SCHEMBL43344

SCHEMBL43344

CN(C)CCc1cccc(O)c1

nearest known ligand 0.66

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 5/20 0.66
DRD3 P35462 4/20 0.66
DRD1 P21728 2/20 0.66
DRD4 P21917 1/20 0.66
DRD5 P21918 1/20 0.66
OPRK1 P41145 11/20 0.65
TAAR1 Q96RJ0 5/20 0.61
OPRM1 P35372 10/20 0.60
OPRD1 P41143 10/20 0.60
CHRM2 P08172 1/20 0.56
CHRM1 P11229 1/20 0.56
CHRM3 P20309 1/20 0.56

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
Hydrochloric Acid SCHEMBL4067518 0.98 DRD2 (0.64) DRD2DRD3DRD1DRD4DRD5
SCHEMBL5336469 0.89 DRD2 (0.57) DRD2DRD3DRD1DRD4DRD5
SCHEMBL13993807 0.82 DRD2 (0.58) DRD2DRD3DRD1DRD4DRD5
SCHEMBL27663343 0.81 OPRK1 (0.57) DRD2DRD3DRD1DRD4DRD5
SCHEMBL3401759 0.80 OPRK1 (0.60) DRD2DRD3DRD1DRD4DRD5
SCHEMBL20683375 0.80 DRD2 (0.62) DRD2DRD3DRD1DRD4DRD5
SCHEMBL723832 0.80 DRD2 (0.74) DRD2DRD3DRD1DRD4DRD5
SCHEMBL30481367 0.80 TAAR1 (0.61) DRD2DRD3DRD1DRD4DRD5
SCHEMBL16942776 0.80 TAAR1 (0.61) DRD2DRD3DRD1DRD4DRD5
SCHEMBL11653919 0.79 DRD2 (1.00) DRD2DRD3DRD1DRD4DRD5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2011070585-A1 PROCESSES FOR PREPARING RIVASTIGMINE, SALTS AND INTERMEDIATES THEREOF SHODHANA LABORATORIES LIMITED (IN) 2011-06-16 WO claimed
EP-1856036-A1 AN EFFICIENT METHOD FOR PREPARATION OF (S)-3-[(1-DIMETHYL AMINO)ETHYL]-PHENYL-N-ETHYL-N-METHYL-CARBAMATE Emcure Pharmaceuticals Limited (IN) 2007-11-21 EP claimed
WO-2006048720-A1 AN EFFICIENT METHOD FOR PREPARATION OF (S)-3-[(1-DIMETHYL AMINO)ETHYL]-PHENYL-N-ETHYL-N-METHYL-CARBAMATE EMCURE PHARMACEUTICALS LIMITED (IN) 2006-05-11 WO claimed
WO-2003101917-A2 A PROCESS FOR THE PREPARATION OF PHENYLCARBAMATES SUN PHARMACEUTICAL INDUSTRIES LIMITED (IN) 2003-12-11 WO claimed
CN-112194767-B Benzoxazine resin containing zwitter-ion group and preparation method and application thereof 山东大学 2021-06-29 CN disclosed
CN-112142935-B Benzoxazine resin containing quaternary ammonium group and preparation method and application thereof 山东大学 2021-06-29 CN disclosed
CN-112194767-A Benzoxazine resin containing zwitter-ion group and preparation method and application thereof 山东大学 2021-01-08 CN disclosed
US-10882819-B2 Synthesis of novel intermediate(s) for preparing rivastigmine Cadila Corporate Campus (IN) 2021-01-05 US disclosed
CN-112142935-A Benzoxazine resin containing quaternary ammonium group and preparation method and application thereof 山东大学 2020-12-29 CN disclosed
US-20200095195-A1 SYNTHESIS OF NOVEL INTERMEDIATE(S) FOR PREPARING RIVASTIGMINE CADILA PHARMACEUTICALS, LTD. (IN) 2020-03-26 US disclosed
EP-2582799-B1 BIOCATALYSTS AND METHODS FOR THE SYNTHESIS OF (S)-3-(1-AMINOETHYL)-PHENOL CODEXIS INC (US) 2017-12-20 EP disclosed
US-9783500-B2 2-aminoquinoline-based compounds for potent and selective neuronal nitric oxide synthase inhibition NORTHWESTERN UNIVERSITY (US) 2017-10-10 US disclosed
EP-0951284-B1 PHENYLETHYLAMINE DERIVATIVES TEVA PHARMA (IL) 2003-10-08 EP disclosed
EP-0951284-A4 PHENYLETHYLAMINE DERIVATIVES TEVA PHARMA (IL) 2002-03-20 EP disclosed
EP-0951284-A1 PHENYLETHYLAMINE DERIVATIVES TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 1999-10-27 EP disclosed
WO-1998026775-A1 PHENYLETHYLAMINE DERIVATIVES TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 1998-06-25 WO disclosed
WO-1996002524-A1 PHENYLCARBAMATE DERIVATIVES SUITABLE TO THE USE AS ANTICHOLINESTERASE SUBSTANCES MEDIOLANUM FARMACEUTICI S.P.A. (IT) 1996-02-01 WO disclosed
EP-0150073-B1 3,4-DISUBSTITUTED-1,2,5-OXADIAZOLES HAVING HISTAMINE H2-RECEPTOR ANTAGONIST ACTIVITY Bristol-Myers Squibb Company (US) 1990-09-26 EP disclosed
EP-0150073-A1 3,4-Disubstituted-1,2,5-oxadiazoles having histamine H2-receptor antagonist activity Bristol-Myers Squibb Company (US) 1985-07-31 EP disclosed
US-4507485-A 3,4-Disubstituted-1,2,5-oxadiazoles having histamine H2 -receptor antagonist activity BRISTOL-MYERS COMPANY (US) 1985-03-26 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-10882819-B2 Synthesis of novel intermediate(s) for preparing rivastigmine ACHE, SQLE, BCHE DRD2 677/4885DRD3 917/4885DRD1 623/4885
US-20200095195-A1 SYNTHESIS OF NOVEL INTERMEDIATE(S) FOR PREPARING RIVASTIGMINE ACHE, SQLE, BCHE DRD2 677/4885DRD3 917/4885DRD1 623/4885

“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.