SCHEMBL4949422

SCHEMBL4949422

N#Cc1ccsc1C(=O)O

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.43
NPSR1 Q6W5P4 2/20 0.43
POLB P06746 2/20 0.43
RAB9A P51151 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
PTPN2 P17706 1/20 0.43
PTPN1 P18031 1/20 0.43
AXL P30530 1/20 0.42
MEN1 O00255 5/20 0.41
KMT2A Q03164 5/20 0.41
HPGD P15428 1/20 0.41
BLM P54132 1/20 0.41
KDM4E B2RXH2 3/20 0.40
ALDH1A1 P00352 2/20 0.40
MAPT P10636 3/20 0.39
GAA P10253 2/20 0.39
RECQL P46063 1/20 0.39
GPR35 Q9HC97 1/20 0.39
PTPRC P08575 1/20 0.39
ALOX15 P16050 2/20 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
SCHEMBL24577695 0.83 LMNA (0.39) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL3056218 0.82 KDM4E (0.42) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL506452 0.82 KDM4E (0.41) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL5868810 0.80 LMNA (0.45) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL22031739 0.79 GPR35 (0.46) LMNANPSR1RAB9APTPN2PTPN1
SCHEMBL12622649 0.79 POLB (0.52) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL4404656 0.75 DHODH (0.43) LMNANPSR1RAB9APTPN2PTPN1
SCHEMBL9116385 0.75 LMNA (0.36) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL9116375 0.75 LMNA (0.36) LMNANPSR1POLBRAB9ASMN1; SMN2
SCHEMBL21554150 0.74 GAA (0.42) LMNANPSR1POLBRAB9ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230309388-A1 ORGANIC ELECTROLUMINESCENT MATERIAL AND DEVICE Beijing Summer Sprout Technology Co., Ltd. (CN) 2023-09-28 US disclosed
US-9029499-B2 Semiconducting polymers UNIVERSITY OF CHICAGO (US) 2015-05-12 US disclosed
US-9029499-B2 Semiconducting polymers UNIVERSITY OF CHICAGO (US) 2015-05-12 US disclosed
EP-2307483-B1 SEMICONDUCTING POLYMERS UNIV CHICAGO (US) 2015-04-22 EP disclosed
US-20140235817-A1 SEMICONDUCTING POLYMERS UNIVERSITY OF CHICAGO (US) 2014-08-21 US disclosed
US-20140235817-A1 SEMICONDUCTING POLYMERS UNIVERSITY OF CHICAGO (US) 2014-08-21 US disclosed
US-8653228-B2 Semiconducting polymers UNIVERSITY OF CHICAGO (US) 2014-02-18 US disclosed
US-8653228-B2 Semiconducting polymers UNIVERSITY OF CHICAGO (US) 2014-02-18 US disclosed
US-8436134-B2 Semiconducting polymers UNIVERSITY OF CHICAGO (US) 2013-05-07 US disclosed
US-20110124822-A1 SEMICONDUCTING POLYMERS NATIONAL SCIENCE FOUNDATION 2011-05-26 US disclosed
US-7041685-B2 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. (US) 2006-05-09 US disclosed
US-20050154012-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2005-07-14 US disclosed
EP-1406632-A2 SUBSTITUTED 3-ARYL-5-ARYL- 1,2,4]-OXADIAZOLES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF Cytovia, Inc. (US) 2004-04-14 EP disclosed
US-20030045546-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2003-03-06 US disclosed
WO-2002100826-A2 SUBSTITUTED 3-ARYL-5-ARYL-[1,2,4]-OXADIAZOLES AND ANALOGS CYTOVIA, INC. (US) 2002-12-19 WO disclosed
US-5840917-A ADMINISTERING TO MAMMAL TO ERADICATE HELICOBACTER PYLORI TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1998-11-24 US disclosed
WO-1998042347-A1 PHARMACEUTICAL COMPOSITION CONTAINING A PHOSPHORYLAMIDE AND AN AYNTIBIOTIC TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1998-10-01 WO disclosed
EP-0852498-A1 PHOSPHORYLAMIDES, THEIR PREPARATION AND USE Takeda Chemical Industries, Ltd. (JP) 1998-07-15 EP disclosed
WO-1997011705-A1 PHOSPHORYLAMIDES, THEIR PREPARATION AND USE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1997-04-03 WO disclosed
US-4025505-A ANTICONVULSANTS CIBA-GEIGY CORPORATION (US) 1977-05-24 US 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-20030045546-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CASP3, CASP1, API5 LMNA 1419/4885NPSR1 4000/4885POLB 2836/4885
US-20230309388-A1 ORGANIC ELECTROLUMINESCENT MATERIAL AND DEVICE OCIAD1, OCIAD2, SLCO4C1 LMNA 2062/4885NPSR1 4548/4885POLB 2113/4885
US-20050154012-A1 Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof CASP3, CASP1, CASP4 LMNA 1844/4885NPSR1 4405/4885POLB 3317/4885

“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.