SCHEMBL1007112

SCHEMBL1007112

N#Cc1nccc(Cl)c1Cl

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.42
KDM4E B2RXH2 3/20 0.42
POLB P06746 1/20 0.42
LRRK2 Q5S007 2/20 0.42
KMO O15229 2/20 0.36
ALOX15 P16050 1/20 0.34
ERBB2 P04626 1/20 0.32
AXL P30530 1/20 0.32
PRKCI P41743 1/20 0.32
BCAT1 P54687 1/20 0.32
CSNK1A1 P48729 1/20 0.31
CLK4 Q9HAZ1 1/20 0.31
LMNA P02545 2/20 0.31
CYP11B1 P15538 1/20 0.31
MAPT P10636 1/20 0.31
PKM P14618 1/20 0.31
MAPK1 P28482 1/20 0.31
RAB9A P51151 1/20 0.31
CACNA1B Q00975 1/20 0.31
APBA1 Q02410 1/20 0.31

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
SCHEMBL30692909 1.00 ALDH1A1 (0.42) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL19798188 0.78 KDM4E (0.40) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL31727717 0.78 KDM4E (0.40) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL29672973 0.78 KDM4E (0.40) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL11041531 0.78 KDM4E (0.36) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL23500465 0.78 ALDH1A1 (0.36) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL3360364 0.78 KDM4E (0.36) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL14783084 0.78 KDM4E (0.40) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL20899365 0.78 KDM4E (0.36) ALDH1A1KDM4EPOLBLRRK2KMO
SCHEMBL26331236 0.78 CSNK1A1 (0.37) ALDH1A1KDM4EPOLBLRRK2KMO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12441724-B2 Inhibitors of plasma kallikrein and uses thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2025-10-14 US disclosed
US-20250243164-A1 PROCESS FOR PREPARING 2-[[5-(3-CHLOROPHENYL)-3-HYDROXYPYRIDINE-2-CARBONYL]AMINO]ACETIC ACID AKEBIA THERAPEUTICS, INC. 2025-07-31 US disclosed
EP-3848370-B1 TYK2 INHIBITORS AND USES THEREOF TAKEDA PHARMACEUTICALS CO (JP) 2025-05-07 EP disclosed
US-12269802-B2 Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl] amino] acetic acid AKEBIA THERAPEUTICS, INC. (US) 2025-04-08 US disclosed
EP-3630749-B9 2-QUINOLONE DERIVED INHIBITORS OF BCL6 CANCER RESEARCH TECH LTD (GB) 2024-05-29 EP disclosed
EP-4371562-A2 2-QUINOLONE DERIVED INHIBITORS OF BCL6 Cancer Research Technology Limited (GB) 2024-05-22 EP disclosed
US-20240158354-A1 Process for Preparing 2-[[5-(3-Chlorophenyl)-3-Hydroxypyridine-2-Carbonyl]Amino]Acetic Acid KREOS CAPITAL VII (UK) LIMITED (GB) 2024-05-16 US disclosed
CN-117417923-A Nitrilase mutant and application thereof 浙江工业大学 2024-01-19 CN disclosed
EP-3630749-B1 2-QUINOLONE DERIVED INHIBITORS OF BCL6 CANCER RESEARCH TECH LTD (GB) 2024-01-10 EP disclosed
US-11713298-B2 Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid AKEBIA THERAPEUTICS, INC. (US) 2023-08-01 US disclosed
WO-2013033981-A1 2,7-NAPHTHYRIDINE DERIVATIVE, PREPARATION METHOD THEREFOR AND USE THEREOF 江苏先声药物研究有限公司 (CN) 2013-03-14 WO disclosed
CN-102712636-A Compounds and compositions as TLR activity modulators IRM LLC 2012-10-03 CN disclosed
WO-2012103044-A1 PROCESS FOR THE PREPARATION OF 4-AMINO-3-CHLORO-5-FLUORO-6-(SUBSTITUTED)PICOLINATES DOW AGROSCIENCES LLC (US) 2012-08-02 WO disclosed
EP-2268618-A1 COMPOUNDS AND COMPOSITIONS AS TLR ACTIVITY MODULATORS IRM LLC (BM) 2011-01-05 EP disclosed
WO-2009111337-A1 COMPOUNDS AND COMPOSITIONS AS TLR ACTIVITY MODULATORS IRM LLC (BM) 2009-09-11 WO disclosed
EP-0795541-B1 Method for production of nuclear halogenated aromatic compound possessing cyano groups NIPPON CATALYTIC CHEM IND (JP) 2001-11-14 EP disclosed
US-6034264-A VAPOR PHASE REACTION; USING ACTIVATED CARBON AS CATALYST NIPPON SHOKUBAI CO., LTD. (JP) 2000-03-07 US disclosed
US-5789582-A HALOGENATING CYANOAROMATIC COMPOUNDS IN THE VAPOR PHASE NIPPON SHOKUBAI CO., LTD. (JP) 1998-08-04 US disclosed
EP-0795541-A1 Method for production of nuclear halogenated aromatic compound possessing cyano groups NIPPON SHOKUBAI CO., LTD. (JP) 1997-09-17 EP disclosed
US-4766219-A Preparation of 2-cyano-6-chloropyridine compounds THE DOW CHEMICAL COMPANY (US) 1988-08-23 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 (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-20250243164-A1 PROCESS FOR PREPARING 2-[[5-(3-CHLOROPHENYL)-3-HYDROXYPYRIDINE-2-CARBONYL]AMINO]ACETIC ACID AASDHPPT, AADAT, HPD ALDH1A1 39/4885KDM4E 1427/4885POLB 2556/4885
US-12441724-B2 Inhibitors of plasma kallikrein and uses thereof KLKB1, KLK1, KLK5 ALDH1A1 3157/4885KDM4E 738/4885POLB 4589/4885
US-11713298-B2 Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid AASDHPPT, AADAT, ALDH7A1 ALDH1A1 15/4885KDM4E 1837/4885POLB 2135/4885
US-20240158354-A1 Process for Preparing 2-[[5-(3-Chlorophenyl)-3-Hydroxypyridine-2-Carbonyl]Amino]Acetic Acid AASDHPPT, AADAT, ALDH7A1 ALDH1A1 15/4885KDM4E 1837/4885POLB 2135/4885
US-12269802-B2 Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl] amino] acetic acid AASDHPPT, AADAT, ALDH7A1 ALDH1A1 15/4885KDM4E 1837/4885POLB 2135/4885

“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.