SCHEMBL482928

SCHEMBL482928

CC(C)(N)Cc1ccc(Cl)c(F)c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 P23975 2/20 0.55
SLC6A3 Q01959 2/20 0.55
HTR2A P28223 1/20 0.55
SLC6A4 P31645 1/20 0.55
HRH1 P35367 1/20 0.55
HTR2B P41595 1/20 0.55
CHRNA4 P43681 1/20 0.55
TAAR1 Q96RJ0 2/20 0.44
PNMT P11086 2/20 0.37
MAPT P10636 2/20 0.36
MAPK1 P28482 1/20 0.36
ANO1 Q5XXA6 1/20 0.36
IDO1 P14902 2/20 0.34
FDPS P14324 1/20 0.34
GRM2 Q14416 1/20 0.34
QPCT Q16769 2/20 0.33
RAPGEF4 Q8WZA2 1/20 0.33
QPCTL Q9NXS2 1/20 0.33
KDM4E B2RXH2 1/20 0.33
MEN1 O00255 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
SCHEMBL9917330 0.85 ESR1 (0.42) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL562364 0.82 SLC6A2 (0.55) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL12215710 0.82 SLC6A2 (0.61) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL15546805 0.81 ANO1 (0.41) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL13592379 0.81 FDPS (0.41) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL13144963 0.80 ANO1 (0.36) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL13509548 0.80 PNMT (0.36) TAAR1PNMTMAPTMAPK1ANO1
SCHEMBL1555419 0.79 SLC6A2 (0.47) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL1720743 0.79 IDO1 (0.58) SLC6A2SLC6A3HTR2ASLC6A4HRH1
SCHEMBL16589323 0.79 ANO1 (0.38) PNMTMAPTMAPK1ANO1FDPS

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2875001-B1 NITROGENOUS HETEROCYCLIC DERIVATIVES AND THEIR APPLICATION IN DRUGS SUNSHINE LAKE PHARMA CO LTD (CN) 2019-01-09 EP disclosed
US-9434695-B2 Nitrogenous heterocyclic derivatives and their application in drugs SUNSHINE LAKE PHARMA CO., LTD (CN) 2016-09-06 US disclosed
EP-2875001-A1 NITROGENOUS HETEROCYCLIC DERIVATIVES AND THEIR APPLICATION IN DRUGS Sunshine Lake Pharma Co., Ltd. (CN) 2015-05-27 EP disclosed
US-20150087639-A1 Nitrogenous Heterocyclic Derivatives And Their Application In Drugs SUNSHINE LAKE PHARMA CO., LTD. (CN) 2015-03-26 US disclosed
WO-2014012360-A1 NITROGENOUS HETEROCYCLIC DERIVATIVES AND THEIR APPLICATION IN DRUGS SUNSHINE LAKE PHARMA CO., LTD. (CN) 2014-01-23 WO disclosed
US-20120301552-A1 CaSR Antagonist JAPAN TOBACCO INC. (JP) 2012-11-29 US disclosed
US-20120301552-A1 CaSR Antagonist JAPAN TOBACCO INC. (JP) 2012-11-29 US disclosed
US-20120301552-A1 CaSR Antagonist JAPAN TOBACCO INC. (JP) 2012-11-29 US disclosed
CN-102365261-A Process for producing carboxylic acid compound JAPAN TOBACCO INC 2012-02-29 CN disclosed
EP-2412697-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID COMPOUND Japan Tobacco, Inc. (JP) 2012-02-01 EP disclosed
WO-2009148052-A1 SULFONAMIDE COMPOUND AND APPLICATION THEREOF 旭化成ファーマ株式会社 (JP) 2009-12-10 WO disclosed
EP-2120898-A1 CALCILYTIC COMPOUNDS SmithKline Beecham Corporation (US) 2009-11-25 EP disclosed
US-20080255042-A1 CaSR Antagonist JAPAN TOBACCO INC. (JP) 2008-10-16 US disclosed
US-20080255042-A1 CaSR Antagonist JAPAN TOBACCO INC. (JP) 2008-10-16 US disclosed
WO-2008077009-A1 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2008-06-26 WO disclosed
US-7304174-B2 CaSR antagonist JAPAN TOBACCO INC. (JP) 2007-12-04 US disclosed
US-7304174-B2 CaSR antagonist JAPAN TOBACCO INC. (JP) 2007-12-04 US disclosed
US-7304174-B2 CaSR antagonist JAPAN TOBACCO INC. (JP) 2007-12-04 US disclosed
EP-1619180-A1 CaSR ANTAGONIST JAPAN TOBACCO INC. (JP) 2006-01-25 EP disclosed
US-20050032796-A1 Compounds as for example, 2'-[1-[(2R)-3-[[1-(3-fluoro-4-methylphenyl)-2-methylpropan-2-yl]amino]-2-hydroxypropoxy]ethyl]-3-methylbiphenyl-4-carboxylic acid, having a calcium-sensing receptor antagonistic action; therapeutic drug for osteoporosis JAPAN TOBACCO INC. 2005-02-10 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 (4 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-20150087639-A1 Nitrogenous Heterocyclic Derivatives And Their Application In Drugs TNNC1, TNNI3, IAPP SLC6A2 1354/4885SLC6A3 1274/4885HTR2A 2764/4885
US-20120301552-A1 CaSR Antagonist CASR, CALCR, CALCRL SLC6A2 1201/4885SLC6A3 1529/4885HTR2A 1085/4885
US-20080255042-A1 CaSR Antagonist CASR, CALCR, CALCRL SLC6A2 1201/4885SLC6A3 1529/4885HTR2A 1085/4885
US-20050032796-A1 Compounds as for example, 2'-[1-[(2R)-3-[[1-(3-fluoro-4-methylphenyl)-2-methylpropan-2-yl]amino]-2-hydroxypropoxy]ethyl]-3-methylbiphenyl-4-carboxylic acid, having a calcium-sensing receptor antagonistic action; therapeutic drug for osteoporosis CASR, CALCR, GRK2 SLC6A2 1989/4885SLC6A3 2358/4885HTR2A 499/4885

“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.