SCHEMBL976424

SCHEMBL976424

COC(=O)c1cccc(OCc2ccccc2)c1

nearest known ligand 0.73

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
MAOB P27338 2/20 0.73
NR4A2 P43354 2/20 0.72
MRGPRX4 Q96LA9 3/20 0.71
SMPD1 P17405 3/20 0.69
PTPN1 P18031 1/20 0.66
SRD5A2 P31213 1/20 0.63
LMNA P02545 1/20 0.62
HPGD P15428 1/20 0.62
CYSLTR1 Q9Y271 1/20 0.61
MEN1 O00255 1/20 0.61
KMT2A Q03164 1/20 0.61
NR1H4 Q96RI1 1/20 0.60
GPR132 Q9UNW8 1/20 0.59

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
SCHEMBL30412034 1.00 MAOB (0.73) MAOBNR4A2MRGPRX4SMPD1PTPN1
SCHEMBL1122805 0.97 MRGPRX4 (0.71) MAOBNR4A2MRGPRX4SMPD1PTPN1
SCHEMBL1122722 0.96 MAOB (0.68) MAOBNR4A2MRGPRX4SMPD1PTPN1
SCHEMBL10411878 0.92 MRGPRX4 (0.77) MAOBNR4A2MRGPRX4SMPD1CYSLTR1
SCHEMBL1171850 0.92 MRGPRX4 (0.65) MAOBNR4A2MRGPRX4SMPD1PTPN1
SCHEMBL28768851 0.89 MAOB (0.58) MAOBNR4A2MRGPRX4SMPD1PTPN1
SCHEMBL2254423 0.88 SMPD1 (0.76) MAOBNR4A2MRGPRX4SMPD1LMNA
SCHEMBL2654709 0.88 MRGPRX4 (0.71) MAOBNR4A2MRGPRX4SMPD1CYSLTR1
SCHEMBL391547 0.88 MEN1 (0.71) MAOBNR4A2MRGPRX4SMPD1PTPN1
SCHEMBL183994 0.88 LMNA (0.70) MAOBNR4A2MRGPRX4SMPD1PTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090264412-A1 Combination Therapy Using An 11beta-Hydroxysteroid Dehydrogenase Type 1 Inhibitor And A Glucocorticoid Receptor Agonist To Minimize The Side Effects Associated With Glucocorticoid Receptor Agonist Therapy HIGH POINT PHARMACEUTICALS, LLC (US) 2009-10-22 US claimed
US-20090137574-A1 Combination Therapy Using an 11Beta-Hydroxysteroid Dehydrogenase Type 1 Inhibitor and an Antihypertensive Agent for the Treatment of Metabolic Syndrome and Related Diseases and Disorders NOVO NORDISK A/S (DK) 2009-05-28 US claimed
US-20070270408-A1 Pharmaceutical use of substituted pyrazolo[1,5-a]pyrimidines NOVO NORDISK A/S (DK) 2007-11-22 US claimed
EP-1782859-A2 Pharmaceutical use of substituted pyrazolo [1,5- a]pyrimidines NOVO NORDISK A/S (DK) 2007-05-09 EP claimed
US-20060111348-A1 Combination therapy using an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent for the treatment of metabolic syndrome and related diseases and disorders NOVO NORDISK A/S (DK) 2006-05-25 US claimed
US-20060094699-A1 Combination therapy using an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and a glucocorticoid receptor agonist to minimize the side effects associated with glucocorticoid receptor agonist therapy HIGH POINT PHARMACEUTICALS, LLC 2006-05-04 US claimed
EP-1615666-A2 COMBINATION OF AN 11BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND AN ANTIHYPERTENSIVE AGENT NOVO NORDISK A/S (DK) 2006-01-18 EP claimed
WO-2004089416-A2 COMBINATION OF AN 11BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND AN ANTIHYPERTENSIVE AGENT NOVO NORDISK A/S (DK) 2004-10-21 WO claimed
US-12600703-B2 Methods of synthesizing farnesyl dibenzodiazepinones AMO PHARMA LTD. (GB) 2026-04-14 US disclosed
US-12534457-B2 Heteroaryl derivative compounds, and uses thereof VORONOI INC. (KR) 2026-01-27 US disclosed
US-12528799-B2 Heteroaryl derivative compounds, and uses thereof VORONOI INC. (KR) 2026-01-20 US disclosed
US-20240317730-A1 HETEROARYL DERIVATIVE COMPOUNDS, AND USES THEREOF VORONOI INC. (KR) 2024-09-26 US disclosed
