SCHEMBL2137200

SCHEMBL2137200

N#Cc1cccc(Br)c1Cl

nearest known ligand 0.44

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
DYRK1A Q13627 2/20 0.44
CXCR1 P25024 1/20 0.43
CXCR2 P25025 1/20 0.43
LMNA P02545 1/20 0.41
TSHR P16473 1/20 0.38
TDP1 Q9NUW8 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
CA1 P00915 1/20 0.35
CA2 P00918 1/20 0.35
HTR2A P28223 1/20 0.35
HTR2C P28335 1/20 0.35
HTR2B P41595 1/20 0.35
LDHA P00338 2/20 0.34
LDHB P07195 2/20 0.34
AR P10275 2/20 0.33
MCL1 Q07820 1/20 0.33
TRPV4 Q9HBA0 1/20 0.33
HTT P42858 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
SCHEMBL31156147 1.00 DYRK1A (0.44) DYRK1ACXCR1CXCR2LMNATSHR
SCHEMBL3237062 0.83 TSHR (0.46) DYRK1ATSHRTDP1CA1CA2
SCHEMBL20899391 0.77 TRPV4 (0.42) DYRK1ACXCR1CXCR2TSHRL3MBTL1
SCHEMBL29284609 0.77 PDPK1 (0.31) TSHR
SCHEMBL8098752 0.77 JAK2 (0.31) CXCR1CXCR2LMNA
SCHEMBL16960784 0.77 PDPK1 (0.31)
SCHEMBL3386194 0.76 DYRK1A (0.47) DYRK1ACXCR1CXCR2LMNATSHR
SCHEMBL101977 0.76 DYRK1A (0.47) DYRK1ATSHRL3MBTL1CA1CA2
SCHEMBL31032883 0.76 DYRK1A (0.47) DYRK1ACXCR1CXCR2LMNATSHR
SCHEMBL27895311 0.76 DYRK1A (0.47) DYRK1ATSHRL3MBTL1CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12583840-B2 Method for the preparation of androgen receptor antagonists and intermediates thereof ORION CORPORATION (FI) 2026-03-24 US disclosed
US-12565476-B2 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric SHP2 inhibitors Revolution Medicines, Inc. (US) 2026-03-03 US disclosed
CN-120192300-A Method for preparing androgen receptor antagonist and intermediate thereof 奥赖恩公司 2025-06-24 CN disclosed
EP-4570313-A2 CYANOTRIAZOLE COMPOUNDS Otsuka Pharmaceutical Co., Ltd. (JP) 2025-06-18 EP disclosed
WO-2025106362-A1 RIPK1 INHIBITORS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2025-05-22 WO disclosed
CN-115605470-B Method for preparing androgen receptor antagonist and intermediate thereof 奥赖恩公司 2025-04-18 CN disclosed
US-12268687-B2 Compounds and uses thereof JANSSEN PHARMACEUTICA NV (BE) 2025-04-08 US disclosed
US-20250066357-A1 PROTEIN TYROSINE PHOSPHATASE INHIBITORS ARRAY BIOPHARMA INC. (US) 2025-02-27 US disclosed
US-20250034125-A1 COMPOUNDS AND USES THEREOF JANSSEN PHARMACEUTICA NV (BE) 2025-01-30 US disclosed
US-20250034124-A1 COMPOUNDS AND USES THEREOF JANSSEN PHARMACEUTICA NV (BE) 2025-01-30 US disclosed
CN-103180312-B Be used for the treatment of or prevent the heterogeneous ring compound of the disorder that the reduction because of the nerve conduction of thrombotonin, norepinephrine or Dopamine HCL causes OTSUKA PHARMACEUTICAL CO.,LTD. (JP) 2016-01-20 CN disclosed
CN-105143200-A Serine/threonine kinase inhibitors for the treatment of hyperproliferative|diseases ARRAY BIOPHARMA INC 2015-12-09 CN disclosed
WO-2015008872-A1 CYANOTRIAZOLE COMPOUNDS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2015-01-22 WO disclosed
CN-103180312-A Heterocyclic compounds for treating or preventing disorders caused by reduced neurotransmission of serotonin, norephnephrine or dopamine OTSUKA PHARMA CO LTD 2013-06-26 CN disclosed
EP-2445891-A1 5-MEMBERED HETEROARYL DERIVATIVES USED AS SPHINGOSINE 1-PHOSPHATE RECEPTOR AGONISTS Glaxo Group Limited (GB) 2012-05-02 EP disclosed
US-20120101134-A1 5-MEMBERED HETEROARYL DERIVATIVES USED AS SPHINGOSINE 1-PHOSPHATE RECEPTOR AGONISTS GLAXO GROUP LIMITED (GB) 2012-04-26 US disclosed
WO-2010148649-A1 5-MEMBERED HETEROARYL DERIVATIVES USED AS SPHINGOSINE 1-PHOSPHATE RECEPTOR AGONISTS GLAXO GROUP LIMITED (GB) 2010-12-29 WO disclosed
US-20080318929-A1 Pyrimidine Derivatives Useful as Inhibitors of Pkc-Theta BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2008-12-25 US disclosed
EP-1966163-A1 PYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF PKC-THETA Boehringer Ingelheim International GmbH (DE) 2008-09-10 EP disclosed
WO-2007076247-A1 PYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF PKC-THETA BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2007-07-05 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 (8 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-20250066357-A1 PROTEIN TYROSINE PHOSPHATASE INHIBITORS PPM1A, PPM1F, PPP5C DYRK1A 190/4885CXCR1 3379/4885CXCR2 2824/4885
US-20250034124-A1 COMPOUNDS AND USES THEREOF NLN, BDNF, NQO1 DYRK1A 3912/4885CXCR1 2788/4885CXCR2 1427/4885
US-12268687-B2 Compounds and uses thereof NLN, BDNF, NQO1 DYRK1A 3912/4885CXCR1 2788/4885CXCR2 1427/4885
US-12583840-B2 Method for the preparation of androgen receptor antagonists and intermediates thereof AR, FSHR, PKD1 DYRK1A 1979/4885CXCR1 1573/4885CXCR2 1982/4885
US-20080318929-A1 Pyrimidine Derivatives Useful as Inhibitors of Pkc-Theta PRKCQ, PRKCZ, PRKAR2B DYRK1A 801/4885CXCR1 1130/4885CXCR2 935/4885
US-20250034125-A1 COMPOUNDS AND USES THEREOF NLN, BDNF, NQO1 DYRK1A 3912/4885CXCR1 2788/4885CXCR2 1427/4885
US-20120101134-A1 5-MEMBERED HETEROARYL DERIVATIVES USED AS SPHINGOSINE 1-PHOSPHATE RECEPTOR AGONISTS S1PR1, S1PR5, S1PR3 DYRK1A 2598/4885CXCR1 717/4885CXCR2 789/4885
US-12565476-B2 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric SHP2 inhibitors PTPN5, PTPN6, PTPN2 DYRK1A 757/4885CXCR1 884/4885CXCR2 245/4885

“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.