SCHEMBL455548

SCHEMBL455548

NNC(=S)Nc1ccc(F)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 7/20 1.00
MAPT P10636 3/20 0.64
KDM4E B2RXH2 2/20 0.64
GAA P10253 1/20 0.64
MEN1 O00255 3/20 0.62
KMT2A Q03164 3/20 0.62
LMNA P02545 1/20 0.62
MAPK1 P28482 1/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
NOX1 Q9Y5S8 1/20 0.60
POLB P06746 1/20 0.58
CA1 P00915 1/20 0.58
CA2 P00918 1/20 0.58
CA4 P22748 1/20 0.58
CA9 Q16790 1/20 0.58
MAOB P27338 2/20 0.56
MAOA P21397 1/20 0.56

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
Alcohol SCHEMBL28251608 0.92 IDO1 (0.85) IDO1MAPTKDM4EGAAMEN1
SCHEMBL455344 0.89 IDO1 (0.78) IDO1MAPTKDM4EGAAMEN1
SCHEMBL10099725 0.86 GAA (0.83) IDO1MAPTKDM4EGAAMEN1
SCHEMBL469849 0.82 NOX1 (0.84) IDO1MAPTKDM4EGAAMEN1
SCHEMBL7658710 0.81 MEN1 (0.68) IDO1MAPTKDM4EGAAMEN1
SCHEMBL1642748 0.80 IDO1 (0.67) IDO1MAPTKDM4EGAAMEN1
SCHEMBL455323 0.80 GAA (0.74) IDO1MAPTKDM4EGAAMEN1
SCHEMBL9036250 0.80 IDO1 (0.64) IDO1MAPTKDM4EGAAMEN1
SCHEMBL6302052 0.78 GAA (0.64) IDO1MAPTKDM4EGAAMEN1
SCHEMBL10710275 0.78 NOX1 (0.85) IDO1MAPTGAAMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102786464-B Phthiobuzonum derivative and its production and use BEIJING UNION PHARMACEUTICAL FACTORY (CN) 2016-05-11 CN claimed
CN-102786464-A Ftibamzone derivative and preparation method and application thereof BEIJING UNION PHARMACEUTICAL FACTORY 2012-11-21 CN claimed
CN-1990470-B Phthiobuzonum derivative, its manufacturing process, pharmaceutical combination and uses thereof BEIJING XIEHE PHARMACEUTICAL FACTORY 2011-04-20 CN claimed
CN-1671717-A Azole derivatives as antifungal agents RANBAXY LAB LTD (IN) 2005-09-21 CN claimed
US-12421207-B2 Pyrimidinedione-based compounds as AXL, c-MET, and Mer inhibitors and methods of use thereof CMG PHARMACEUTICAL CO., LTD. (KR) 2025-09-23 US disclosed
US-20250171426-A1 PYRIMIDINEDIONE-BASED COMPOUNDS AS AXL, C-MET, AND MER INHIBITORS AND METHODS OF USE THEREOF CMG PHARMACEUTICAL CO., LTD. (KR) 2025-05-29 US disclosed
WO-2025046420-A1 COMPOUND TARGETING EGR-1 AND USE THEREOF FOR TREATMENT OF ATOPIC DERMATITIS 주식회사 아제라메디 2025-03-06 WO disclosed
EP-4479397-A1 PYRIMIDINEDIONE-BASED COMPOUNDS AS AXL, C-MET, AND MER INHIBITORS AND METHODS OF USE THEREOF CMG Pharmaceutical Co., Ltd. (KR) 2024-12-25 EP disclosed
US-20240174666-A1 PYRAZOLO[3,4-b]PYRIDINE COMPOUNDS AS INHIBITORS OF TAM AND MET KINASES ARRAY BIOPHARMA INC. (US) 2024-05-30 US disclosed
CN-114634502-B 3-Aryl substituted thiazolidine-4-ketone-2-methylene hydrazono methylene-1H-indole derivative and preparation method thereof 复旦大学 2024-05-24 CN disclosed
EP-3843850-B1 PYRAZOLO[3,4-B]PYRIDINE COMPOUNDS AS INHIBITORS OF TAM AND MET KINASES ARRAY BIOPHARMA INC (US) 2023-11-15 EP disclosed
US-20230348423-A1 PYRIMIDINEDIONE-BASED COMPOUNDS AS AXL, C-MET, AND MER INHIBITORS AND METHODS OF USE THEREOF CMG PHARMACEUTICAL CO., LTD. (KR) 2023-11-02 US disclosed
EP-1697328-A1 PYRAZOLINOLS USED AS PESTICIDES Bayer CropScience Aktiengesellschaft (DE) 2006-09-06 EP disclosed
WO-2005092873-A2 THIADIAZOLES FOR TREATMENT OF CANCER OR NEUROLOGICAL DISEASE UNIWERSYTET MARII CURIE SKLODOWSKIEJ (PL) 2005-10-06 WO disclosed
CN-1671717-A Azole derivatives as antifungal agents RANBAXY LAB LTD (IN) 2005-09-21 CN disclosed
WO-2005058838-A1 PYRAZOLINOLS USED AS PESTICIDES BAYER CROPSCIENCE AKTIENGESELLSCHAFT (DE) 2005-06-30 WO disclosed
WO-2005051381-A1 Substituted urea-octatydroindols as antagonists of melanin concentrating hormone receptor 1 (MCH1R) BIOVITRUM AB (SE) 2005-06-09 WO disclosed
US-5571843-A Derivatives of indan-1,3-dione and indan-1,2,3-trione, methods of preparing them and therapeutic use thereof INNOTHERA (FR) 1996-11-05 US disclosed
EP-0566445-A1 Derivatives of indane 1,3-dione and indane-1,2,3-trione, processes for their preparation and their application in therapy INNOTHERA (FR) 1993-10-20 EP disclosed
WO-1993020045-A1 INDAN-1,3-DIONE AND INDAN-1,2,3-TRIONE DERIVATIVES, PROCESSES FOR THE PREPARATION OF SAME AND THEIR APPLICATION AS THERAPEUTIC AGENTS INNOTHERA (FR) 1993-10-14 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 (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-20250171426-A1 PYRIMIDINEDIONE-BASED COMPOUNDS AS AXL, C-MET, AND MER INHIBITORS AND METHODS OF USE THEREOF MERTK, AXL, RET IDO1 3652/4885MAPT 2509/4885KDM4E 1440/4885
US-20240174666-A1 PYRAZOLO[3,4-b]PYRIDINE COMPOUNDS AS INHIBITORS OF TAM AND MET KINASES RET, MERTK, MET IDO1 2711/4885MAPT 833/4885KDM4E 951/4885
US-12421207-B2 Pyrimidinedione-based compounds as AXL, c-MET, and Mer inhibitors and methods of use thereof MERTK, AXL, MET IDO1 3934/4885MAPT 2741/4885KDM4E 1703/4885
US-20230348423-A1 PYRIMIDINEDIONE-BASED COMPOUNDS AS AXL, C-MET, AND MER INHIBITORS AND METHODS OF USE THEREOF MERTK, AXL, MET IDO1 3934/4885MAPT 2741/4885KDM4E 1703/4885

“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.