SCHEMBL2323949

SCHEMBL2323949

Clc1ccnc2ncccc12

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 7/20 0.48
MAPT P10636 5/20 0.48
LMNA P02545 5/20 0.48
HSP90AA1 P07900 4/20 0.48
METAP2 P50579 2/20 0.48
METAP1 P53582 2/20 0.48
BRD4 O60885 1/20 0.48
ALDH1A1 P00352 5/20 0.47
TDP1 Q9NUW8 5/20 0.47
MEN1 O00255 4/20 0.47
KMT2A Q03164 4/20 0.47
MMP14 P50281 3/20 0.47
CYP3A4 P08684 3/20 0.47
ALOX12 P18054 3/20 0.47
HTT P42858 3/20 0.47
SMN1; SMN2 Q16637 3/20 0.47
TP53 P04637 2/20 0.47
ALOX15 P16050 2/20 0.47
SLC6A2 P23975 2/20 0.47
OPRK1 P41145 2/20 0.47

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
SCHEMBL4359138 0.74 TRPV1 (0.43) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL22121720 0.74 TRPV1 (0.35) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL3764679 0.74 CCR1 (0.43) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL247512 0.74 L3MBTL1 (0.52) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL5239248 0.73 KDM4E (0.44) KDM4EMAPTLMNAHSP90AA1ALDH1A1
SCHEMBL2023814 0.73 AXL (0.39) KDM4EMAPTLMNAALDH1A1TDP1
SCHEMBL30831937 0.73 PDE4A (0.52) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL29416394 0.73 PDE4A (0.52) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL1065478 0.73 PDE4A (0.52) KDM4EMAPTLMNAHSP90AA1METAP2
SCHEMBL3151611 0.73 HSP90AA1 (0.45) KDM4EMAPTLMNAHSP90AA1METAP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104086543-A Method for preparing 4-chloro-1,8-naphthyridine Hunan huateng pharmaceutical co ltd 2014-10-08 CN claimed
CN-118369312-A Trirylene diimide and tetrarylene terephthalimide colorants 巴斯夫欧洲公司 2024-07-19 CN disclosed
CN-114249691-B Naphthalimide enhanced mercury ion fluorescent probe, preparation method and application 济南大学 2023-09-26 CN disclosed
CN-113166076-A Heterocyclic compounds for the treatment of epilepsy 大塚制药株式会社 2021-07-23 CN disclosed
EP-3133074-B1 7-AZAINDOLE DERIVATIVES MERCK PATENT GMBH (DE) 2020-12-09 EP disclosed
US-20200031811-A1 SUBSTITUTED MONO- AND POLYAZANAPHTHALENE DERIVATIVES AND THEIR USE BASILEA PHARM INT AG (CH) 2020-01-30 US disclosed
EP-2531500-B1 HETARYL-[1,8]NAPHTHYRIDINE DERIVATIVES MERCK PATENT GMBH (DE) 2018-01-24 EP disclosed
US-20180002321-A1 SUBSTITUTED MONO- AND POLYAZANAPHTHALENE DERIVATIVES AND THEIR USE Basilea Pharmaceutica International AG (CH) 2018-01-04 US disclosed
EP-3256217-A1 SUBSTITUTED MONO- AND POLYAZANAPHTHALENE DERIVATIVES AND THEIR USE Basilea Pharmaceutica International AG (CH) 2017-12-20 EP disclosed
CN-107226813-A A kind of method for preparing the bromo- 1,8- naphthridine of 4- 长沙深橙生物科技有限公司 2017-10-03 CN disclosed
WO-2005021546-A1 SUBSTITUTED NAPHTHYRIDINE DERIVATIVES AS INHIBITORS OF MACROPHAGE MIGRATION INHIBITORY FACTOR AND THEIR USE IN THE TREATMENT OF HUMAN DISEASES AVANIR PHARMACEUTICALS (US) 2005-03-10 WO disclosed
US-20040048865-A1 Antagonists of chemokine receptors BRISTOL-MYERS SQUIBB COMPANY 2004-03-11 US disclosed
EP-0060012-B1 4-HALO-1,8-NAPHTHYRIDINE DERIVATIVES USEFUL AS INTERMEDIATES AND PROCESSES FOR THEIR PREPARATION AMERICAN HOME PRODUCTS CORPORATION (US) 1984-08-29 EP disclosed
EP-0018735-B1 1,8-NAPHTHYRIDINE DERIVATIVES, THEIR PREPARATION, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AMERICAN HOME PRODUCTS CORPORATION (US) 1983-07-27 EP disclosed
US-4350817-A 4-Cl, Br or I-3-Carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives AMERICAN HOME PRODUCTS CORPORATION (US) 1982-09-21 US disclosed
EP-0060012-A1 4-Halo-1,8-naphthyridine derivatives useful as intermediates and processes for their preparation AMERICAN HOME PRODUCTS CORPORATION (US) 1982-09-15 EP disclosed
US-4347362-A HYPOTENSIVE AMERICAN HOME PRODUCTS CORPORATION (US) 1982-08-31 US disclosed
US-4324893-A 4-Amino-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives AMERICAN HOME PRODUCTS CORPORATION (US) 1982-04-13 US disclosed
EP-0018735-A1 1,8-Naphthyridine derivatives, their preparation, pharmaceutical compositions containing them AMERICAN HOME PRODUCTS CORPORATION (US) 1980-11-12 EP disclosed
WO-1980002287-A1 1,8-NAPHTHYRIDINE DERIVATIVES AMERICAN HOME PROD (US) 1980-10-30 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 (3 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-20180002321-A1 SUBSTITUTED MONO- AND POLYAZANAPHTHALENE DERIVATIVES AND THEIR USE CBR3, SCO2, CBR1 KDM4E 3811/4885MAPT 4837/4885LMNA 502/4885
US-20200031811-A1 SUBSTITUTED MONO- AND POLYAZANAPHTHALENE DERIVATIVES AND THEIR USE CBR3, SCO2, CBR1 KDM4E 3808/4885MAPT 4837/4885LMNA 500/4885
US-20040048865-A1 Antagonists of chemokine receptors CXCR2, CCR1, CXCR3 KDM4E 3036/4885MAPT 2194/4885LMNA 2737/4885

“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.