SCHEMBL71303

SCHEMBL71303

COC(=O)c1ccc(Nc2ccccc2)cc1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.69
MEN1 O00255 4/20 0.69
KMT2A Q03164 4/20 0.69
SMN1; SMN2 Q16637 3/20 0.69
L3MBTL1 Q9Y468 3/20 0.69
POLB P06746 1/20 0.69
MAPK13 O15264 1/20 0.62
MAPK12 P53778 1/20 0.62
MAPK11 Q15759 1/20 0.62
MAPK14 Q16539 1/20 0.62
CA1 P00915 1/20 0.62
CA2 P00918 1/20 0.62
RAB9A P51151 7/20 0.61
MAPT P10636 5/20 0.61
ALDH1A1 P00352 4/20 0.61
LMNA P02545 1/20 0.61
SIRT2 Q8IXJ6 1/20 0.61
NPC1 O15118 4/20 0.60
HPGD P15428 2/20 0.60
PTPN1 P18031 1/20 0.60

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
SCHEMBL1505883 0.92 MEN1 (0.64) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
SCHEMBL7777934 0.90 CA1 (0.60) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
Methyl Benzoate SCHEMBL28249321 0.85 TSHR (0.95) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
Benzene SCHEMBL28351738 0.85 TSHR (0.85) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
SCHEMBL4112603 0.85 MEN1 (0.75) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
SCHEMBL1745412 0.83 RAB9A (0.71) TSHRMEN1KMT2ASMN1; SMN2POLB
Methyl Benzoate SCHEMBL1332323 0.83 TSHR (1.00) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
Methyl Benzoate SCHEMBL7200 0.83 TSHR (1.00) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
Methyl Benzoate SCHEMBL29831725 0.83 TSHR (1.00) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1
Methyl Benzoate SCHEMBL1867855 0.83 TSHR (1.00) TSHRMEN1KMT2ASMN1; SMN2L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250179046-A1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS ZOETIS SERVICES LLC 2025-06-05 US disclosed
US-12240827-B2 Serotonin 5-HT2B inhibitory compounds ZOETIS SERVICES LLC (US) 2025-03-04 US disclosed
EP-3947360-B1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS ZOETIS SERVICES LLC (US) 2024-08-07 EP disclosed
CN-115073468-B Preparation and application of imidazopyrazines BTK inhibitor 药雅科技(上海)有限公司 2023-12-22 CN disclosed
CN-113631548-B Serotonin 5-HT2B inhibiting compounds 硕腾服务有限责任公司 2023-06-06 CN disclosed
US-20220162183-A1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS ZOETIS SERVICES LLC 2022-05-26 US disclosed
EP-3947360-A1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS Zoetis Services LLC (US) 2022-02-09 EP disclosed
WO-2020198478-A1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS ZOETIS SERVICES LLC (US) 2020-10-01 WO disclosed
CN-109206360-A Carbazole amide derivatives or its salt and its preparation method and application 复旦大学 2019-01-15 CN disclosed
US-10071953-B2 Bifunctional AKR1C3 inhibitors/androgen receptor modulators and methods of use thereof THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2018-09-11 US disclosed
EP-2268143-A2 NOVEL PIPERIDINE DERIVATIVES AS INHIBITORS OF STEAROYL-COA DESATURASE Forest Laboratories Holdings Limited (BM) 2011-01-05 EP disclosed
WO-2010075356-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-COA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-07-01 WO disclosed
WO-2010075356-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-COA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-07-01 WO disclosed
US-20100160323-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-06-24 US disclosed
US-20100160323-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-06-24 US disclosed
US-20100160323-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-06-24 US disclosed
WO-2009117676-A2 NOVEL PIPERIDINE DERIVATIVES AS INHIBITORS OF STEAROYL-COA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2009-09-24 WO disclosed
US-20090239810-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2009-09-24 US disclosed
US-6069149-A ANTIALLERGENS, ANTIINFLAMMATORY AGENTS TERUMO KABUSHIKI KAISHA (JP) 2000-05-30 US disclosed
EP-0894797-A1 NOVEL AMIDE DERIVATIVES AND INTERMEDIATES FOR THE SYNTHESIS THEREOF TERUMO KABUSHIKI KAISHA (JP) 1999-02-03 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 (6 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-12240827-B2 Serotonin 5-HT2B inhibitory compounds HTR2B, HTR1B, HTR5A TSHR 786/4885MEN1 240/4885KMT2A 2893/4885
US-20220162183-A1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS HTR2B, HTR1B, HTR5A TSHR 786/4885MEN1 240/4885KMT2A 2893/4885
US-10071953-B2 Bifunctional AKR1C3 inhibitors/androgen receptor modulators and methods of use thereof AR, AKR1C3, AKR1C2 TSHR 1463/4885MEN1 3949/4885KMT2A 1290/4885
US-20100160323-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE SCD, SCD5, FADS2 TSHR 4601/4885MEN1 4883/4885KMT2A 1389/4885
US-20250179046-A1 SEROTONIN 5-HT2B INHIBITORY COMPOUNDS HTR2B, HTR1B, HTR5A TSHR 786/4885MEN1 240/4885KMT2A 2893/4885
US-20090239810-A1 NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE SCD, SCD5, FADS2 TSHR 4631/4885MEN1 4884/4885KMT2A 1352/4885

“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.