SCHEMBL2588073

SCHEMBL2588073

Clc1cc2ncccc2c(Cl)n1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR4A2 P43354 2/20 0.50
KDM4E B2RXH2 2/20 0.46
MAPT P10636 2/20 0.46
METAP1 P53582 1/20 0.46
CCR1 P32246 2/20 0.43
CCR8 P51685 2/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
CYP3A4 P08684 2/20 0.42
ALDH1A1 P00352 5/20 0.42
CASP6 P55212 1/20 0.42
LMNA P02545 2/20 0.41
CDC7 O00311 2/20 0.41
DAPK3 O43293 2/20 0.41
PRKD3 O94806 2/20 0.41
MAP4K4 O95819 2/20 0.41
PAK4 O96013 2/20 0.41
PIM1 P11309 2/20 0.41
PRKACA P17612 2/20 0.41
CSNK1A1 P48729 2/20 0.41
CLK2 P49760 2/20 0.41

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
SCHEMBL16235635 0.81 NR4A2 (0.47) NR4A2KDM4EMAPTMETAP1CCR1
SCHEMBL31329846 0.81 NR4A2 (0.56) NR4A2KDM4EMAPTCCR1CCR8
Quinoline SCHEMBL28210108 0.80 ALDH1A1 (0.57) NR4A2KDM4EMAPTMETAP1CCR1
SCHEMBL30133446 0.77 SYK (0.55) NR4A2KDM4EMAPTCYP3A4LMNA
SCHEMBL26130603 0.77 SYK (0.55) NR4A2KDM4EMAPTCYP3A4LMNA
SCHEMBL30023109 0.75 LMNA (0.46) NR4A2KDM4EMAPTMETAP1L3MBTL1
SCHEMBL22201437 0.75 PRKCH (0.56) NR4A2KDM4EMAPTMETAP1ALDH1A1
SCHEMBL31170791 0.73 NR4A2 (0.52) NR4A2KDM4EMAPTMETAP1CCR1
SCHEMBL18529914 0.72 KDM4E (0.35) NR4A2KDM4EMETAP1CYP3A4LMNA
SCHEMBL523735 0.72 MAPT (0.58) NR4A2KDM4EMAPTMETAP1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12617791-B2 Triheterocyclic derivative, and pharmaceutical composition and application thereof Shanghai De Novo Pharmatech Co., Ltd. (CN) 2026-05-05 US disclosed
EP-4731216-A1 HETEROARYL-AMINE COMPOUNDS AND USE THEREOF AS HDAC6 INHIBITORS Augustine Therapeutics (BE) 2026-04-29 EP disclosed
US-12570671-B2 Substituted oxoisoindoline compounds for the treatment of cancer BRISTOL-MYERS SQUIBB COMPANY (US) 2026-03-10 US disclosed
EP-4126843-B1 SUBSTITUTED OXOISOINDOLINE COMPOUNDS FOR THE TREATMENT OF CANCER BRISTOL MYERS SQUIBB CO (US) 2026-02-11 EP disclosed
EP-4230628-B1 TRIHETEROCYCLIC DERIVATIVE, AND PHARMACEUTICAL COMPOSITION AND APPLICATION THEREOF SHANGHAI DE NOVO PHARMATECH CO LTD (CN) 2025-10-15 EP disclosed
US-20250263408-A1 SPLEEN TYROSINE KINASE INHIBITORS UNIQUEST PTY LTD (AU) 2025-08-21 US disclosed
US-12358931-B2 3-((1R,3s,5S)-3-((7-((5-methyl-1H-pyrazol-3-yl)amino)-1,6-naphthyridin-5-yl)amino)-8-azabicyclo[3.2.1]octan-8-yl) propanenitrile as a JAK kinase inhibitor THERAVANCE BIOPHARMA R&D IP, LLC (US) 2025-07-15 US disclosed
CN-116003441-B Heteroaromatic derivative regulator, preparation method and application thereof 江苏豪森药业集团有限公司 2025-06-10 CN disclosed
EP-4504724-A1 SPLEEN TYROSINE KINASE INHIBITORS Uniquest Pty Limited (AU) 2025-02-12 EP disclosed
CN-119325474-A Spleen tyrosine kinase inhibitors 尤尼奎斯特公司 2025-01-17 CN disclosed
US-8633319-B2 7-(1H-pyrazol-4-yl)-1,6-naphthyridine compounds as Syk inhibitors GLAXO GROUP LIMITED (GB) 2014-01-21 US disclosed
EP-2563789-A1 7-(1H-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS Glaxo Group Limited (GB) 2013-03-06 EP disclosed
CN-102947306-A 7-(1h-pyrazol-4-yl)-1,6-naphthyridine compounds as SYK inhibitors GLAXO GROUP LTD 2013-02-27 CN disclosed
US-20130040984-A1 7-(lH-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS GLAXO GROUP LIMITED (GB) 2013-02-14 US disclosed
US-20130040984-A1 7-(lH-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS GLAXO GROUP LIMITED (GB) 2013-02-14 US disclosed
US-20130040984-A1 7-(lH-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS GLAXO GROUP LIMITED (GB) 2013-02-14 US disclosed
WO-2011134971-A1 7-(1H-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS GLAXO GROUP LIMITED (GB) 2011-11-03 WO disclosed
WO-2011134971-A1 7-(1H-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS GLAXO GROUP LIMITED (GB) 2011-11-03 WO disclosed
US-7202249-B2 Antagonists of chemokine receptors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-04-10 US disclosed
US-20040048865-A1 Antagonists of chemokine receptors BRISTOL-MYERS SQUIBB COMPANY 2004-03-11 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 (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-12358931-B2 3-((1R,3s,5S)-3-((7-((5-methyl-1H-pyrazol-3-yl)amino)-1,6-naphthyridin-5-yl)amino)-8-azabicyclo[3.2.1]octan-8-yl) propanenitrile as a JAK kinase inhibitor JAK1, JAK3, JAK2 NR4A2 2491/4885KDM4E 272/4885MAPT 4182/4885
US-20130040984-A1 7-(lH-PYRAZOL-4-YL)-1,6-NAPHTHYRIDINE COMPOUNDS AS SYK INHIBITORS SYK, BTK, LYN NR4A2 1801/4885KDM4E 629/4885MAPT 3202/4885
US-12570671-B2 Substituted oxoisoindoline compounds for the treatment of cancer NR3C1, NR2C2, RIOX2 NR4A2 27/4885KDM4E 2872/4885MAPT 4488/4885
US-20250263408-A1 SPLEEN TYROSINE KINASE INHIBITORS LCK, BTK, SYK NR4A2 1712/4885KDM4E 644/4885MAPT 3900/4885
US-12617791-B2 Triheterocyclic derivative, and pharmaceutical composition and application thereof ATR, NR3C1, NR5A1 NR4A2 45/4885KDM4E 3222/4885MAPT 4596/4885
US-20040048865-A1 Antagonists of chemokine receptors CXCR2, CCR1, CXCR3 NR4A2 209/4885KDM4E 3036/4885MAPT 2194/4885

“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.