SCHEMBL267355

SCHEMBL267355

Brc1ccc2c(c1)OCC2

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.53
MAPT P10636 1/20 0.53
HTT P42858 1/20 0.53
BLM P54132 1/20 0.53
AHR P35869 3/20 0.43
CHRM2 P08172 1/20 0.40
CHRM1 P11229 1/20 0.40
CHRNB2 P17787 1/20 0.40
CHRM3 P20309 1/20 0.40
CHRNA4 P43681 1/20 0.40
PRKCI P41743 1/20 0.39
PNMT P11086 1/20 0.38
ASIC3 Q9UHC3 1/20 0.38
KCNH2 Q12809 1/20 0.38
HDAC3 O15379 1/20 0.37
HDAC4 P56524 1/20 0.37
HDAC1 Q13547 1/20 0.37
HDAC7 Q8WUI4 1/20 0.37
HDAC2 Q92769 1/20 0.37
HDAC10 Q969S8 1/20 0.37

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
SCHEMBL30034940 0.88 LMNA (0.50) LMNAMAPTHTTBLMAHR
SCHEMBL3524411 0.88 LMNA (0.50) LMNAMAPTHTTBLMAHR
SCHEMBL3519647 0.86 MAPT (0.48) LMNAMAPTHTTBLMAHR
SCHEMBL155111 0.83 MAPT (0.53) LMNAMAPTHTTBLMAHR
SCHEMBL29584634 0.83 MAPT (0.53) LMNAMAPTHTTBLMAHR
SCHEMBL7839082 0.81 MAPT (0.52) LMNAMAPTHTTBLMAHR
SCHEMBL6725684 0.79 LMNA (0.41) LMNAMAPTHTTBLMAHR
SCHEMBL1669250 0.76 CHRM2 (0.41) MAPTCHRM2CHRM1CHRNB2CHRM3
SCHEMBL19141318 0.76 CHRM2 (0.41) MAPTCHRM2CHRM1CHRNB2CHRM3
SCHEMBL24384904 0.75 PNMT (0.53) LMNAMAPTHTTBLMAHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113122061-A Quantum dot ink and preparation method of quantum dot film TCL集团股份有限公司 2021-07-16 CN claimed
WO-2010041271-A2 PROCESS FOR PREPARATION OF (S)-N-[2-(1,6,7,8-TETRAHYDRO-2H-INDENO[5,4-B]FURAN-8-YL)ETHYL] PROPIONAMIDE AND NOVEL INTERMEDIATES THEREOF USV LIMITED (IN) 2010-04-15 WO claimed
US-20020107391-A1 Process for the synthesis of an endothelin receptor antagonist FREY LISA F (US) 2002-08-08 US claimed
WO-2026098493-A1 HETEROCYCLIC COMPOUND, PREPARATION METHOD THEREFOR, AND PHARMACEUTICAL USE THEREOF 江苏恒瑞医药股份有限公司 2026-05-15 WO disclosed
US-12612379-B2 Inhibitors of APOL1 and methods of using same VERTEX PHARMACEUTICALS INCORPORATED (US) 2026-04-28 US disclosed
EP-4720036-A1 CYP26B1 INHIBITOR COMPOUNDS AND METHODS OF USE THEREOF 16380026 Canada Inc. (CA) 2026-04-08 EP disclosed
US-12545672-B2 Antibiotic compounds, methods of manufacturing the same, pharmaceutical compositions containing the same and uses thereof DEBIOPHARM INTERNATIONAL S.A. (CH) 2026-02-10 US disclosed
US-20260035381-A1 COMPOUNDS AND COMPOSITIONS AND USES THEREOF SUMITOMO PHARMA AMERICA, INC. (US) 2026-02-05 US disclosed
US-12398130-B2 Acid addition salts of piperazine derivatives ASCENEURON SA (CH) 2025-08-26 US disclosed
US-20250221979-A1 NOVEL HETEROCYCLIC COMPOUND SHOUYAO HOLDINGS BEIJING CO LTD (CN) 2025-07-10 US disclosed
US-20250115581-A1 SUBSTITUTED PIPERIDINES AS CK1A DEGRADERS MONTE ROSA THERAPEUTICS AG (CH) 2025-04-10 US disclosed
US-20040077684-A1 Piperidinyl compounds that selectively bind integrins JANSSEN PHARMACEUTICA, NV (BE) 2004-04-22 US disclosed
WO-2004020435-A1 PIPERIDINYL COMPOUNDS THAT SELECTIVELY BIND INTEGRINS JANSSEN PHARMACEUTICA N.V. (BE) 2004-03-11 WO disclosed
WO-2004020435-A1 PIPERIDINYL COMPOUNDS THAT SELECTIVELY BIND INTEGRINS JANSSEN PHARMACEUTICA N.V. (BE) 2004-03-11 WO disclosed
CN-1129602-C 11-(substituted phenyl)-estra-4,9-diene derivatives AKZO NOBEL NV (NL) 2003-12-03 CN disclosed
US-20020107391-A1 Process for the synthesis of an endothelin receptor antagonist FREY LISA F (US) 2002-08-08 US disclosed
US-6011025-A HAVE ANTI-GLUCOCORTICOID ACTIVITY AKZO NOBEL, N.V. (NL) 2000-01-04 US disclosed
EP-0763541-B1 11-(Substituted phenyl)-estra-4,9-diene derivatives AKZO NOBEL NV (NL) 1999-07-28 EP disclosed
CN-1147520-A 11-(substituted phenyl)-estra-4,9-diene derivatives AKZO NOBEL NV (NL) 1997-04-16 CN disclosed
EP-0763541-A1 11-(Substituted phenyl)-estra-4,9-diene derivatives Akzo Nobel N.V. (NL) 1997-03-19 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 (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-20260035381-A1 COMPOUNDS AND COMPOSITIONS AND USES THEREOF ADH1C, HTR6, CNR1 LMNA 1922/4885MAPT 1213/4885HTT 128/4885
US-20250115581-A1 SUBSTITUTED PIPERIDINES AS CK1A DEGRADERS CKS1B, CSNK1A1, CKS2 LMNA 2078/4885MAPT 2308/4885HTT 4116/4885
US-12612379-B2 Inhibitors of APOL1 and methods of using same APOL1, RNASE1, LOXL1 LMNA 1246/4885MAPT 1838/4885HTT 2595/4885
US-20250221979-A1 NOVEL HETEROCYCLIC COMPOUND MAPT, MNAT1, MAT2A LMNA 876/4885MAPT 1/4885HTT 17/4885
US-20040077684-A1 Piperidinyl compounds that selectively bind integrins ITGB3, ITGAV, ITGA2B LMNA 2298/4885MAPT 3115/4885HTT 3412/4885
US-12545672-B2 Antibiotic compounds, methods of manufacturing the same, pharmaceutical compositions containing the same and uses thereof MRPL21, EMG1, RRS1 LMNA 2517/4885MAPT 4422/4885HTT 3796/4885
US-12398130-B2 Acid addition salts of piperazine derivatives DNPEP, GAA, SLC30A5 LMNA 3606/4885MAPT 3165/4885HTT 2704/4885
US-20020107391-A1 Process for the synthesis of an endothelin receptor antagonist EDNRA, EDNRB, AGTR2 LMNA 1487/4885MAPT 4506/4885HTT 2931/4885

“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.