SCHEMBL876180

SCHEMBL876180

[C]1=CCc2ccccc2C1

nearest known ligand 0.33

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.33
CYP1A2 P05177 1/20 0.31
MAOA P21397 1/20 0.30
MAOB P27338 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
SCHEMBL4502622 0.70 DRD2 (0.36) MAOAMAOB
SCHEMBL18706436 0.70
SCHEMBL20477699 0.67 TSHR (0.42) TSHRCYP1A2MAOAMAOB
SCHEMBL157430 0.67
SCHEMBL1623564 0.67
SCHEMBL1162905 0.67 TSHR (0.42) TSHRCYP1A2MAOAMAOB
SCHEMBL7205467 0.66 DRD2 (0.42) MAOB
SCHEMBL23766 0.64
SCHEMBL1162903 0.64 TSHR (0.44) TSHRCYP1A2MAOAMAOB
SCHEMBL29507678 0.64 TSHR (0.44) TSHRCYP1A2MAOAMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2961374-A1 FRAGRANCE COMPOSITIONS The Procter & Gamble Company (US) 2016-01-06 EP claimed
WO-2015089246-A1 FRAGRANCE COMPOSITIONS THE PROCTER & GAMBLE COMPANY (US) 2015-06-18 WO claimed
EP-2563508-A2 DELIVERY PARTICLE The Procter & Gamble Company (US) 2013-03-06 EP claimed
WO-2012040444-A2 TREATMENT OF PATIENTS WITH INCIPIENT ALZHEIMER'S DISEASE BRISTOL-MYERS SQUIBB COMPANY (US) 2012-03-29 WO claimed
US-7786122-B2 α-(N-sulfonamido)acetamide derivatives as β-amyloid inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2010-08-31 US claimed
WO-2010079468-A2 DELIVERY PARTICLE THE PROCTER & GAMBLE COMPANY (US) 2010-07-15 WO claimed
US-20090227492-A1 TREATMENT OF NEUROLOGICAL CONDITIONS USING COMPLEMENT C5a RECEPTOR MODULATORS WOODRUFF TRENT MARTIN 2009-09-10 US claimed
EP-1465861-B1 ALPHA-(N-SULPHONAMIDO)ACETAMIDE DERIVATIVES AS BETA-AMYLOID INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2009-05-06 EP claimed
US-20090004264-A1 METHODS FOR TREATING AND AMELIORATING THE SYMPTONS OF INFLAMMATORY BOWEL DISEASES THE UNIVERSITY OF QUEENSLAND (AU) 2009-01-01 US claimed
US-20080113904-A1 Treatment of Neurological Conditions Using Complement C5a Receptor Modulators PROMICS PTY LIMITED (AU) 2008-05-15 US claimed
US-7300936-B2 α-(N-sulfonamido)acetamide derivatives as β-amyloid inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-11-27 US claimed
CN-1997664-A Compounds that block the C5A receptor and their use in therapy ALLIGATOR BIOSCIENCE AB PUBL (SE) 2007-07-11 CN claimed
CN-1261449-C Melanocyte-stimulating hormone inhibitors AJINOMOTO KK (JP) 2006-06-28 CN claimed
EP-1465861-A4 ALPHA-(N-SULPHONAMIDO)ACETAMIDE DERIVATIVES AS BETA-AMYLOID INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2005-12-07 EP claimed
EP-1465861-A1 ALPHA-(N-SULPHONAMIDO)ACETAMIDE DERIVATIVES AS BETA-AMYLOID INHIBITORS Bristol-Myers Squibb Company (US) 2004-10-13 EP claimed
US-20040127494-A1 Alpha-(N-sulfonamido)acetamide derivatives as beta-amyloid inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-07-01 US claimed
WO-2003053912-A1 α-(N-SULPHONAMIDO)ACETAMIDE DERIVATIVES AS β-AMYLOID INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2003-07-03 WO claimed
EP-0931074-B1 CONDENSED 4,5,6,7-TETRAHYDROBENZO C]THIOPHENES AS ENHANCER FOR CELL DIFFERENTIATION INDUCTION FACTOR ACTION TAKEDA CHEMICAL INDUSTRIES LTD (JP) 2003-05-07 EP claimed
US-20020137743-A1 N-(aryl/heteroarylacetyl) amino acid esters, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds WU JING (US) 2002-09-26 US claimed
CN-1341119-A Melanocyte-stimulating hormone inhibitors AJINOMOTO KK (JP) 2002-03-20 CN claimed

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-20090004264-A1 METHODS FOR TREATING AND AMELIORATING THE SYMPTONS OF INFLAMMATORY BOWEL DISEASES C5AR2, C5AR1, C3AR1 TSHR 1425/4885CYP1A2 4108/4885MAOA 2823/4885
US-20020137743-A1 N-(aryl/heteroarylacetyl) amino acid esters, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds APP, BACE1, IAPP TSHR 3457/4885CYP1A2 2292/4885MAOA 79/4885
US-20090227492-A1 TREATMENT OF NEUROLOGICAL CONDITIONS USING COMPLEMENT C5a RECEPTOR MODULATORS C3AR1, C5AR1, C5AR2 TSHR 479/4885CYP1A2 3863/4885MAOA 1372/4885
US-20080113904-A1 Treatment of Neurological Conditions Using Complement C5a Receptor Modulators C3AR1, C5AR1, C5AR2 TSHR 479/4885CYP1A2 3863/4885MAOA 1372/4885
US-20040127494-A1 Alpha-(N-sulfonamido)acetamide derivatives as beta-amyloid inhibitors APBA1, APP, BACE1 TSHR 3640/4885CYP1A2 3492/4885MAOA 1382/4885

“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.