SCHEMBL4126633

SCHEMBL4126633

COC(=O)Cc1cccnc1Cl

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
P2RX7 Q99572 1/20 0.45
CASP3 P42574 2/20 0.44
SENP8 Q96LD8 2/20 0.44
SENP7 Q9BQF6 2/20 0.44
SENP6 Q9GZR1 2/20 0.44
SMN1; SMN2 Q16637 4/20 0.43
LMNA P02545 2/20 0.43
ALDH1A1 P00352 3/20 0.41
HSP90AA1 P07900 1/20 0.41
POLB P06746 2/20 0.41
RAB9A P51151 3/20 0.40
NPC1 O15118 2/20 0.40
FAAH O00519 1/20 0.40
HTT P42858 3/20 0.40
KDM4E B2RXH2 2/20 0.40
CYP1A2 P05177 1/20 0.40
MAPT P10636 1/20 0.40
PKM P14618 1/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 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
SCHEMBL28121426 0.85 CASP3 (0.46) P2RX7CASP3SENP8SENP7SENP6
SCHEMBL3587106 0.84 MAPT (0.46) CASP3SENP8SENP7SENP6LMNA
SCHEMBL20565261 0.83 POLB (0.47) P2RX7CASP3SENP8SENP7SENP6
SCHEMBL21522559 0.81 PDCD1 (0.44) P2RX7CASP3SENP8SENP7SENP6
SCHEMBL22028701 0.81 KDM4E (0.41) SMN1; SMN2LMNAALDH1A1RAB9AKDM4E
SCHEMBL14678422 0.81 P2RX7 (0.47) P2RX7SMN1; SMN2LMNAALDH1A1RAB9A
SCHEMBL3110927 0.81 SMN1; SMN2 (0.47) P2RX7CASP3SENP8SENP7SENP6
SCHEMBL14267784 0.80 KDM4E (0.40) SMN1; SMN2LMNAALDH1A1POLBRAB9A
SCHEMBL18481212 0.80 MAPT (0.42) CASP3SENP8SENP7SENP6SMN1; SMN2
SCHEMBL8998233 0.80 KDM4E (0.43) SMN1; SMN2LMNAALDH1A1RAB9AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104513194-A 2-chloro-3-aldehyde pyridine synthetic method NANJING RED SUN CO LTD 2015-04-15 CN claimed
US-12459942-B2 Inhibiting (α-v)(β-6) integrin MORPHIC THERAPEUTIC, INC. (US) 2025-11-04 US disclosed
US-20240376095-A1 INHIBITING (ALPHA-V)(BETA-6) INTEGRIN SCHR¿DINGER, LLC 2024-11-14 US disclosed
US-12139462-B2 Pyridinone MK2 inhibitors and uses thereof XINTHERA, INC. (US) 2024-11-12 US disclosed
CN-118878533-A Inhibition of αvβ6 integrin 莫菲克医疗股份有限公司 2024-11-01 CN disclosed
US-20240300951-A1 Pyrazolopyridinone Compounds BEIGENE LTD. (KY) 2024-09-12 US disclosed
US-20240270751-A1 Pyrazolopyridinone Compounds BEIGENE LTD. (KY) 2024-08-15 US disclosed
CN-112805001-B Inhibition of αvβ6 integrin 莫菲克医疗股份有限公司 2024-07-23 CN disclosed
EP-4367099-A1 PYRIDINONE MK2 INHIBITORS AND USES THEREOF Xinthera, Inc. (US) 2024-05-15 EP disclosed
CN-117836296-A Pyrazolopyridone compounds 百济神州有限公司 2024-04-05 CN disclosed
US-20080064691-A1 Heterocyclic Amide Derivatives Which Possess Glycogen Phosphorylase Inhibitory Activity ASTRAZENECA AB (SE) 2008-03-13 US disclosed
WO-2007088345-A1 THIENO-PYRIDINE DERIVATIVES AS MEK INHIBITORS UCB PHARMA S.A. (BE) 2007-08-09 WO disclosed
EP-0312243-B1 Methyl 2-[2-(3-substituted phenoxy)pyridin-3-yl]-3-methoxypropenoatesand their use as fungicides ZENECA LTD (GB) 1996-08-07 EP disclosed
US-5198444-A Methyl α-(2-substituted)pyrid-3-yl-β-methoxyacrylates, compositions containing them and their use as fungicides IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1993-03-30 US disclosed
US-5158954-A For agriculture IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-10-27 US disclosed
EP-0312221-B1 CHEMICAL PROCESS FOR THE PREPARATION OF METHYL 2-(3-PHENOXYPYRID-2-YL)-3-PROPENOATES IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-10-21 EP disclosed
US-5039810-A Pyridyl propenoate compound IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-08-13 US disclosed
US-5008276-A Plants IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-04-16 US disclosed
EP-0312243-A2 Methyl 2-[2-(3-substituted phenoxy)pyridin-3-yl]-3-methoxypropenoatesand their use as fungicides ZENECA LIMITED (GB) 1989-04-19 EP disclosed
EP-0312221-A2 Chemical process for the preparation of methyl 2-(3-phenoxypyrid-2-yl)-3-propenoates IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-04-19 EP 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 (6 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-12139462-B2 Pyridinone MK2 inhibitors and uses thereof ENPP2, PLP2, PDXK P2RX7 1226/4885CASP3 3188/4885SENP8 3851/4885
US-12459942-B2 Inhibiting (α-v)(β-6) integrin ITGB6, ITGA6, ITGAV P2RX7 2117/4885CASP3 1864/4885SENP8 3628/4885
US-20240376095-A1 INHIBITING (ALPHA-V)(BETA-6) INTEGRIN ITGB6, ITGA6, ITGAV P2RX7 2267/4885CASP3 1848/4885SENP8 3732/4885
US-20240300951-A1 Pyrazolopyridinone Compounds NFATC1, CD4, PBK P2RX7 337/4885CASP3 315/4885SENP8 2584/4885
US-20240270751-A1 Pyrazolopyridinone Compounds NFATC1, CD4, PBK P2RX7 337/4885CASP3 315/4885SENP8 2584/4885
US-20080064691-A1 Heterocyclic Amide Derivatives Which Possess Glycogen Phosphorylase Inhibitory Activity PYGL, PYGM, GYS1 P2RX7 2472/4885CASP3 2502/4885SENP8 3512/4885

“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.