Milnacipran

Milnacipran

SCHEMBL114034

CCN(CC)C(=O)C1(c2ccccc2)CC1CN

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2SLC6A4

The experimentally established mechanism targets of Milnacipran. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 13/20 1.00
SLC6A4 known ✓ P31645 12/20 1.00
SLC6A3 Q01959 5/20 1.00
CYP2D6 P10635 1/20 1.00
HTR2C P28335 1/20 1.00
KDM4E B2RXH2 1/20 0.97
MAPK1 P28482 1/20 0.97

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
1R,2S-Milnacipran SCHEMBL30083111 1.00 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Levomilnacipran SCHEMBL12027608 1.00 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Levomilnacipran SCHEMBL1707471 1.00 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
1R,2S-Milnacipran SCHEMBL5504533 1.00 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Levomilnacipran SCHEMBL1414867 1.00 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
1R,2S-Milnacipran SCHEMBL8099 1.00 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Milnacipran SCHEMBL1156056 0.99 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
1R,2S-Milnacipran SCHEMBL4434769 0.99 SLC6A2 (1.00) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
1R,2S-Milnacipran SCHEMBL16241424 0.99 SLC6A2 (0.97) SLC6A2SLC6A4SLC6A3CYP2D6HTR2C
Levomilnacipran SCHEMBL1289763 0.99 SLC6A2 (1.00) 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 484 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111362824-B Process for the preparation of 2- (aminomethyl) -N, N-diethyl-1-phenylcyclopropanecarboxamide and salts thereof 四川科瑞德制药股份有限公司 2023-03-24 CN claimed
US-11497739-B2 Materials and methods for diagnosis, prevention and/or treatment of stress disorders and conditions associated with a-beta peptide aggregation UNIVERSITY OF SOUTH FLORIDA (US) 2022-11-15 US claimed
WO-2014203277-A2 PROCESS FOR THE PREPARATION OF (1S,2R)-2-(AMINOMETHYL)-N,N-DIETHYL-1-PHENYLCYCLOPROPANEARBOXAMIDE HYDROCHLORIDE MSN LABORATORIES PRIVATE LIMITED (IN) 2014-12-24 WO claimed
US-20130253063-A1 STABLE DOSAGE FORMS OF LEVOMILNACIPRAN FOREST LABORATORIES HOLDINGS LTD. (BM) 2013-09-26 US 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
EP-1908461-B9 Use of (1S, 2R) enantiomer of milnacipran for the preparation of a medicine PF MEDICAMENT (FR) 2011-08-31 EP claimed
EP-1770084-B1 METHOD FOR PRODUCING (Z)-1-PHENYL-1-DIETHYLAMINOCARBONYL-2-AMINOMETHYL CYCLOPROPANE HYDROCHLORIDE SUMITOMO CHEMICAL CO (JP) 2011-08-24 EP 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
EP-1908461-B1 Use of (1S, 2R) enantiomer of milnacipran for the preparation of a medicine PF MEDICAMENT (FR) 2011-03-16 EP claimed
EP-1770084-A1 METHOD FOR PRODUCING (Z)-1-PHENYL-1-DIETHYLAMINOCARBONYL-2-AMINOMETHYL CYCLOPROPANE HYDROCHLORIDE Sumitomo Chemical Company, Limited (JP) 2007-04-04 EP claimed
US-7074833-B2 Use of the (1S,2R) enantiomer of milnacipran for the preparation of a drug PIERRE FABRE MEDICAMENT (FR) 2006-07-11 US claimed
US-20060014837-A1 Use of the (1S, 2R) enantiomer of milnacipran for the preparation of a drug PIERRE FABRE MEDICAMENT (FR) 2006-01-19 US claimed
EP-1601349-A1 USE OF THE ENANTIOMER (1S, 2R) OF MILNACIPRAN FOR THE PREPARATION OF A MEDICAMENT PIERRE FABRE MEDICAMENT (FR) 2005-12-07 EP claimed
US-20040259953-A1 Use of the (1S,2R) enantiomer of milnacipran for the preparation of a drug PIERRE FABRE MEDICAMENT (FR) 2004-12-23 US claimed
WO-2004075886-A1 USE OF THE ENANTIOMER (1S, 2R) OF MILNACIPRAN FOR THE PREPARATION OF A MEDICAMENT PIERRE FABRE MEDICAMENT (FR) 2004-09-10 WO claimed
US-20040162334-A1 Use of the dextrogyral enantiomer of milnacipran for the preparation of a drug PIERRE FABRE MEDICAMENT (FR) 2004-08-19 US claimed
EP-0200638-B1 PROCESS FOR THE PREPARATION OF (Z)-1-PHENYL-1-DIETHYL AMINO CARBONYL 2-AMINO METHYL CYCLOPROPANE HYDROCHLORIDE PIERRE FABRE MEDICAMENT (FR) 1989-04-19 EP claimed
EP-0068999-B1 DERIVATIVES OF 1-ARYL-2-AMINOMETHYL-CYCLOPROPANE-CARBOXAMIDES (Z), THEIR PREPARATION AND THEIR USE AS MEDICINES IN THE TREATMENT OF DISORDERS OF THE CENTRAL NERVOUS SYSTEM PIERRE FABRE S.A. (FR) 1985-05-22 EP claimed
US-4478836-A 1-Aryl 2-aminomethyl cyclopropane carboxyamide (Z) derivatives and their use as useful drugs in the treatment of disturbances of the central nervous system PIERRE FABRE S.A. (FR) 1984-10-23 US 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-20060014837-A1 Use of the (1S, 2R) enantiomer of milnacipran for the preparation of a drug SLC6A2, ADRA1D, HTR3A SLC6A2 1/4885SLC6A4 8/4885SLC6A3 20/4885
US-11497739-B2 Materials and methods for diagnosis, prevention and/or treatment of stress disorders and conditions associated with a-beta peptide aggregation APP, BACE1, BDNF SLC6A2 39/4885SLC6A4 115/4885SLC6A3 35/4885
US-20040259953-A1 Use of the (1S,2R) enantiomer of milnacipran for the preparation of a drug SLC6A2, ADRA1D, HTR3A SLC6A2 1/4885SLC6A4 8/4885SLC6A3 20/4885
US-20130253063-A1 STABLE DOSAGE FORMS OF LEVOMILNACIPRAN LPXN, TNNC1, TNNI3 SLC6A2 33/4885SLC6A4 4/4885SLC6A3 91/4885
US-20040162334-A1 Use of the dextrogyral enantiomer of milnacipran for the preparation of a drug SLC6A4, SLC6A2, HTR6 SLC6A2 2/4885SLC6A4 1/4885SLC6A3 9/4885

“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.