SCHEMBL2499200

SCHEMBL2499200

COc1ccc(SCC(=O)c2ccccc2)cc1OC

nearest known ligand 0.60

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.60
ALDH1A1 P00352 5/20 0.60
SMN1; SMN2 Q16637 2/20 0.60
LMNA P02545 2/20 0.58
RAB9A P51151 2/20 0.58
HSD11B1 P28845 5/20 0.52
GAA P10253 2/20 0.50
NPC1 O15118 2/20 0.50
HTT P42858 1/20 0.50
POLB P06746 2/20 0.49
TRPM5 Q9NZQ8 1/20 0.49
KDM4E B2RXH2 1/20 0.49
TSHR P16473 1/20 0.49
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
RXFP1 Q9HBX9 1/20 0.48

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
SCHEMBL8597038 0.90 TSHR (0.56) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL6280285 0.90 MAPT (0.54) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL7455682 0.89 RAB9A (0.51) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL5685561 0.88 ALDH1A1 (0.56) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL6281258 0.88 MAPT (0.56) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL7455153 0.88 SMPD1 (0.57) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL28500412 0.87 MAPT (0.67) MAPTALDH1A1SMN1; SMN2RAB9AHSD11B1
SCHEMBL342810 0.82 ALDH1A1 (0.53) MAPTALDH1A1SMN1; SMN2LMNAGAA
SCHEMBL2395083 0.81 ALDH1A1 (0.65) MAPTALDH1A1SMN1; SMN2LMNARAB9A
SCHEMBL11599893 0.81 ALDH1A1 (0.59) MAPTALDH1A1SMN1; SMN2LMNARAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2011132194-A1 PROCESS FOR THE PREPARATION OF RALOXIFENE HYDROCHLORIDE HETERO RESEARCH FOUNDATION (IN) 2011-10-27 WO claimed
WO-2011132194-A1 PROCESS FOR THE PREPARATION OF RALOXIFENE HYDROCHLORIDE HETERO RESEARCH FOUNDATION (IN) 2011-10-27 WO disclosed
WO-2011132194-A1 PROCESS FOR THE PREPARATION OF RALOXIFENE HYDROCHLORIDE HETERO RESEARCH FOUNDATION (IN) 2011-10-27 WO disclosed
US-8030330-B2 Benzothiophenes, formulations containing same, and methods ELI LILLY AND COMPANY (US) 2011-10-04 US disclosed
US-20100255106-A1 BENZOTHIOPHENES, FORMULATIONS CONTAINING SAME, AND METHODS ARBUTHNOT GORDON NELSON 2010-10-07 US disclosed
WO-2005003116-A9 PROCESS FOR PREPARING RALOXIFENE HYDROCHLORIDE ERREGIERRE SPA (IT) 2008-09-25 WO disclosed
EP-1641773-B1 PROCESS FOR PREPARING RALOXIFENE HYDROCHLORIDE ERREGIERRE SPA (IT) 2008-07-23 EP disclosed
US-20070100147-A1 Process for preparing raloxifene hydrochloride ERREGIERRE S.P.A (IT) 2007-05-03 US disclosed
EP-1641773-A1 PROCESS FOR PREPARING RALOXIFENE HYDROCHLORIDE ERREGIERRE S.p.A. (IT) 2006-04-05 EP disclosed
US-7012153-B2 Process for preparing benzoic acids ELI LILLY AND COMPANY (US) 2006-03-14 US disclosed
US-4656187-A SYNERGISTIC COMBINATION ELI LILLY AND COMPANY (US) 1987-04-07 US disclosed
EP-0062504-B1 PROCESS FOR PREPARING 3-(4-AMINOETHOXYBENZOYL)BENZO(B)THIOPHENES ELI LILLY AND COMPANY (US) 1986-01-02 EP disclosed
EP-0062505-B1 A PROCESS FOR PREPARING ACYLATED BENZOTHIOPHENES ELI LILLY AND COMPANY (US) 1985-07-24 EP disclosed
US-4418068-A Antiestrogenic and antiandrugenic benzothiophenes ELI LILLY AND COMPANY (US) 1983-11-29 US disclosed
US-4380635-A Synthesis of acylated benzothiophenes ELI LILLY AND COMPANY (US) 1983-04-19 US disclosed
US-4358593-A BY ACYLATION OF PROTECTED 6-HYDROXY,2-(4-HYDROXYPHENYL) BENZO (B)THIOPHENE USING A FRIEDEL CRAFTS CATALYSTS; HYDROLYSIS ELI LILLY AND COMPANY (US) 1982-11-09 US disclosed
EP-0062503-A1 Benzothiophene compounds and process for preparing them ELI LILLY AND COMPANY (US) 1982-10-13 EP disclosed
EP-0062504-A1 Process for preparing 3-(4-aminoethoxybenzoyl)benzo(b)thiophenes ELI LILLY AND COMPANY (US) 1982-10-13 EP disclosed
EP-0062505-A1 A process for preparing acylated benzothiophenes ELI LILLY AND COMPANY (US) 1982-10-13 EP disclosed
US-4133814-A ANTITUMOR AGENTS ELI LILLY AND COMPANY (US) 1979-01-09 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 (2 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-20070100147-A1 Process for preparing raloxifene hydrochloride KAT2A, ADH1A, KAT2B MAPT 4172/4885ALDH1A1 152/4885SMN1; SMN2 4028/4885
US-20100255106-A1 BENZOTHIOPHENES, FORMULATIONS CONTAINING SAME, AND METHODS BRCA1, CYP19A1, CYP46A1 MAPT 109/4885ALDH1A1 1786/4885SMN1; SMN2 3033/4885

“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.