SCHEMBL1289614

SCHEMBL1289614

CCN(CC)C(=O)C1(c2ccccc2)CC1CO

nearest known ligand 0.77

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
SLC6A2 P23975 14/20 0.77
SLC6A4 P31645 11/20 0.77
SLC6A3 Q01959 4/20 0.77
CYP2D6 P10635 1/20 0.77
HTR2C P28335 1/20 0.77
KDM4E B2RXH2 1/20 0.75
MAPK1 P28482 1/20 0.75

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
SCHEMBL9993370 1.00 SLC6A2 (0.77) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL15433960 1.00 SLC6A2 (0.77) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL12067203 1.00 SLC6A2 (0.77) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL10358548 0.90 SLC6A2 (0.79) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL16501556 0.90 SLC6A2 (0.79) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL14325977 0.90 SLC6A2 (0.79) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL9994530 0.87 SLC6A2 (0.75) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Levomilnacipran SCHEMBL1707471 0.87 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Levomilnacipran SCHEMBL1414867 0.87 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
SCHEMBL1289654 0.87 SLC6A2 (0.75) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014009767-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF 1-ARYL 2-AMINOMETHYL CYCLOPROPANE CARBOXYAMIDE (Z) DERIVATIVES, THEIR ISOMERS AND SALTS MICRO LABS LIMITED (IN) 2014-01-16 WO claimed
EP-1767522-B1 METHOD FOR PRODUCING (Z)-1-PHENYL-1-DIETHYLAMINOCARBONYL-2-HYDROXYMETHYL CYCLOPROPANE SUMITOMO CHEMICAL CO (JP) 2013-01-16 EP claimed
WO-2012046247-A2 PROCESS FOR THE PREPARATION OF (±M1R(S), 2SRR)L-2-(AMINOMETHYL)-N,N-DIETHYL-L-PHENYLCYCLOPROPANE CARBOXAMIDE HYDROCHLORIDE MSN LABORATORIES LIMITED (IN) 2012-04-12 WO claimed
WO-2011158249-A1 PROCESS FOR PREPARATION OF MILNACIPRAN INTERMEDIATE AND ITS USE IN PREPARATION OF PURE MILNACIPRAN GLENMARK GENERICS LIMITED (IN) 2011-12-22 WO claimed
US-7943785-B2 Process for producing (Z)-1-phenyl-1-(N,N-diethylaminocarbonyl)-2- phthalimidomethylcyclopropane SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-05-17 US claimed
EP-1845084-B1 PROCESS FOR PRODUCING (Z)-1-PHENYL-1-(N,N-DIETHYLAMINOCARBONYL)IDOMETHYLCYCLOPROPANE SUMITOMO CHEMICAL CO (JP) 2011-04-20 EP claimed
US-20090292127-A1 Process for Producing (Z)-1-Phenyl-1-(N,N-Diethylaminocarbonyl)-2-Phthalimidomethylcyclopropane SUMITOMO CHEMICAL COMPANY, LIMITED 2009-11-26 US claimed
US-7432396-B2 Process for producing (Z)-1-phenyl-1-diethylaminocarbonyl-2-hydroxymethylcyclopropane SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2008-10-07 US claimed
US-20070249864-A1 Process for Producing (Z)-1-Phenyl-1-Diethylaminocarbonyl-2-Hydroxymethylcyclopropane SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-10-25 US claimed
EP-1767522-A1 METHOD FOR PRODUCING (Z)-1-PHENYL-1-DIETHYLAMINOCARBONYL-2-HYDROXYMETHYL CYCLOPROPANE Sumitomo Chemical Company, Limited (JP) 2007-03-28 EP claimed
EP-0377381-B1 PROCESS FOR THE PREPARATION OF 1-PHENYL-1-DIETHYL AMINO-CARBONYL-2-PHTHALIMIDE METHYL CYCLOPROPANE Z PIERRE FABRE MEDICAMENT (FR) 1992-04-22 EP claimed
US-5034541-A Method of preparing 1-phenyl-1-diethylaminocarbonyl-2-phthalimidomethyl-cyclopropane-z PIERRE FABRE MEDICAMENT (FR) 1991-07-23 US claimed
CN-113493395-A Preparation method of milnacipran hydrochloride intermediate 北京万全德众医药生物技术有限公司 2021-10-12 CN disclosed
CN-111693614-A Separation and determination method of related substances of levomilnacipran final product 万全万特制药(厦门)有限公司 2020-09-22 CN disclosed
CN-108205043-B Detection method of levomilnacipran intermediate related substance 成都弘达药业有限公司 2020-05-19 CN disclosed
EP-2805936-A1 Process for preparing levomilnacipran HCL Cosma S.p.A. (IT) 2014-11-26 EP disclosed
WO-2006001498-A1 METHOD FOR PRODUCING (Z)-1-PHENYL-1-DIETHYLAMINOCARBONYL-2-HYDROXYMETHYL CYCLOPROPANE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-01-05 WO disclosed
US-5034541-A Method of preparing 1-phenyl-1-diethylaminocarbonyl-2-phthalimidomethyl-cyclopropane-z PIERRE FABRE MEDICAMENT (FR) 1991-07-23 US disclosed
US-5034541-A Method of preparing 1-phenyl-1-diethylaminocarbonyl-2-phthalimidomethyl-cyclopropane-z PIERRE FABRE MEDICAMENT (FR) 1991-07-23 US disclosed
EP-0377381-A1 Process for the preparation of 1-phenyl-1-diethyl amino-carbonyl-2-phthalimide methyl cyclopropane Z PIERRE FABRE MEDICAMENT (FR) 1990-07-11 EP 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 (1 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-20090292127-A1 Process for Producing (Z)-1-Phenyl-1-(N,N-Diethylaminocarbonyl)-2-Phthalimidomethylcyclopropane BPNT1, CPN1, PNN SLC6A2 2105/4885SLC6A4 2288/4885SLC6A3 1267/4885

“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.