SCHEMBL505159

SCHEMBL505159

N#Cc1cc(Cl)cc(Br)c1

nearest known ligand 0.43

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.43
TTR P02766 1/20 0.43
ALB P02768 1/20 0.43
KMT2A Q03164 1/20 0.43
GRM5 P41594 8/20 0.37
VCAM1 P19320 1/20 0.36
MAOA P21397 2/20 0.34
MAOB P27338 2/20 0.34
CYP1A2 P05177 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
SCHEMBL30020984 1.00 MEN1 (0.43) MEN1TTRALBKMT2AGRM5
SCHEMBL504640 0.82 TTR (0.52) MEN1TTRALBKMT2AVCAM1
SCHEMBL633226 0.82 TSHR (0.50) MEN1TTRALBKMT2AGRM5
SCHEMBL200313 0.82 TTR (0.52) MEN1TTRALBKMT2AVCAM1
SCHEMBL5852713 0.82 VCAM1 (0.43) MEN1TTRALBKMT2AGRM5
SCHEMBL2945314 0.76 TSHR (0.32)
SCHEMBL21313408 0.76 MMP3 (0.44) GRM5MAOAMAOB
SCHEMBL16950941 0.73 TTR (0.44) MEN1TTRALBKMT2AVCAM1
SCHEMBL114694 0.73
SCHEMBL151031 0.73

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12637428-B2 Isoquinoline derivatives as SIK2 inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2026-05-26 US disclosed
EP-4294800-B1 APOL1 INHIBITORS AND METHODS OF USE MAZE THERAPEUTICS INC (US) 2026-05-06 EP disclosed
US-20260085063-A1 BENZAMIDE COMPOUNDS AND METHODS OF USE THEREOF UNIV RUTGERS (US) 2026-03-26 US disclosed
US-20260055083-A1 APOL1 INHIBITORS AND METHODS OF USE MAZE THERAPEUTICS INC (US) 2026-02-26 US disclosed
US-12558341-B2 Oral complement factor D inhibitors BIOCRYST PHARMACEUTICALS, INC. (US) 2026-02-24 US disclosed
US-12552772-B2 2-pyrazole anilines and related analogs for inhibiting YAP/TAZ-TEAD SPRINGWORKS THERAPEUTICS, INC. (US) 2026-02-17 US disclosed
US-20260027113-A1 PHTHALAZINONE BASED MODULATORS FOR THE TREATMENT OF DISEASE SOLEY THERAPEUTICS INC (US) 2026-01-29 US disclosed
US-12465603-B2 Phthalazinone based modulators for the treatment of disease SOLEY THERAPEUTICS, INC. (US) 2025-11-11 US disclosed
EP-4619387-A1 PHTHALAZINONE BASED MODULATORS FOR THE TREATMENT OF DISEASE Soley Therapeutics, Inc. (US) 2025-09-24 EP disclosed
EP-4594308-A1 N-ACRYLOYLMORPHOLINE DERIVATIVES AS KEAP1 MODULATORS AND USES THEREOF Vividion Therapeutics, Inc. (US) 2025-08-06 EP disclosed
WO-2010021680-A2 INHIBITORS OF BETA-SECRETASE VITAE PHARMACEUTICALS, INC. (US) 2010-02-25 WO disclosed
WO-2010021680-A2 INHIBITORS OF BETA-SECRETASE VITAE PHARMACEUTICALS, INC. (US) 2010-02-25 WO disclosed
WO-2009149135-A1 BIS (HETERO ) ARYL SUBSTITUTED ISOXAZOLES FOR USE AS NEURONAL NICOTINIC RECEPTOR MODULATORS ABBOTT LABORATORIES (US) 2009-12-10 WO disclosed
US-20090306096-A1 Novel Isoxazoles and Methods of Use Thereof ABBOTT LABORATORIES (US) 2009-12-10 US disclosed
US-20090270393-A1 Iminopyridine Derivatives and Use Thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-10-29 US disclosed
WO-2009131245-A1 IMINOPYRIDINE DERIVATIVES AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-10-29 WO disclosed
US-7381856-B2 Carbon-carbon cross coupling catalyzed by transition metals on solid supports WYETH (US) 2008-06-03 US disclosed
EP-1687282-A2 CARBON-CARBON CROSS COUPLING CATALYZED BY TRANSITION METALS ON SOLID SUPPORTS Wyeth (US) 2006-08-09 EP disclosed
US-20050137438-A1 Carbon-carbon cross coupling catalyzed by transition metals on solid supports WYETH (US) 2005-06-23 US disclosed
WO-2005051869-A2 CARBON-CARBON CROSS COUPLING CATALYZED BY TRANSITION METALS ON SOLID SUPPORTS WYETH (US) 2005-06-09 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 (10 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-12465603-B2 Phthalazinone based modulators for the treatment of disease MKI67, BCL2, CCAR2 MEN1 1555/4885TTR 3982/4885ALB 4493/4885
US-20050137438-A1 Carbon-carbon cross coupling catalyzed by transition metals on solid supports SMARCC2, SMARCC1, SCO2 MEN1 783/4885TTR 2841/4885ALB 2556/4885
US-20260027113-A1 PHTHALAZINONE BASED MODULATORS FOR THE TREATMENT OF DISEASE NCOR1, NOP56, NCOR2 MEN1 2848/4885TTR 3135/4885ALB 3875/4885
US-20090306096-A1 Novel Isoxazoles and Methods of Use Thereof XDH, PRDX5, CYP4X1 MEN1 4307/4885TTR 2799/4885ALB 3765/4885
US-12637428-B2 Isoquinoline derivatives as SIK2 inhibitors SIK2, SIK1, SIK3 MEN1 2304/4885TTR 3587/4885ALB 4328/4885
US-12552772-B2 2-pyrazole anilines and related analogs for inhibiting YAP/TAZ-TEAD YAP1, TEAD3, TEAD2 MEN1 3883/4885TTR 2662/4885ALB 4174/4885
US-12558341-B2 Oral complement factor D inhibitors CFD, CFH, CFB MEN1 1819/4885TTR 171/4885ALB 357/4885
US-20260055083-A1 APOL1 INHIBITORS AND METHODS OF USE APOL1, LDLR, APOB MEN1 2120/4885TTR 122/4885ALB 1330/4885
US-20260085063-A1 BENZAMIDE COMPOUNDS AND METHODS OF USE THEREOF ACE2, CTRL, CTSL MEN1 4054/4885TTR 1440/4885ALB 895/4885
US-20090270393-A1 Iminopyridine Derivatives and Use Thereof ADRA1D, ADRB1, ADRB2 MEN1 818/4885TTR 4056/4885ALB 3991/4885

“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.