SCHEMBL333582

SCHEMBL333582

COc1ccc(CBr)cc1Br

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.56
SMN1; SMN2 Q16637 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
HTT P42858 1/20 0.53
ALDH1A1 P00352 4/20 0.50
KDM4E B2RXH2 1/20 0.50
GAA P10253 1/20 0.50
KMT2A Q03164 3/20 0.49
MEN1 O00255 2/20 0.49
DBH P09172 1/20 0.49
CA2 P00918 1/20 0.47
HDAC1 Q13547 2/20 0.47
HDAC6 Q9UBN7 2/20 0.47
GFER P55789 1/20 0.47
MAPK1 P28482 1/20 0.47
APOBEC3G Q9HC16 1/20 0.47
POLB P06746 1/20 0.46

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
SCHEMBL29463290 1.00 MAPT (0.56) MAPTSMN1; SMN2L3MBTL1HTTALDH1A1
SCHEMBL30413844 0.84 MAPT (0.53) MAPTSMN1; SMN2L3MBTL1HTTALDH1A1
SCHEMBL3792476 0.84 MAPT (0.53) MAPTSMN1; SMN2L3MBTL1HTTALDH1A1
SCHEMBL580639 0.83 MAPT (0.56) MAPTSMN1; SMN2L3MBTL1HTTALDH1A1
SCHEMBL29725217 0.83 CA2 (0.47) MAPTSMN1; SMN2L3MBTL1ALDH1A1KDM4E
SCHEMBL2500053 0.83 MAPT (0.56) MAPTSMN1; SMN2L3MBTL1HTTALDH1A1
SCHEMBL2296988 0.83 CA2 (0.47) MAPTSMN1; SMN2L3MBTL1ALDH1A1KDM4E
SCHEMBL29559892 0.83 CA2 (0.68) MAPTALDH1A1KDM4ECA2POLB
SCHEMBL1080853 0.83 CA2 (0.68) MAPTALDH1A1KDM4ECA2POLB
SCHEMBL2495130 0.82 HTR7 (0.58) MAPTSMN1; SMN2L3MBTL1HTTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4665339-A1 INHIBITING ALPHA V BETA 8 INTEGRIN Morphic Therapeutic, Inc. (US) 2025-12-24 EP disclosed
US-12404276-B2 Substituted pyrrolo[3,4-c]pyrazoles for treating gastric acid-related diseases SHANGHAI MEDICILON INC. (CN) 2025-09-02 US disclosed
US-20250222145-A1 TRACER COMPOSITION FOR RADIOACTIVE PET DIAGNOSIS, INTERMEDIATE THEREOF, AND PRODUCTION METHOD THEREOF OSAKA UNIVERSITY (JP) 2025-07-10 US disclosed
WO-2024173570-A1 INHIBITING αvβ8 INTEGRIN MORPHIC THERAPEUTIC, INC. (US) 2024-08-22 WO disclosed
US-20240277683-A1 COMPOUNDS CTXT PTY LTD (AU) 2024-08-22 US disclosed
US-11911372-B2 Compounds CTXT PTY LTD (AU) 2024-02-27 US disclosed
US-11911372-B2 Compounds CTXT PTY LTD (AU) 2024-02-27 US disclosed
US-11911372-B2 Compounds CTXT PTY LTD (AU) 2024-02-27 US disclosed
WO-2023063154-A1 TRACER COMPOSITION FOR RADIOACTIVE PET DIAGNOSIS, INTERMEDIATE THEREOF, AND PRODUCTION METHOD THEREOF 国立大学法人大阪大学 2023-04-20 WO disclosed
US-20220259214-A1 PYRROLOPYRAZOLE DERIVATIVES, PREPARATION METHOD THEREOF AND APPLICATION THEREOF IN MEDICINE SHANGHAI MEDICILON INC. (CN) 2022-08-18 US disclosed
US-20030153587-A1 Polycyclic guanine phosphodiesterase V inhibitors SCHERING CORPORATION 2003-08-14 US disclosed
US-6582351-B1 Benzimidazole heterocyclic compounds having pharmacological activities, and their use as a medicament for treatment or prevention of diseases mediated by cGMP-PDE FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2003-06-24 US disclosed
EP-1319003-A1 XANTHINE PHOSPHODIESTERASE V INHIBITORS SCHERING CORPORATION (US) 2003-06-18 EP disclosed
WO-2003042216-A1 POLYCYCLIC GUANINE DERIVATIVE PHOSPHODIESTERASE V INHIBITORS SCHERING CORPORATION (US) 2003-05-22 WO disclosed
WO-2003042216-A1 POLYCYCLIC GUANINE DERIVATIVE PHOSPHODIESTERASE V INHIBITORS SCHERING CORPORATION (US) 2003-05-22 WO disclosed
WO-2003020724-A1 POLYCYCLIC GUANINE PHOSPHODIESTERASE V INHIBITORS SCHERING CORPORATION (US) 2003-03-13 WO disclosed
WO-2003020724-A1 POLYCYCLIC GUANINE PHOSPHODIESTERASE V INHIBITORS SCHERING CORPORATION (US) 2003-03-13 WO disclosed
US-20020169174-A1 Xanthine phosphodiesterase V inhibitors MERCK SHARP & DOHME CORP. 2002-11-14 US disclosed
CN-1374952-A Benzimidazolone derivatives and their use as phosphodiesterase inhibibors FUJISAWA PHARMACEUTICAL CO (JP) 2002-10-16 CN disclosed
WO-2002024698-A1 XANTHINE PHOSPHODIESTERASE V INHIBITORS SCHERING CORPORATION (US) 2002-03-28 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 (7 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-20030153587-A1 Polycyclic guanine phosphodiesterase V inhibitors PDE5A, PDE3A, PDE2A MAPT 4798/4885SMN1; SMN2 3001/4885L3MBTL1 4475/4885
US-20240277683-A1 COMPOUNDS SLC10A1, ABCB11, REN MAPT 1141/4885SMN1; SMN2 998/4885L3MBTL1 4767/4885
US-20020169174-A1 Xanthine phosphodiesterase V inhibitors PDE5A, PDE3B, PDE3A MAPT 3833/4885SMN1; SMN2 3076/4885L3MBTL1 4557/4885
US-20220259214-A1 PYRROLOPYRAZOLE DERIVATIVES, PREPARATION METHOD THEREOF AND APPLICATION THEREOF IN MEDICINE PGC, ABCB11, ATP1A2 MAPT 4205/4885SMN1; SMN2 4734/4885L3MBTL1 4793/4885
US-12404276-B2 Substituted pyrrolo[3,4-c]pyrazoles for treating gastric acid-related diseases GIPR, PGC, GRPR MAPT 3777/4885SMN1; SMN2 4351/4885L3MBTL1 4318/4885
US-20250222145-A1 TRACER COMPOSITION FOR RADIOACTIVE PET DIAGNOSIS, INTERMEDIATE THEREOF, AND PRODUCTION METHOD THEREOF BCAT2, SLC7A1, BCAT1 MAPT 593/4885SMN1; SMN2 3602/4885L3MBTL1 147/4885
US-11911372-B2 Compounds SLC10A1, ABCB11, REN MAPT 1236/4885SMN1; SMN2 1164/4885L3MBTL1 4762/4885

“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.