US-20240262815-A1 HETEROARYL DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME AS ACTIVE INGREDIENT VORONOI INC (KR) 2024-08-08 US disclosed
US-12037330-B2 Heteroaryl derivative compounds, and uses thereof VORONOI INC. (KR) 2024-07-16 US disclosed
EP-0049953-B1 4-(SUBSTITUTED PHENYL)-NAPHTHALEN-2(1H)-ONES AND 2-OLS, PROCESSES FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM PFIZER INC. (US) 1984-05-16 EP disclosed
EP-0079168-A1 Process for making 1-(3-benzyloxyphenyl)-1,1-dimethylheptane and intermediates therefor PFIZER INC. (US) 1983-05-18 EP disclosed
US-4360700-A Intermediates for making 1-(3-benzyloxyphenyl)-1,1-dimethylheptane PFIZER INC. (US) 1982-11-23 US disclosed
US-4331602-A CNS AGENTS, ANTIEMETICS, ANTIDIARRHEA PFIZER INC. (US) 1982-05-25 US disclosed
EP-0049953-A2 4-(Substituted phenyl)-naphthalen-2(1H)-ones and 2-ols, processes for their preparation, and pharmaceutical compositions containing them PFIZER INC. (US) 1982-04-21 EP disclosed
US-4285867-A ANTIDIARRHEA AGENTS, ANTIEMETICS, ANALGESICS PFIZER INC. (US) 1981-08-25 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 (11 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-12037330-B2 Heteroaryl derivative compounds, and uses thereof ERBB2, EGFR, ERBB3 MAOB 1885/4885NR4A2 1988/4885MRGPRX4 2888/4885
US-20070270408-A1 Pharmaceutical use of substituted pyrazolo[1,5-a]pyrimidines HSD3B1, HSD11B1, SRD5A1 MAOB 1128/4885NR4A2 1656/4885MRGPRX4 1293/4885
US-20060094699-A1 Combination therapy using an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and a glucocorticoid receptor agonist to minimize the side effects associated with glucocorticoid receptor agonist therapy HSD11B1, HSD17B1, NR3C1 MAOB 2397/4885NR4A2 129/4885MRGPRX4 334/4885
US-20090137574-A1 Combination Therapy Using an 11Beta-Hydroxysteroid Dehydrogenase Type 1 Inhibitor and an Antihypertensive Agent for the Treatment of Metabolic Syndrome and Related Diseases and Disorders HSD11B1, HSD11B2, HSD17B1 MAOB 599/4885NR4A2 2025/4885MRGPRX4 2259/4885
US-20060111348-A1 Combination therapy using an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent for the treatment of metabolic syndrome and related diseases and disorders HSD11B1, HSD11B2, HSD17B1 MAOB 599/4885NR4A2 2025/4885MRGPRX4 2259/4885
US-20240262815-A1 HETEROARYL DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME AS ACTIVE INGREDIENT ERBB2, ERBB4, ERBB3 MAOB 3672/4885NR4A2 152/4885MRGPRX4 2406/4885
US-20240317730-A1 HETEROARYL DERIVATIVE COMPOUNDS, AND USES THEREOF ERBB2, EGFR, ERBB3 MAOB 1885/4885NR4A2 1988/4885MRGPRX4 2888/4885
US-20090264412-A1 Combination Therapy Using An 11beta-Hydroxysteroid Dehydrogenase Type 1 Inhibitor And A Glucocorticoid Receptor Agonist To Minimize The Side Effects Associated With Glucocorticoid Receptor Agonist Therapy HSD11B1, HSD17B1, NR3C1 MAOB 2397/4885NR4A2 129/4885MRGPRX4 334/4885
US-12528799-B2 Heteroaryl derivative compounds, and uses thereof ERBB2, EGFR, ERBB3 MAOB 3077/4885NR4A2 267/4885MRGPRX4 903/4885
US-12534457-B2 Heteroaryl derivative compounds, and uses thereof ERBB2, EGFR, ERBB3 MAOB 2014/4885NR4A2 2421/4885MRGPRX4 2466/4885
US-12600703-B2 Methods of synthesizing farnesyl dibenzodiazepinones NR1H2, NR1H3, NR1H4 MAOB 2969/4885NR4A2 715/4885MRGPRX4 1258/4885

“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.