SCHEMBL21723987

SCHEMBL21723987

COc1ccc(-c2cc3c(s2)c(-c2ccc(OC)cc2)cc(=O)n3C)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 8/20 0.48
RAB9A P51151 8/20 0.48
KDM4E B2RXH2 5/20 0.48
PKM P14618 3/20 0.48
ALDH1A1 P00352 4/20 0.45
SMN1; SMN2 Q16637 4/20 0.45
HPGD P15428 3/20 0.45
PDPK1 O15530 1/20 0.45
HSD17B10 Q99714 3/20 0.43
TP53 P04637 2/20 0.43
MAPT P10636 2/20 0.43
ALOX15 P16050 1/20 0.43
TSHR P16473 1/20 0.43
NFKB1 P19838 1/20 0.43
MAPK1 P28482 1/20 0.43
NFKB2 Q00653 1/20 0.43
RELA Q04206 1/20 0.43
APP P05067 1/20 0.42
HTT P42858 1/20 0.42
KMT2A Q03164 3/20 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
SCHEMBL21723639 0.95 HSD17B10 (0.47) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL21723934 0.91 NPC1 (0.42) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL21723952 0.89 GSK3B (0.41) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL21723989 0.86 NPC1 (0.48) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL25259095 0.84 KDM4E (0.37) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL23452001 0.82 LMNA (0.43) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL23451957 0.81 GABRG2 (0.46) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL25297318 0.78 NPC1 (0.40) NPC1RAB9AKDM4EALDH1A1SMN1; SMN2
SCHEMBL21723705 0.78 NPC1 (0.51) NPC1RAB9AKDM4EPKMALDH1A1
SCHEMBL21723978 0.74 HSD17B10 (0.44) NPC1RAB9AKDM4EPKMALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12415813-B2 Method for synthesizing thieno[3,2-b]pyridine-5(4H)-one derivative compound, using gold catalyst, and use therefor KOREA INSTITUTE OF OCEAN SCIENCE & TECHNOLOGY (KR) 2025-09-16 US disclosed
US-20210332063-A1 METHOD FOR SYNTHESIZING THIENO[3,2-B]PYRIDINE-5(4H)-ONE DERIVATIVE COMPOUND, USING GOLD CATALYST, AND USE THEREFOR KOREA INSTITUTE OF OCEAN SCIENCE & TECHNOLOGY (KP) 2021-10-28 US disclosed
US-20210332063-A1 METHOD FOR SYNTHESIZING THIENO[3,2-B]PYRIDINE-5(4H)-ONE DERIVATIVE COMPOUND, USING GOLD CATALYST, AND USE THEREFOR KOREA INSTITUTE OF OCEAN SCIENCE & TECHNOLOGY (KP) 2021-10-28 US disclosed
WO-2020036243-A1 METHOD FOR SYNTHESIZING THIENO[3,2-B]PYRIDINE-5(4H)-ONE DERIVATIVE COMPOUND, USING GOLD CATALYST, AND USE THEREFOR 한국해양과학기술원 2020-02-20 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 (2 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-20210332063-A1 METHOD FOR SYNTHESIZING THIENO[3,2-B]PYRIDINE-5(4H)-ONE DERIVATIVE COMPOUND, USING GOLD CATALYST, AND USE THEREFOR FARS2, CYP4F11, CYP4B1 NPC1 3352/4885RAB9A 3000/4885KDM4E 1113/4885
US-12415813-B2 Method for synthesizing thieno[3,2-b]pyridine-5(4H)-one derivative compound, using gold catalyst, and use therefor FARS2, CYP4F11, CYP4B1 NPC1 3352/4885RAB9A 3000/4885KDM4E 1113/4885

“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.