SCHEMBL3364776

SCHEMBL3364776

CCOP(=O)(OCC)c1ccc(Br)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.47
KMT2A Q03164 6/20 0.44
LMNA P02545 2/20 0.44
TDP1 Q9NUW8 1/20 0.43
MEN1 O00255 5/20 0.42
NPSR1 Q6W5P4 3/20 0.41
CA12 O43570 2/20 0.40
CA1 P00915 2/20 0.40
CA2 P00918 2/20 0.40
CA9 Q16790 2/20 0.40
CA4 P22748 1/20 0.40
CA5A P35218 1/20 0.40
CA7 P43166 1/20 0.40
CA5B Q9Y2D0 1/20 0.40
PTPN2 P17706 1/20 0.39
PTPN1 P18031 1/20 0.39
POLB P06746 1/20 0.39
HTR2A P28223 1/20 0.38
HTR2B P41595 1/20 0.38
ACHE P22303 1/20 0.38

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
SCHEMBL6829825 0.89 TDP1 (0.49) KMT2ATDP1MEN1NPSR1CA12
SCHEMBL9407115 0.83 TDP1 (0.45) KMT2ALMNATDP1MEN1NPSR1
SCHEMBL29449953 0.82 GAA (0.46) GAAKMT2ALMNAMEN1NPSR1
SCHEMBL107781 0.81 HPGD (0.48) GAAKMT2ALMNATDP1MEN1
SCHEMBL29449956 0.80 GAA (0.45) GAAKMT2ALMNAMEN1NPSR1
SCHEMBL2597681 0.80 POLB (0.44) GAAKMT2ATDP1MEN1NPSR1
SCHEMBL16868487 0.80 GAA (0.49) GAAKMT2ALMNAMEN1NPSR1
SCHEMBL23057071 0.79 TDP1 (0.43) KMT2ATDP1MEN1NPSR1CA12
SCHEMBL11140840 0.79 POLB (0.54) KMT2ATDP1MEN1NPSR1CA12
SCHEMBL6898817 0.79 TDP1 (0.43) KMT2ATDP1MEN1NPSR1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250326777-A1 COMPOUNDS, COMPOSITIONS AND METHODS THEREOF HEPAITECH BEIJING BIOPHARMA TECH CO LTD (CN) 2025-10-23 US disclosed
US-12421228-B2 Naphthyridine derivatives as PRC2 inhibitors Mirati Therapeutics, Inc. (US) 2025-09-23 US disclosed
US-20250282787-A1 SUBSTITUTED IMIDAZO[1,2-c]PYRIMIDINES AS PRC2 INHIBITORS Mirati Therapeutics, Inc. 2025-09-11 US disclosed
US-12371435-B2 Substituted imidazo[1,2-c]pyrimidines as PRC2 inhibitors Mirati Therapeutics, Inc. (US) 2025-07-29 US disclosed
US-20250179082-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER Mirati Therapeutics, Inc. 2025-06-05 US disclosed
EP-4097099-B9 HETEROCYCLIC GLP-1 AGONISTS GASHERBRUM BIO INC (US) 2025-04-30 EP disclosed
US-12252493-B2 Imidazo[1,2-c]pyrimidine derivatives as PRC2 inhibitors for treating cancer Mirati Therapeutics, Inc. (US) 2025-03-18 US disclosed
WO-2025043191-A1 PRC2 INHIBITORS FOR USE IN TREATING SICKLE CELL DISEASE ORIC PHARMACEUTICALS, INC. (US) 2025-02-27 WO disclosed
US-20240398811-A1 PRC2 INHIBITORS FOR USE IN TREATING BLOOD DISORDERS ORIC PHARMACEUTICALS, INC. 2024-12-05 US disclosed
US-20240366639-A1 HETEROCYCLIC GLP-1 AGONISTS GASHERBRUM BIO INC (US) 2024-11-07 US disclosed
CN-1136198-C Novel benzyl pyrimidines ��������ҩ�ɷ����޹�˾ 2004-01-28 CN disclosed
