SCHEMBL846091

SCHEMBL846091

N#Cc1ccnc(Cl)c1Cl

nearest known ligand 0.42

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LRRK2 Q5S007 4/20 0.42
ALDH1A1 P00352 2/20 0.39
NPSR1 Q6W5P4 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
KMT2A Q03164 2/20 0.36
MEN1 O00255 1/20 0.36
CSNK1A1 P48729 1/20 0.35
CLK4 Q9HAZ1 1/20 0.35
HTR2A P28223 1/20 0.35
HTR2C P28335 1/20 0.35
HTR2B P41595 1/20 0.35
CYP11B2 P19099 2/20 0.33
AR P10275 2/20 0.33
TRPV4 Q9HBA0 1/20 0.33
KHK P50053 1/20 0.33
KDM4E B2RXH2 1/20 0.33
KMO O15229 1/20 0.33

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
SCHEMBL30007698 1.00 LRRK2 (0.42) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL15659375 0.78 CYP11B2 (0.45) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL13074742 0.78 LRRK2 (0.40) LRRK2ALDH1A1NPSR1KMT2AMEN1
SCHEMBL28296292 0.78 LRRK2 (0.40) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL245839 0.78 CSNK1A1 (0.41) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL30211311 0.78 LRRK2 (0.40) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL1119092 0.78 FFAR1 (0.42) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL3287530 0.78 LRRK2 (0.40) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL31321212 0.78 CSNK1A1 (0.41) LRRK2ALDH1A1NPSR1TDP1KMT2A
SCHEMBL4103795 0.77 RXFP1 (0.34)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
CN-115461334-B Benzimidazole derivative, and preparation method and medical application thereof 深圳信立泰药业股份有限公司 2024-06-21 CN 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
WO-2023160672-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH LPA RECEPTOR ACTIVITY LHOTSE BIO , INC. (US) 2023-08-31 WO 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
US-20230203004-A1 RSV INHIBITING 3-SUBSTITUTED QUINOLINE AND CINNOLINE DERIVATIVES JANSSEN PHARMACEUTICA NV (BE) 2023-06-29 US disclosed
US-20230203004-A1 RSV INHIBITING 3-SUBSTITUTED QUINOLINE AND CINNOLINE DERIVATIVES JANSSEN PHARMACEUTICA NV (BE) 2023-06-29 US disclosed
EP-4139293-A1 RSV INHIBITING 3-SUBSTITUTED QUINOLINE AND CINNOLINE DERIVATIVES Janssen Sciences Ireland Unlimited Company (IE) 2023-03-01 EP disclosed
CN-115461336-A RSV inhibiting 3-substituted quinoline and cinnoline derivatives 爱尔兰詹森科学公司 2022-12-09 CN disclosed
WO-2006081072-A1 ANTAGONISTS OF THE MGLU RECEPTOR AND USES THEREOF ABBOTT LABORATORIES (US) 2006-08-03 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
EP-0822930-B1 PYRIDINE DERIVATIVE AND PESTICIDE KUMIAI CHEMICAL INDUSTRY CO (JP) 1999-07-28 EP disclosed
US-5789582-A HALOGENATING CYANOAROMATIC COMPOUNDS IN THE VAPOR PHASE NIPPON SHOKUBAI CO., LTD. (JP) 1998-08-04 US disclosed
US-5763463-A Pyridine compounds which are useful as pesticides KUMIAI CHEMICAL INDUSTRY CO., LTD. (JP) 1998-06-09 US disclosed
EP-0822930-A1 PYRIDINE DERIVATIVE AND PESTICIDE KumaiI Chemical Industry Co., Ltd. (JP) 1998-02-11 EP 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
WO-1996033975-A1 PYRIDINE DERIVATIVE AND PESTICIDE KUMIAI CHEMICAL INDUSTRY CO., LTD. (JP) 1996-10-31 WO 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 LRRK2 3194/4885ALDH1A1 39/4885NPSR1 3386/4885
US-20230203004-A1 RSV INHIBITING 3-SUBSTITUTED QUINOLINE AND CINNOLINE DERIVATIVES ACE2, SIRT7, ACE LRRK2 2611/4885ALDH1A1 1630/4885NPSR1 2407/4885
US-11713298-B2 Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino]acetic acid AASDHPPT, AADAT, ALDH7A1 LRRK2 3682/4885ALDH1A1 15/4885NPSR1 2928/4885
US-20240158354-A1 Process for Preparing 2-[[5-(3-Chlorophenyl)-3-Hydroxypyridine-2-Carbonyl]Amino]Acetic Acid AASDHPPT, AADAT, ALDH7A1 LRRK2 3682/4885ALDH1A1 15/4885NPSR1 2928/4885
US-12269802-B2 Process for preparing 2-[[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl] amino] acetic acid AASDHPPT, AADAT, ALDH7A1 LRRK2 3682/4885ALDH1A1 15/4885NPSR1 2928/4885

“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.