SCHEMBL1751841

SCHEMBL1751841

CC(C)(C)[Si](C)(C)n1cc(Br)c2ccccc21

nearest known ligand 0.32

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
GPR3 P46089 1/20 0.32
SMN1; SMN2 Q16637 2/20 0.32
KDM4E B2RXH2 1/20 0.32
NPC1 O15118 1/20 0.32
ALDH1A1 P00352 1/20 0.32
CYP1A2 P05177 1/20 0.32
CYP3A4 P08684 1/20 0.32
CYP2D6 P10635 1/20 0.32
HPGD P15428 1/20 0.32
RAB9A P51151 1/20 0.32
IMPDH2 P12268 1/20 0.31
HTR6 P50406 2/20 0.31
GPR84 Q9NQS5 1/20 0.30
MAPK10 P53779 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30
RXFP1 Q9HBX9 1/20 0.30

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
SCHEMBL1752166 0.79 GPR3 (0.32) GPR3SMN1; SMN2KDM4ENPC1ALDH1A1
SCHEMBL5511626 0.78 GRM2 (0.32)
SCHEMBL30776600 0.78 GRM2 (0.32)
SCHEMBL29957339 0.77 MAPT (0.32) GPR3SMN1; SMN2KDM4ENPC1ALDH1A1
SCHEMBL3450325 0.77 MAPT (0.32) GPR3SMN1; SMN2KDM4ENPC1ALDH1A1
SCHEMBL3450328 0.74 KDM4E (0.31) KDM4EALDH1A1HPGD
SCHEMBL29830999 0.74 GPR3 (0.33) GPR3SMN1; SMN2HPGDHTR6GPR84
SCHEMBL1077030 0.74 GPR3 (0.33) GPR3SMN1; SMN2HPGDHTR6GPR84
SCHEMBL29957737 0.71 ALDH1A1 (0.33) ALDH1A1IMPDH2
SCHEMBL5016700 0.71

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130253201-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED CYCLIC BETA-ARYL OR HETEROARYL CARBOCYCLIC ACIDS HOFFMANN-LA ROCHE INC. (US) 2013-09-26 US disclosed
CN-101460461-B Process for preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carboxylic acids HOFFMANN LA ROCHE 2012-10-03 CN disclosed
US-20110105758-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED CYCLIC BETA-ARYL OR HETEROARYLCARBOCYCLIC ACIDS BACHMANN STEPHAN 2011-05-05 US disclosed
EP-2029541-B1 PROCESS FOR PREPARATION OF ENANTIOMERICALLY ENRICHED CYCLIC BETA-ARYL OR HETEROARYL CARBOXYLIC ACIDS HOFFMANN LA ROCHE (CH) 2009-12-30 EP disclosed
CN-101460461-A Process for preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carboxylic acids HOFFMANN LA ROCHE (CH) 2009-06-17 CN disclosed
CN-100408575-C Aryl-8-azabicyclo[3,2,1]octanes for treating depression WYETH CORP (US) 2008-08-06 CN disclosed
US-20070232653-A1 Process for the preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carbocyclic acids HOFFMANN-LA ROCHE INC. 2007-10-04 US disclosed
US-7060830-B2 Synthesized γ-carbolines GEORGE MASON INTELLECTUAL PROPERTIES, INC. (US) 2006-06-13 US disclosed
US-20050176759-A1 7-sulfonyl-3-benzazepine derivatives as modulators of the dopamine receptor and their use for the treatment cns disorders SMITHKLINE BEECHAM P.L.C. (GB) 2005-08-11 US disclosed
US-20050131010-A1 Synthesized gamma-carbolines WYNNE JAMES H (US) 2005-06-16 US disclosed
US-6872830-B1 Synthesized γ-carbolines GEORGE MASON UNIVERSITY (US) 2005-03-29 US disclosed
EP-1390364-B1 ARYL-8-AZABICYCLO 3.2.1]OCTANES FOR THE TREATMENT OF DEPRESSION WYETH CORP (US) 2004-09-29 EP disclosed
CN-1509287-A Aryl-8-azabicyclo[3,2,1]octanes for treating depression 2004-06-30 CN disclosed
US-6632824-B2 Have the ability to act at the 5-HT transporter. WYETH 2003-10-14 US disclosed
US-20030032645-A1 Aryl-8-azabicyclo [3.2.1] octanes for the treatment of depression WYETH 2003-02-13 US disclosed
EP-1021423-A1 MACROCYCLIC INHIBITORS OF MATRIX METALLOPROTEINASES AND TNF$g(a) SECRETION Abbott Laboratories (US) 2000-07-26 EP disclosed
US-5952320-A USEFUL IN THE TREATMENT OF DISEASES IN WHICH MATRIX METALLOPROTEINASE PLAY A ROLE; MATRIX METALLOPROTEINASE INHIBITING COMPOSITIONS ABBOTT LABORATORIES (US) 1999-09-14 US disclosed
WO-1998030551-A1 MACROCYCLIC INHIBITORS OF MATRIX METALLOPROTEINASES AND TNFα SECRETION ABBOTT LABORATORIES (US) 1998-07-16 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 (6 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-20110105758-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED CYCLIC BETA-ARYL OR HETEROARYLCARBOCYCLIC ACIDS AHR, AR, CYP8B1 GPR3 1041/4885SMN1; SMN2 4520/4885KDM4E 4079/4885
US-20030032645-A1 Aryl-8-azabicyclo [3.2.1] octanes for the treatment of depression HTR1A, HTR1D, HTR2C GPR3 341/4885SMN1; SMN2 3226/4885KDM4E 404/4885
US-20050176759-A1 7-sulfonyl-3-benzazepine derivatives as modulators of the dopamine receptor and their use for the treatment cns disorders MPL, HTR2B, PDGFRB GPR3 206/4885SMN1; SMN2 491/4885KDM4E 2679/4885
US-20130253201-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED CYCLIC BETA-ARYL OR HETEROARYL CARBOCYCLIC ACIDS AHR, CYP8B1, ADRA2C GPR3 749/4885SMN1; SMN2 4529/4885KDM4E 4211/4885
US-20050131010-A1 Synthesized gamma-carbolines SNCA, PARK7, PRNP GPR3 948/4885SMN1; SMN2 1121/4885KDM4E 1744/4885
US-20070232653-A1 Process for the preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carbocyclic acids AHR, CYP8B1, ADRA2C GPR3 749/4885SMN1; SMN2 4529/4885KDM4E 4211/4885

“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.