WO-2003090690-A2 CELLULAR ACCUMULATION OF PHOSPHONATE ANALOGS OF HIV PROTEASE INHIBITOR COMPOUNDS AND THE COMPOUNDS AS SUCH GILEAD SCIENCES, INC. (US) 2003-11-06 WO disclosed
US-6353083-B1 CONJUGATED COPOLYMER COMPRISING UNITS DERIVED FROM 9-SUBSTITUTED FLUORENE MONOMERS AND/OR 9,9-DISUBSTITUTED FLUORENE MONOMERS AND TWO DISTINCT RESIDUAL MONOMERIC UNITS THAT HAVE HOLE TRANSPORTING PROPERTIES THE DOW CHEMICAL COMPANY 2002-03-05 US disclosed
CN-1337987-A Fluorene copolymers and devices made therefrom DOW CHEMICAL CO (US) 2002-02-27 CN disclosed
EP-1155096-A1 FLUORENE COPOLYMERS AND DEVICES MADE THEREFROM THE DOW CHEMICAL COMPANY (US) 2001-11-21 EP disclosed
WO-2000046321-A1 FLUORENE COPOLYMERS AND DEVICES MADE THEREFROM THE DOW CHEMICAL COMPANY (US) 2000-08-10 WO disclosed
CN-1166831-A Novel benzyl pyrimidines HOFFMANN LA ROCHE (CH) 1997-12-03 CN disclosed
EP-0303186-B1 Aryl phosphorus derivatives, their preparation and their use BASF AG (DE) 1993-11-10 EP disclosed
EP-0303186-A2 Aryl phosphorus derivatives, their preparation and their use BASF Aktiengesellschaft (DE) 1989-02-15 EP disclosed
US-4069247-A Preparation of phosphonic and/or phosphinic acids HOECHST AKTIENGESELLSCHAFT (DT) 1978-01-17 US 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 (8 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-20240366639-A1 HETEROCYCLIC GLP-1 AGONISTS GLP1R, GIPR, GCGR GAA 1076/4885KMT2A 4022/4885LMNA 3168/4885
US-12371435-B2 Substituted imidazo[1,2-c]pyrimidines as PRC2 inhibitors EZH2, BMI1, SUZ12 GAA 3443/4885KMT2A 8/4885LMNA 3643/4885
US-12252493-B2 Imidazo[1,2-c]pyrimidine derivatives as PRC2 inhibitors for treating cancer BMI1, EZH2, SUZ12 GAA 2893/4885KMT2A 47/4885LMNA 3710/4885
US-20250282787-A1 SUBSTITUTED IMIDAZO[1,2-c]PYRIMIDINES AS PRC2 INHIBITORS EZH2, BMI1, SUZ12 GAA 3417/4885KMT2A 28/4885LMNA 3805/4885
US-20250326777-A1 COMPOUNDS, COMPOSITIONS AND METHODS THEREOF MRGPRX4, MRGPRX1, MRGPRX2 GAA 169/4885KMT2A 2511/4885LMNA 1156/4885
US-20250179082-A1 IMIDAZO[1,2-C]PYRIMIDINE DERIVATIVES AS PRC2 INHIBITORS FOR TREATING CANCER BMI1, EZH2, SUZ12 GAA 2893/4885KMT2A 47/4885LMNA 3710/4885
US-20240398811-A1 PRC2 INHIBITORS FOR USE IN TREATING BLOOD DISORDERS EZH2, BMI1, EZH1 GAA 1232/4885KMT2A 10/4885LMNA 3326/4885
US-12421228-B2 Naphthyridine derivatives as PRC2 inhibitors BMI1, EZH2, SUZ12 GAA 2256/4885KMT2A 51/4885LMNA 3312/4885

“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.