SCHEMBL477560

SCHEMBL477560

OC(c1ccccc1)c1ccccc1Br

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 1/20 0.50
TDO2 P48775 1/20 0.50
MEN1 O00255 1/20 0.48
MAPT P10636 1/20 0.48
CYP2C9 P11712 1/20 0.48
KMT2A Q03164 1/20 0.48
CFTR P13569 2/20 0.41
OPRL1 P41146 2/20 0.41
OPRM1 P35372 1/20 0.41
OPRD1 P41143 1/20 0.41
OPRK1 P41145 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
CA1 P00915 2/20 0.39
CA2 P00918 2/20 0.39
CA9 Q16790 2/20 0.39
CA12 O43570 1/20 0.39
CA14 Q9ULX7 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.38
SLC6A4 P31645 1/20 0.38
DRD2 P14416 1/20 0.38

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
SCHEMBL17447728 1.00 IDO1 (0.50) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL3862491 1.00 IDO1 (0.50) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL8038938 0.85 CFTR (0.46) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL29930172 0.85 CFTR (0.46) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL23882867 0.84 CYP3A4 (0.43) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL11862016 0.84 CYP11B1 (0.39) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL22009838 0.84 MEN1 (0.43) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL11854000 0.84 MLKL (0.41) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL23882860 0.84 CYP3A4 (0.43) IDO1TDO2MEN1MAPTCYP2C9
SCHEMBL5377768 0.84 TSHR (0.42) IDO1TDO2MEN1MAPTCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103420747-A Synthetic method for olefin compounds SUZHOU OST ADVANCED MATERIALS CO LTD 2013-12-04 CN claimed
EP-2267064-B1 Hydrophobic fluorinated polymer surfaces UNIV MARBURG PHILIPPS (DE) 2013-06-26 EP claimed
EP-2565183-A1 Glycine transporter-1 inhibitors Amgen Inc. (US) 2013-03-06 EP claimed
EP-2859002-B1 SILICON-BASED CROSS COUPLING AGENTS AND METHODS OF THEIR USE UNIV PENNSYLVANIA (US) 2020-12-30 EP disclosed
US-9850261-B2 Silicon-based cross coupling agents and methods of their use THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2017-12-26 US disclosed
US-20170210766-A1 SILICON-BASED CROSS COUPLING AGENTS AND METHODS OF THEIR USE NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-07-27 US disclosed
US-9663476-B2 Glycine transporter-1 inhibitors AMGEN INC. (US) 2017-05-30 US disclosed
US-9499660-B2 Silicon-based cross coupling agents and methods of their use THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2016-11-22 US disclosed
CN-103420747-B The synthetic method of alkenes compounds 苏州奥索特新材料有限公司 2016-07-06 CN disclosed
WO-2016011231-A1 SILICON-BASED CROSS COUPLING AGENTS AND METHODS OF THEIR USE THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2016-01-21 WO disclosed
EP-2947067-A1 Glycine transporter-1 inhibitors Amgen, Inc (US) 2015-11-25 EP disclosed
US-20070194468-A1 Method of preparing organomagnesium compounds LUDWIG-MAXIMILIANS-UNIVERSITAT MUNCHEN (DE) 2007-08-23 US disclosed
CN-1930116-A Chiral tertiary aminoalkylnaphthols UNIV HONG KONG POLYTECHNIC (HK) 2007-03-14 CN disclosed
EP-1727783-A1 CHIRAL TERTIARY AMINOALKYLNAPHTHOLS The Hong Kong Polytechnic University (CN) 2006-12-06 EP disclosed
WO-2005087707-A1 CHIRAL TERTIARY AMINOALKYLNAPHTHOLS THE HONG KONG POLYTECHNIC UNIVERSITY (CN) 2005-09-22 WO disclosed
EP-0003923-B1 SUPPORT-ENZYME COMPLEXES AND METHOD FOR PREPARING THEM RHONE-POULENC SPECIALITES CHIMIQUES (FR) 1982-10-20 EP disclosed
US-4258133-A Enzyme-support complexes RHONE-POULENC INDUSTRIES (FR) 1981-03-24 US disclosed
EP-0003923-A1 Support-enzyme complexes and method for preparing them RHONE-POULENC SPECIALITES CHIMIQUES (FR) 1979-09-05 EP disclosed
US-3959475-A ANTIDEPRESSANT, TRANQUILIZER, ANALGESIC AMERICAN HOECHST CORPORATION (US) 1976-05-25 US disclosed
US-3957828-A 3-Aminoalkyl-1,3-dihydro-3-phenylspiro[isobenzofurans] AMERICAN HOECHST CORPORATION (US) 1976-05-18 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-20170210766-A1 SILICON-BASED CROSS COUPLING AGENTS AND METHODS OF THEIR USE RAD51, CA1, DCLRE1A IDO1 3098/4885TDO2 3205/4885MEN1 1320/4885
US-20070194468-A1 Method of preparing organomagnesium compounds SCLY, LIG3, LIG4 IDO1 220/4885TDO2 1539/4885MEN1 92/4885

“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.