SCHEMBL5217880

SCHEMBL5217880

COc1ccc(C(=O)C(C(=O)c2ccc(OC)cc2)c2ccccc2)cc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.63
NPC1 O15118 4/20 0.63
RAB9A P51151 4/20 0.63
POLB P06746 2/20 0.63
KMT2A Q03164 2/20 0.63
MEN1 O00255 1/20 0.63
ALDH1A1 P00352 5/20 0.59
CES2 O00748 2/20 0.59
CES1 P23141 2/20 0.59
NPSR1 Q6W5P4 2/20 0.58
PAX8 Q06710 1/20 0.58
LMNA P02545 3/20 0.56
MITF O75030 2/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
HIF1A Q16665 1/20 0.56
CYP1A2 P05177 1/20 0.56
CA1 P00915 1/20 0.55
CA2 P00918 1/20 0.55
L3MBTL1 Q9Y468 2/20 0.55
ACP3 P15309 1/20 0.53

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
SCHEMBL5215589 0.91 CES2 (0.57) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL28418656 0.89 MAPT (0.56) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL6642403 0.86 NPC1 (0.63) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL17637163 0.86 NPC1 (0.53) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL7560417 0.86 L3MBTL1 (0.66) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL23674188 0.85 NPC1 (0.61) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL812736 0.84 LMNA (0.67) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL4604321 0.84 MAPT (0.61) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL29262742 0.84 LMNA (0.67) MAPTNPC1RAB9APOLBKMT2A
SCHEMBL4604318 0.84 MAPT (0.61) MAPTNPC1RAB9APOLBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5789576-A DIASTEREOSPECIFIC DIMERIZATION USING ALKOXYMAGNESIUM HALIDE REACTANT; USED FOR SOLID PHASE SYNTHESIS OF ANTISENSE OLIGONUCLEOTIDES GENTA INCORPORATED (US) 1998-08-04 US claimed
US-5166330-A Phosphonation, amination and reaction with nucleosides HOECHST AKTIENGESELLSCHAFT (DE) 1992-11-24 US claimed
EP-0136543-B1 METHOD FOR THE PREPARATION OF NUCLEOSIDEALKYL, ARALKYL AND ARYL PHOSPHONITES AND PHOSPHONATES HOECHST AKTIENGESELLSCHAFT (DE) 1988-11-23 EP claimed
EP-0136543-A2 Method for the preparation of nucleosidealkyl, aralkyl and aryl phosphonites and phosphonates HOECHST AKTIENGESELLSCHAFT (DE) 1985-04-10 EP claimed
US-RE39708-E1 Estrogen receptor modulators CHIRON CORPORATION (US) 2007-06-26 US disclosed
EP-1102753-B1 PYRAZOLES AS ESTROGEN RECEPTOR MODULATORS NOVARTIS VACCINES & DIAGNOSTIC (US) 2007-02-28 EP disclosed
US-6727273-B2 THERAPY FOR OSTEOPOROSIS, ANTICANCER AGENTS CHIRON CORPORATION 2004-04-27 US disclosed
US-20040077701-A1 Estrogen receptor modulators CHIRON CORPORATION (US) 2004-04-22 US disclosed
US-20040034081-A9 ESTROGEN RECEPTOR MODULATORS CHIRON CORPORATION 2004-02-19 US disclosed
US-20020111374-A1 Estrogen receptor modulators CHIRON CORPORATION 2002-08-15 US disclosed
US-6291505-B1 PYRAZOLE ESTROGEN RECEPTOR AGONIST AND ANTAGONIST CHIRON CORPORATION 2001-09-18 US disclosed
EP-0592434-B1 IMPROVED PROCESS FOR THE SYNTHESIS OF OLIGOMERS GENTA INC (US) 1998-10-07 EP disclosed
EP-0592434-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF OLIGOMERS GENTA INCORPORATED (US) 1994-04-20 EP disclosed
EP-0554407-A4 1994-04-13 EP disclosed
EP-0554407-A1 NON-AROMATIC ORGANIC POLYMERIC REAGENTS FOR SOLID PHASE SYNTHESIS OF OLIGOMERS GENTA INCORPORATED (US) 1993-08-11 EP disclosed
US-5166330-A Phosphonation, amination and reaction with nucleosides HOECHST AKTIENGESELLSCHAFT (DE) 1992-11-24 US disclosed
WO-1992007882-A1 NON-AROMATIC ORGANIC POLYMERIC REAGENTS FOR SOLID PHASE SYNTHESIS OF OLIGOMERS GENTA INCORPORATED (US) 1992-05-14 WO disclosed
WO-1992007864-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF OLIGOMERS GENTA INCORPORATED (US) 1992-05-14 WO disclosed
EP-0136543-B1 METHOD FOR THE PREPARATION OF NUCLEOSIDEALKYL, ARALKYL AND ARYL PHOSPHONITES AND PHOSPHONATES HOECHST AKTIENGESELLSCHAFT (DE) 1988-11-23 EP disclosed
EP-0136543-A2 Method for the preparation of nucleosidealkyl, aralkyl and aryl phosphonites and phosphonates HOECHST AKTIENGESELLSCHAFT (DE) 1985-04-10 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 (3 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-20040077701-A1 Estrogen receptor modulators ESR1, ESR2, GPER1 MAPT 1269/4885NPC1 954/4885RAB9A 2665/4885
US-20040034081-A9 ESTROGEN RECEPTOR MODULATORS ESR1, ESR2, GPER1 MAPT 1269/4885NPC1 954/4885RAB9A 2665/4885
US-20020111374-A1 Estrogen receptor modulators ESR1, ESR2, GPER1 MAPT 1269/4885NPC1 954/4885RAB9A 2665/4885

“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.