SCHEMBL902429

SCHEMBL902429

CN1CCOc2cc(Br)ccc21

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP11B1 P15538 1/20 0.51
CYP11B2 P19099 1/20 0.51
NOTUM Q6P988 1/20 0.48
HTT P42858 2/20 0.46
ALDH1A1 P00352 1/20 0.46
RECQL P46063 1/20 0.46
LMNA P02545 2/20 0.46
MAPT P10636 1/20 0.46
BLM P54132 1/20 0.46
HDAC4 P56524 2/20 0.43
PTGES2 Q9H7Z7 1/20 0.42
PIK3CD O00329 3/20 0.42
PIK3CA P42336 3/20 0.42
PIK3CB P42338 3/20 0.42
PIK3CG P48736 3/20 0.42
AR P10275 1/20 0.42
PDE10A Q9Y233 1/20 0.41
HDAC3 O15379 1/20 0.39
HDAC1 Q13547 1/20 0.39
HDAC7 Q8WUI4 1/20 0.39

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
SCHEMBL30336465 1.00 CYP11B1 (0.51) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL30002805 0.87 LMNA (0.47) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL1633910 0.87 LMNA (0.47) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL154510 0.80 CYP11B1 (0.52) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL2334976 0.80 CYP11B1 (0.52) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL21605968 0.79 ALDH1A1 (0.44) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL1669818 0.79 PDE10A (0.50) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL25443617 0.79 CYP11B1 (0.51) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL6793277 0.79 CYP11B1 (0.51) CYP11B1CYP11B2NOTUMHTTALDH1A1
SCHEMBL21893788 0.79 CYP11B1 (0.51) CYP11B1CYP11B2NOTUMHTTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4663630-A1 NOVEL BENZIMIDAZOLONE DERIVATIVE COMPOUND AS AUTOTAXIN INHIBITOR LG Chem, Ltd. (KR) 2025-12-17 EP disclosed
US-20250333407-A1 Compounds and Their Use for Treatment of Hemoglobinopathies BRISTOL-MYERS SQUIBB COMPANY (US) 2025-10-30 US disclosed
US-12435128-B2 Method for predicting therapeutic effect of LSD1 inhibitor based on expression of INSM1 TAIHO PHARMACEUTICAL CO., LTD. (JP) 2025-10-07 US disclosed
US-20240327393-A1 FERROPTOSIS MODULATORS, PREPARATIONS, AND USES THEREOF Sironax Ltd. (KY) 2024-10-03 US disclosed
CN-117999259-A Iron death modulators, their preparation and use 维泰瑞隆有限公司 2024-05-07 CN disclosed
US-20230399332-A1 IMIDAZO[1,2-a]PYRAZINE OR PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE AND USE THEREOF TENCENT TECHNOLOGY (SHENZHEN) COMPANY LIMITED (CN) 2023-12-14 US disclosed
US-20230399332-A1 IMIDAZO[1,2-a]PYRAZINE OR PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE AND USE THEREOF TENCENT TECHNOLOGY (SHENZHEN) COMPANY LIMITED (CN) 2023-12-14 US disclosed
WO-2023179078-A1 IMIDAZO [1,2-A] PYRAZINE OR PYRAZOLO [1,5-A] PYRIMIDINE DERIVATIVE AND USE THEREOF 腾讯科技(深圳)有限公司 2023-09-28 WO disclosed
CN-110740991-B Novel biphenyl compound or salt thereof 大鹏药品工业株式会社 2023-07-04 CN disclosed
EP-3632443-B1 ANTI-TUMOR EFFECT POTENTIATOR USING A BIPHENYL COMPOUND TAIHO PHARMACEUTICAL CO LTD (JP) 2023-06-07 EP disclosed
EP-1458392-B1 ACRIDONES AS INHIBITORS OF IMPDH ENZYME BRISTOL MYERS SQUIBB CO (US) 2009-09-02 EP disclosed
US-20090042875-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AND USES THEREOF CELGENE CORPORATION 2009-02-12 US disclosed
US-7468446-B2 Substituted heterocyclic compounds and uses thereof CELGENE CORPORATION (US) 2008-12-23 US disclosed
US-7312209-B2 Acridone inhibitors of IMPDH enzyme BRISTOL-MYERS SQUIBB COMPANY (US) 2007-12-25 US disclosed
US-7312209-B2 Acridone inhibitors of IMPDH enzyme BRISTOL-MYERS SQUIBB COMPANY (US) 2007-12-25 US disclosed
US-7312209-B2 Acridone inhibitors of IMPDH enzyme BRISTOL-MYERS SQUIBB COMPANY (US) 2007-12-25 US disclosed
EP-1794139-A2 SUBSTITUTED HETEROCYCLIC COMPOUNDS AND USES THEREOF CELGENE CORPORATION (US) 2007-06-13 EP disclosed
WO-2006028963-A2 SUBSTITUTED HETEROCYCLIC COMPOUNDS AND USES THEREOF CELGENE CORPORATION (US) 2006-03-16 WO disclosed
US-20060052596-A1 Substituted heterocyclic compounds and uses thereof CELGENE CORPORATION 2006-03-09 US disclosed
US-20040053955-A1 Acridone inhibitors of IMPDH enzyme BRISTOL-MYERS SQUIBB COMPANY 2004-03-18 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 (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-20040053955-A1 Acridone inhibitors of IMPDH enzyme IMPDH2, IMPDH1, XDH CYP11B1 591/4885CYP11B2 460/4885NOTUM 1752/4885
US-20230399332-A1 IMIDAZO[1,2-a]PYRAZINE OR PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE AND USE THEREOF CYP2D6, UGT1A1, TPMT CYP11B1 18/4885CYP11B2 14/4885NOTUM 3931/4885
US-20060052596-A1 Substituted heterocyclic compounds and uses thereof NQO1, LTC4S, VHL CYP11B1 6/4885CYP11B2 5/4885NOTUM 611/4885
US-12435128-B2 Method for predicting therapeutic effect of LSD1 inhibitor based on expression of INSM1 INMT, CARM1, KDM1B CYP11B1 2100/4885CYP11B2 2623/4885NOTUM 1944/4885
US-20240327393-A1 FERROPTOSIS MODULATORS, PREPARATIONS, AND USES THEREOF AIFM2, GPX1, GPX4 CYP11B1 229/4885CYP11B2 210/4885NOTUM 4702/4885
US-20090042875-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AND USES THEREOF NQO1, LTC4S, VHL CYP11B1 6/4885CYP11B2 5/4885NOTUM 611/4885
US-20250333407-A1 Compounds and Their Use for Treatment of Hemoglobinopathies HBG1, HBG2, HBB CYP11B1 374/4885CYP11B2 359/4885NOTUM 4434/4885

“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.