SCHEMBL364531

SCHEMBL364531

Oc1cc(Cl)cc2cccnc12

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 14/20 0.57
L3MBTL1 Q9Y468 9/20 0.57
NPC1 O15118 7/20 0.57
RAB9A P51151 6/20 0.57
COMT P21964 2/20 0.57
METAP2 P50579 2/20 0.57
METAP1 P53582 2/20 0.57
MMP2 P08253 1/20 0.57
CHRM1 P11229 1/20 0.57
TSHR P16473 1/20 0.57
ADRA1A P35348 1/20 0.57
HDAC8 Q9BY41 1/20 0.57
MAPT P10636 2/20 0.54
PKM P14618 1/20 0.54
NFKB1 P19838 1/20 0.54
HTT P42858 1/20 0.54
CASP6 P55212 1/20 0.54
NFKB2 Q00653 1/20 0.54
RELA Q04206 1/20 0.54
SMN1; SMN2 Q16637 1/20 0.54

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
SCHEMBL11808148 0.80 COMT (0.61) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL20176005 0.78 KDM4E (0.59) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL3711196 0.78 KDM4E (0.59) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL20180977 0.77 KDM4E (0.57) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL28982408 0.77 KDM4E (0.57) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL6526164 0.77 KDM4E (0.62) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL28836360 0.77 KDM4E (0.57) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL20176000 0.77 KDM4E (0.57) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL3347624 0.77 KDM4E (0.57) KDM4EL3MBTL1NPC1RAB9ACOMT
SCHEMBL687398 0.77 PSMD14 (0.62) KDM4EL3MBTL1NPC1RAB9ACOMT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12503440-B2 Nitroxoline derivative, preparation method therefor, and use thereof Jiangsu Yahong Meditech Co. (CN) 2025-12-23 US disclosed
US-20230295094-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF ASIERIS PHARMACEUTICALS (SHANGHAI) CO., LTD. (CN) 2023-09-21 US disclosed
US-20230295094-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF ASIERIS PHARMACEUTICALS (SHANGHAI) CO., LTD. (CN) 2023-09-21 US disclosed
US-20230295094-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF ASIERIS PHARMACEUTICALS (SHANGHAI) CO., LTD. (CN) 2023-09-21 US disclosed
EP-4194441-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF Jiangsu Yahong Meditech Co., Ltd. (CN) 2023-06-14 EP disclosed
EP-4194441-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF Jiangsu Yahong Meditech Co., Ltd. (CN) 2023-06-14 EP disclosed
CN-115867540-A Nitroxoline derivatives, preparation method and application thereof 江苏亚虹医药科技股份有限公司 2023-03-28 CN disclosed
WO-2022028321-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF 江苏亚虹医药科技股份有限公司 2022-02-10 WO disclosed
CN-111960998-A Nitroxoline derivatives, preparation method and application thereof 江苏亚虹医药科技有限公司 2020-11-20 CN disclosed
US-9028562-B2 Dye composition using a 2-hydroxynaphthalene, (acylamino)phenol or quinoline coupler in a fatty-substance-rich medium, dyeing process and device therefor L'OREAL (FR) 2015-05-12 US disclosed
US-20140041133-A1 DYE COMPOSITION USING A 2-HYDROXYNAPHTHALENE, (ACYLAMINO)PHENOL OR QUINOLINE COUPLER IN A FATTY-SUBSTANCE-RICH MEDIUM, DYEING PROCESS AND DEVICE THEREFOR L'OREAL (FR) 2014-02-13 US disclosed
US-8592629-B2 Sulfonamide derivatives as Nav 1.7 inhibitors PFIZER LIMITED (GB) 2013-11-26 US disclosed
EP-2593432-A1 N-SULFONYLBENZAMIDE DERIVATIVES USEFUL AS VOLTAGE GATED SODIUM CHANNEL INHIBITORS Pfizer Limited (GB) 2013-05-22 EP disclosed
WO-2012007861-A1 N-SULFONYLBENZAMIDE DERIVATIVES USEFUL AS VOLTAGE GATED SODIUM CHANNEL INHIBITORS PFIZER LIMITED (GB) 2012-01-19 WO disclosed
WO-2012007861-A1 N-SULFONYLBENZAMIDE DERIVATIVES USEFUL AS VOLTAGE GATED SODIUM CHANNEL INHIBITORS PFIZER LIMITED (GB) 2012-01-19 WO disclosed
US-20120010183-A1 Chemical Compounds PFIZER LIMITED (GB) 2012-01-12 US disclosed
US-20120010183-A1 Chemical Compounds PFIZER LIMITED (GB) 2012-01-12 US disclosed
US-20120010183-A1 Chemical Compounds PFIZER LIMITED (GB) 2012-01-12 US disclosed
US-5489501-A MIXTURES OF TWO COORDINATION COMPOUNDS WHICH REACT TO FORM NEW COORDINATION COMPOUND WHILE CAUSING VISIBLE COLOR CHANGES RICOH COMPANY, LTD. (JP) 1996-02-06 US disclosed
EP-0153908-A1 Process for the preparation of pyridine-2,3-dicarboxylic acid CIBA-GEIGY AG (CH) 1985-09-04 EP 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 (4 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-20140041133-A1 DYE COMPOSITION USING A 2-HYDROXYNAPHTHALENE, (ACYLAMINO)PHENOL OR QUINOLINE COUPLER IN A FATTY-SUBSTANCE-RICH MEDIUM, DYEING PROCESS AND DEVICE THEREFOR HADHB, HADH, FABP4 KDM4E 1743/4885L3MBTL1 4792/4885NPC1 3508/4885
US-12503440-B2 Nitroxoline derivative, preparation method therefor, and use thereof NOS1, NQO1, NOS2 KDM4E 3548/4885L3MBTL1 4005/4885NPC1 384/4885
US-20120010183-A1 Chemical Compounds SCN1A, SCN1B, SCN7A KDM4E 3227/4885L3MBTL1 4470/4885NPC1 1272/4885
US-20230295094-A1 NITROXOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND USE THEREOF NOS1, NQO1, NOS2 KDM4E 3548/4885L3MBTL1 4005/4885NPC1 384/4885

“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.