SCHEMBL6086554

SCHEMBL6086554

COc1cc2c(cc1C)CCCC2(C)C

nearest known ligand 0.46

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
RXRA P19793 5/20 0.46
RXRB P28702 2/20 0.46
RXRG P48443 2/20 0.46
POLA1 P09884 2/20 0.37
KDM1A O60341 1/20 0.36
ALOX15 P16050 1/20 0.36
TAAR1 Q96RJ0 1/20 0.34
ALDH1A1 P00352 1/20 0.34
MAPK1 P28482 1/20 0.34
CYP3A4 P08684 1/20 0.34
CYP11B1 P15538 1/20 0.34
CYP11B2 P19099 1/20 0.34
KDM4E B2RXH2 1/20 0.33

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
SCHEMBL30573101 0.93 RXRA (0.46) RXRARXRBRXRGPOLA1KDM1A
SCHEMBL26607136 0.93 RXRA (0.46) RXRARXRBRXRGPOLA1KDM1A
SCHEMBL4654263 0.90 RXRA (0.37) RXRARXRBRXRGPOLA1TAAR1
SCHEMBL1496270 0.83 MAPT (0.38) RXRARXRBRXRGALDH1A1MAPK1
SCHEMBL6085848 0.82 HTR2A (0.46) RXRARXRBRXRGPOLA1
SCHEMBL8293241 0.78 RXRA (0.51) RXRARXRBRXRGTAAR1
SCHEMBL5706367 0.78 RXRA (0.40) RXRARXRBRXRG
SCHEMBL6275679 0.77 RXRA (0.47) RXRARXRBRXRGPOLA1
SCHEMBL6785200 0.77 MAPT (0.46) RXRAALDH1A1MAPK1CYP3A4KDM4E
SCHEMBL5706327 0.76 RXRA (0.51) RXRARXRBRXRGPOLA1ALOX15

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7947671-B2 Synthesis of naturally occuring ecteinascidins and related compounds PHARMA MAR, S.A. (ES) 2011-05-24 US disclosed
US-7795260-B2 Synthesis of naturally occurring ecteinascidins and related compounds PHARMA MAR, S.A. (ES) 2010-09-14 US disclosed
US-20100216987-A1 SYNTHESIS OF NATURALLY OCCURING ECTEINASCIDINS AND RELATED COMPOUNDS BARRASA VALENTIN MARTINEZ 2010-08-26 US disclosed
US-7767659-B2 Synthesis of naturally occurring ecteinascidins and related compounds PHARMA MAR, S.A. (ES) 2010-08-03 US disclosed
US-20090163507-A1 SYNTHESIS OF NATURALLY OCCURING ECTEINASCIDINS AND RELATED COMPOUNDS PHARMA MAR, S.A. (ES) 2009-06-25 US disclosed
US-20070093658-A1 Synthesis of naturally occcuring ecteinascidins and related compounds PHARMA MAR, S.A. (ES) 2007-04-26 US disclosed
US-7026487-B2 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, a pyridyl group and an alkyl group, having retinoid-like biological activity ALLERGAN, INC. (US) 2006-04-11 US disclosed
EP-1401427-A4 NON-PEPTIDE GNRH AGENTS, PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THEIR USES, AND PROCESSES FOR PREPARING THEM AGOURON PHARMA (US) 2004-12-01 EP disclosed
US-20040097733-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity BEARD RICHARD L (US) 2004-05-20 US disclosed
EP-1401427-A2 NON-PEPTIDE GNRH AGENTS, PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THEIR USES, AND PROCESSES FOR PREPARING THEM Agouron Pharmaceuticals, Inc. (US) 2004-03-31 EP disclosed
US-20030166932-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity ALLERGAN SALES, INC. 2003-09-04 US disclosed
US-6613917-B1 Retinoid agonist, antagonist or negative hormone-like biological activity ALLERGAN, INC. 2003-09-02 US disclosed
EP-1265848-A2 AMINES SUBSTITUTED WITH A DIHYDRONAPHTHALENYL, CRHOMENYL, OR THIOCHROMENYL GROUP, AN ARYL OR HETEROARYL GROUP AND AN ALKYL GROUP, HAVING RETINOID-LIKE BIOLOGICAL ACTIVITY Allergan Sales, Inc. (US) 2002-12-18 EP disclosed
WO-2002098363-A2 NON-PEPTIDE GnRH AGENTS, PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THEIR USES, AND PROCESSES FOR PREPARING THEM AGOURON PHARMACEUTICALS, INC. (US) 2002-12-12 WO disclosed
WO-2001070668-A2 AMINES SUBSTITUTED WITH A DIHYDRONAPHTHALENYL, CRHOMENYL, OR THIOCHROMENYL GROUP, AN ARYL OR HETEROARYL GROUP AND AN ALKYL GROUP, HAVING RETINOID-LIKE BIOLOGICAL ACTIVITY ALLERGAN, INC. (US) 2001-09-27 WO 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 (5 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-20100216987-A1 SYNTHESIS OF NATURALLY OCCURING ECTEINASCIDINS AND RELATED COMPOUNDS NQO1, HCCS, NME1 RXRA 3053/4885RXRB 2976/4885RXRG 2402/4885
US-20070093658-A1 Synthesis of naturally occcuring ecteinascidins and related compounds NQO1, EDF1, RCN1 RXRA 3270/4885RXRB 2972/4885RXRG 2161/4885
US-20090163507-A1 SYNTHESIS OF NATURALLY OCCURING ECTEINASCIDINS AND RELATED COMPOUNDS NQO1, HCCS, NME1 RXRA 3053/4885RXRB 2976/4885RXRG 2402/4885
US-20030166932-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity NR4A1, NR2E3, NR0B1 RXRA 13/4885RXRB 12/4885RXRG 17/4885
US-20040097733-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity NR4A1, NR2E3, NR0B1 RXRA 13/4885RXRB 12/4885RXRG 17/4885

“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.