SCHEMBL569230

SCHEMBL569230

O=C(O)c1nccnc1Cl

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.48
LMNA P02545 1/20 0.48
KDM4E B2RXH2 7/20 0.45
MAPT P10636 5/20 0.45
ALDH1A1 P00352 4/20 0.45
TSHR P16473 2/20 0.45
CYP3A4 P08684 1/20 0.45
ALOX15 P16050 1/20 0.45
BLM P54132 1/20 0.45
AGER Q15109 1/20 0.45
NPSR1 Q6W5P4 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
ASPH Q12797 1/20 0.42
KDM8 Q8N371 1/20 0.42
CYP1A2 P05177 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
NAPRT Q6XQN6 2/20 0.38
HCAR2 Q8TDS4 2/20 0.38
KMT2A Q03164 2/20 0.37
MEN1 O00255 1/20 0.37

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
SCHEMBL30042917 1.00 SMN1; SMN2 (0.48) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
Hydrochloric Acid SCHEMBL1452738 0.98 LMNA (0.47) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL5684624 0.82 SMN1; SMN2 (0.40) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL20184160 0.82 KDM4E (0.36) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL2041795 0.81 SMN1; SMN2 (0.41) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL69939 0.81 KDM4E (0.54) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL1452735 0.80 SMN1; SMN2 (0.39) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
Water SCHEMBL335807 0.78 KDM4E (0.52) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL6345905 0.78 KDM4E (0.52) SMN1; SMN2LMNAKDM4EMAPTALDH1A1
SCHEMBL29113117 0.78 KDM4E (0.52) SMN1; SMN2LMNAKDM4EMAPTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108079938-A There is the PERFORMANCE OF MODIFIED VERMICULITE adsorbent of absorption property to the orthophosphates in water body 北京益清源环保科技有限公司 2018-05-29 CN claimed
EP-1877401-A2 NOVEL COMPOUNDS USEFUL FOR BRADYKININ B1 RECEPTOR ANTAGONISM Elan Pharmaceuticals Inc. (US) 2008-01-16 EP claimed
US-20070032475-A1 Novel compounds useful for bradykinin B1 receptor antagonism ELAN PHARMACEUTICALS, INC. 2007-02-08 US claimed
WO-2006113140-A2 NOVEL COMPOUNDS USEFUL FOR BRADYKININ B1 RECEPTOR ANTAGONISM ELAN PHARMACEUTICALS, INC. (US) 2006-10-26 WO claimed
US-20260132127-A1 NOVEL SPIRO COMPOUND MITSUBISHI TANABE PHARMA CORPORATION (JP) 2026-05-14 US disclosed
EP-4402138-B1 3-PHENOXYAZETIDIN-1-YL-HETEROARYL PYRROLIDINE DERIVATIVES AND THE USE THEREOF AS MEDICAMENT BOEHRINGER INGELHEIM INT (DE) 2025-08-27 EP disclosed
US-20250221988-A1 COMPOUNDS AND METHODS OF TREATING CANCERS CULLGEN (SHANGHAI), INC. (CN) 2025-07-10 US disclosed
WO-2025131957-A1 DIAZINONE COMPOUNDS FOR THE CONTROL OF INVERTEBRATE PESTS BASF SE (DE) 2025-06-26 WO disclosed
US-20250206722-A1 SMALL MOLECULE INHIBITORS OF TEA DOMAIN FAMILY MEMBERS THE SCRIPPS RESEARCH INSTITUTE 2025-06-26 US disclosed
EP-4504716-A1 COMPOUNDS AND METHODS OF TREATING CANCERS Cullgen (Shanghai), Inc. (CN) 2025-02-12 EP disclosed
CN-119403551-A Small molecule inhibitors of TEA domain family members 斯克里普斯研究学院 2025-02-07 CN disclosed
EP-4496570-A2 SMALL MOLECULE INHIBITORS OF TEA DOMAIN FAMILY MEMBERS The Scripps Research Institute (US) 2025-01-29 EP disclosed
CN-1781911-A Intermediate for producing novel pyrazine derivatives TOYAMA CHEMICAL CO LTD (JP) 2006-06-07 CN disclosed
CN-1239511-C Novel pyrazine derivative or salt thereof, and pharmaceutical composition containing the same TOYAMA CHEMICAL CO LTD (JP) 2006-02-01 CN disclosed
EP-1440075-B1 NOVEL 3BETA-AMINO AZABICYCLOOCTANE HETEROAROMATIC AMIDE DERIVATIVES, PREPARATION METHOD AND THERAPEUTIC USES THEREOF PF MEDICAMENT (FR) 2005-06-08 EP disclosed
EP-1440075-A1 NOVEL 3BETA-AMINO AZABICYCLOOCTANE HETEROAROMATIC AMIDE DERIVATIVES, PREPARATION METHOD AND THERAPEUTIC USES THEREOF PIERRE FABRE MEDICAMENT (FR) 2004-07-28 EP disclosed
CN-1418220-A Novel pyrazine derivative or salt thereof, pharmaceutical composition containing same, and intermediate for producing both TOYAMA CHEMICAL CO LTD (JP) 2003-05-14 CN disclosed
WO-2003037904-A1 NOVEL 3BETA-AMINO AZABICYCLOOCTANE HETEROAROMATIC AMIDE DERIVATIVES, PREPARATION METHOD AND THERAPEUTIC USES THEREOF PIERRE FABRE MEDICAMENT (FR) 2003-05-08 WO disclosed
CN-1300279-A Modulators of protein tyrosine phosphatases NOVO NORDISK AS (DK) 2001-06-20 CN disclosed
EP-0267740-A1 Naphthyridine and pyridopyrazine compounds and pharmaceutical usage thereof SCHERING CORPORATION (US) 1988-05-18 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 (4 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-20250206722-A1 SMALL MOLECULE INHIBITORS OF TEA DOMAIN FAMILY MEMBERS YAP1, TEAD1, TEAD2 SMN1; SMN2 2064/4885LMNA 2257/4885KDM4E 1214/4885
US-20250221988-A1 COMPOUNDS AND METHODS OF TREATING CANCERS GSPT1, GSS, G6PC1 SMN1; SMN2 2055/4885LMNA 3243/4885KDM4E 3268/4885
US-20260132127-A1 NOVEL SPIRO COMPOUND TRHR, NR3C2, THRB SMN1; SMN2 2423/4885LMNA 2025/4885KDM4E 4548/4885
US-20070032475-A1 Novel compounds useful for bradykinin B1 receptor antagonism BDKRB1, BDKRB2, NPBWR1 SMN1; SMN2 2731/4885LMNA 1762/4885KDM4E 4606/4885

“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.