAPT (0.44) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL1374020 0.79 TSHR (0.44) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL2730725 0.79 MAPT (0.44) KMT2AMAPTTSHRHSD17B10KDM4E
SCHEMBL102283 0.78 KDM4E (0.53) KMT2AMAPTTSHRHSD17B10KDM4E

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 42 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4676476-A1 INHIBITORS OF TDP-43 AND TAU AGGREGATION Aquinnah Pharmaceuticals, Inc. (US) 2026-01-14 EP disclosed
WO-2024187126-A1 INHIBITORS OF TDP-43 AND TAU AGGREGATION AQUINNAH PHARMACEUTICALS, INC. (US) 2024-09-12 WO disclosed
US-20230142338-A1 THIOPHENYL DERIVATIVES USEFUL FOR MODULATING NUCLEIC ACID SPLICING REMIX THERAPEUTICS INC. 2023-05-11 US disclosed
US-20220363673-A1 5-(Thiophen-2-YL)-1 H-Tetrazole Derivative as BCKDK Inhibitors Useful for Treating Various Diseases PFIZER INC. (US) 2022-11-17 US disclosed
EP-3990452-A1 5-(THIOPHEN-2-YL)-1H-TETRAZOLE DERIVATIVES AS BCKDK INHIBITORS USEFUL FOR TREATING VARIOUS DISEASES Pfizer Inc. (US) 2022-05-04 EP disclosed
WO-2020261144-A1 5-(THIOPHEN-2-YL)-1H-TETRAZOLE DERIVATIVES AS BCKDK INHIBITORS USEFUL FOR TREATING VARIOUS DISEASES PFIZER INC. (US) 2020-12-30 WO disclosed
US-20150038535-A1 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMA (US) 2015-02-05 US disclosed
US-20150038535-A1 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMA (US) 2015-02-05 US disclosed
US-20150038535-A1 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMA (US) 2015-02-05 US disclosed
US-8853244-B2 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMACEUTICALS INCORPORATED (US) 2014-10-07 US disclosed
US-20080045570-A1 To treat autoimmune, inflammatory, proliferative, hyperproliferative,neurodegenerative or immunologically-mediated diseases; useful for the study of kinases in biological and pathological phenomena; study of intracellular signal transduction pathways mediated by such kinases, and comparative evaluation VERTEX PHARMACEUTICALS INCORPORATED 2008-02-21 US disclosed
US-20080045570-A1 To treat autoimmune, inflammatory, proliferative, hyperproliferative,neurodegenerative or immunologically-mediated diseases; useful for the study of kinases in biological and pathological phenomena; study of intracellular signal transduction pathways mediated by such kinases, and comparative evaluation VERTEX PHARMACEUTICALS INCORPORATED 2008-02-21 US disclosed
US-20080045570-A1 To treat autoimmune, inflammatory, proliferative, hyperproliferative,neurodegenerative or immunologically-mediated diseases; useful for the study of kinases in biological and pathological phenomena; study of intracellular signal transduction pathways mediated by such kinases, and comparative evaluation VERTEX PHARMACEUTICALS INCORPORATED 2008-02-21 US disclosed
WO-2007139816-A2 THIOPHENE-CARBOXAMIDES USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2007-12-06 WO disclosed
WO-2007139816-A2 THIOPHENE-CARBOXAMIDES USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2007-12-06 WO disclosed
US-20070219205-A1 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMACEUTICALS INCORPORATED 2007-09-20 US disclosed
US-20070219205-A1 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMACEUTICALS INCORPORATED 2007-09-20 US disclosed
US-20070219205-A1 Thiophene-carboxamides useful as inhibitors of protein kinases VERTEX PHARMACEUTICALS INCORPORATED 2007-09-20 US disclosed
WO-2007087283-A2 THIOPHENE-CARBOXAMIDES USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2007-08-02 WO disclosed
WO-2007087283-A2 THIOPHENE-CARBOXAMIDES USEFUL AS INHIBITORS OF PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2007-08-02 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 (5 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-20080045570-A1 To treat autoimmune, inflammatory, proliferative, hyperproliferative,neurodegenerative or immunologically-mediated diseases; useful for the study of kinases in biological and pathological phenomena; study of intracellular signal transduction pathways mediated by such kinases, and comparative evaluation MAP3K1, MAP3K20, MAP3K2 KMT2A 2551/4885MAPT 775/4885TSHR 2079/4885
US-20220363673-A1 5-(Thiophen-2-YL)-1 H-Tetrazole Derivative as BCKDK Inhibitors Useful for Treating Various Diseases BCKDK, PDK4, PFKL KMT2A 2827/4885MAPT 3288/4885TSHR 1864/4885
US-20150038535-A1 Thiophene-carboxamides useful as inhibitors of protein kinases MAP3K20, ABL1, MAP3K5 KMT2A 784/4885MAPT 1279/4885TSHR 2596/4885
US-20070219205-A1 Thiophene-carboxamides useful as inhibitors of protein kinases MAP3K20, ABL1, MAP3K5 KMT2A 784/4885MAPT 1279/4885TSHR 2596/4885
US-20230142338-A1 THIOPHENYL DERIVATIVES USEFUL FOR MODULATING NUCLEIC ACID SPLICING SNRPA, NSUN3, NSUN2 KMT2A 2797/4885MAPT 4027/4885TSHR 2637/4885

“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.