SCHEMBL237460

SCHEMBL237460

N=C(N)c1ccc2oc(CCc3cc4cc(C(=N)N)ccc4o3)cc2c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ F2 P00734 6/20 1.00
▸ F10 P00742 4/20 1.00
▸ PRMT1 Q99873 6/20 0.59
▸ TPSAB1 Q15661 1/20 0.49
▸ TPSD1 Q9BZJ3 1/20 0.49
▸ TPSG1 Q9NRR2 1/20 0.49

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
Hydrochloric Acid SCHEMBL5028046 0.98 F2 (0.97) F2F10PRMT1TPSAB1TPSD1
SCHEMBL5030493 0.93 F2 (0.88) F2F10PRMT1TPSAB1TPSD1
SCHEMBL5028071 0.93 F2 (0.88) F2F10PRMT1
Hydrochloric Acid SCHEMBL5034703 0.92 F2 (0.85) F2F10PRMT1
Hydrochloric Acid SCHEMBL5034833 0.92 F2 (0.85) F2F10PRMT1
SCHEMBL5032861 0.92 F2 (0.85) F2F10PRMT1TPSAB1TPSD1
SCHEMBL7979967 0.92 F2 (0.85) F2F10PRMT1TPSAB1TPSD1
Hydrochloric Acid SCHEMBL5031493 0.91 F2 (0.82) F2F10PRMT1TPSAB1TPSD1
SCHEMBL5034730 0.90 F2 (0.81) F2F10PRMT1TPSAB1TPSD1
Hydrochloric Acid SCHEMBL5028092 0.88 F2 (0.79) F2F10PRMT1TPSAB1TPSD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1689732-A4 CATIONIC SUBSTITUTED BENZOFURANS AS ANTIMICROBIAL AGENTS UNIV NORTH CAROLINA (US) 2008-10-22 — — EP claimed
US-20080114047-A1 Cationic substituted benzofurans as antimicrobial agents NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2008-05-15 — — US claimed
EP-1689732-A2 CATIONIC SUBSTITUTED BENZOFURANS AS ANTIMICROBIAL AGENTS The University of North Carolina at Chapel Hill (US) 2006-08-16 — — EP claimed
US-20050197378-A1 Cationic substituted benzofurans as antimicrobial agents TIDWELL RICHARD R (US) 2005-09-08 — — US claimed
WO-2005055935-A2 CATIONIC SUBSTITUTED BENZOFURANS AS ANTIMICROBIAL AGENTS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2005-06-23 — — WO claimed
US-5990079-A INDWELLING INTRAVASCULAR DEVICE COMPRISING FACTOR XA AND BIOLOGICALLY ACTIVE PEPTIDE FRAGMENTS THEREOF WHICH HAVE BEEN TRANSIENTLY INACTIVATED; THE FACTOR XA GENERATES AN ACTIVE FORM IN THE PRESENCE OF SERUM; INCREASED HALF-LIFE IN BLOOD COR THERAPEUTICS INC. (US) 1999-11-23 — — US claimed
US-5968897-A CARDIOVASCULAR DISORDERS AND BLOOD FACTORS COR THERAPEUTICS, INC. (US) 1999-10-19 — — US claimed
EP-1945209-B1 BROAD SPECTRUM ANTIBACTERIAL COMPOUNDS US GOV AS REPRESENTED BY THE SECRETARY OF THE UNITED STATES ARMY AND THE U S ARMY MEDICAL RESEARCH (US) 2018-05-30 — — EP disclosed
US-20170182049-A1 NOVEL THERAPEUTICS FOR BRAIN CANCER THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2017-06-29 — — US disclosed
US-20170182049-A1 NOVEL THERAPEUTICS FOR BRAIN CANCER THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2017-06-29 — — US disclosed
US-8389261-B2 Method of isolation and purification of trypsin from pronase protease and use thereof BAXTER HEALTHCARE S.A. (CH) 2013-03-05 — — US disclosed
US-20120003691-A1 METHOD OF ISOLATION AND PURIFICATION OF TRYPSIN FROM PRONASE PROTEASE AND USE THEREOF BAXTER HEALTHCARE S.A. (CH) 2012-01-05 — — US disclosed
EP-1456228-B1 METHOD OF ISOLATION AND PURIFICATION OF TRYPSIN FROM PRONASE AND USE THEREOF BAXTER HEALTHCARE SA (CH) 2011-05-04 — — EP disclosed
US-5602233-A ACTIVATION AND DEACTIVATION COR THERAPEUTICS, INC. (US) 1997-02-11 — — US disclosed
US-5589572-A Process for production of inhibited forms of activated blood factors COR THERAPEUTICS, INC. (US) 1996-12-31 — — US disclosed
US-5589571-A Process for production of inhibited forms of activated blood factors COR THERAPEUTICS, INC. (US) 1996-12-31 — — US disclosed
US-5583107-A ACYLATED BLOOD FACTOR XA AS TREATMENT FOR HEMOPHILIA COR THERAPEUTICS, INC. (US) 1996-12-10 — — US disclosed
US-5576343-A ANTICOAGULANTS; BLOOD-COAGULATION FACTOR X INHIBITORS DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1996-11-19 — — US disclosed
EP-0540051-B1 Aromatic amidine derivatives and salts thereof DAIICHI SEIYAKU CO (JP) 1996-04-03 — — EP disclosed
EP-0540051-A1 Aromatic amidine derivatives and salts thereof DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1993-05-05 — — 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-20080114047-A1 Cationic substituted benzofurans as antimicrobial agents BET1, ARG2, BRDT F2 2791/4885F10 2781/4885PRMT1 1394/4885
US-20050197378-A1 Cationic substituted benzofurans as antimicrobial agents BET1, ARG2, BRDT F2 2791/4885F10 2781/4885PRMT1 1394/4885
US-20170182049-A1 NOVEL THERAPEUTICS FOR BRAIN CANCER ING2, GMFG, PLP2 F2 4794/4885F10 3374/4885PRMT1 2298/4885
US-20120003691-A1 METHOD OF ISOLATION AND PURIFICATION OF TRYPSIN FROM PRONASE PROTEASE AND USE THEREOF PRSS3, RNPEP, NPEPPS F2 1298/4885F10 2072/4885PRMT1 3339/4885

“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.

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