Desipramine

Desipramine

SCHEMBL41993

CNCCCN1c2ccccc2CCc2ccccc21.[Cl-].[H+]

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 6/20 0.94
SLC6A4 P31645 8/20 0.94
CYP3A4 P08684 4/20 0.94
HTR2A P28223 4/20 0.94
CHRM2 P08172 4/20 0.94
CHRM1 P11229 4/20 0.94
DRD2 P14416 4/20 0.94
CHRM3 P20309 4/20 0.94
HRH1 P35367 4/20 0.94
DRD3 P35462 4/20 0.94
SLC22A1 O15245 3/20 0.94
CYP2D6 P10635 3/20 0.94
ADRA2B P18089 3/20 0.94
ADRA2C P18825 3/20 0.94
HTR2C P28335 3/20 0.94
ADRA1A P35348 3/20 0.94
OPRK1 P41145 3/20 0.94
HTR2B P41595 3/20 0.94
MTOR P42345 3/20 0.94
CACNA1B Q00975 3/20 0.94

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
Desipramine SCHEMBL29379525 0.97 SLC6A4 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL34384 0.97 SLC6A4 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL5072939 0.97 SLC6A4 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL41992 0.95 SLC6A2 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL2944786 0.95 SLC6A2 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL29364790 0.95 SLC6A2 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL5501781 0.95 SLC6A2 (1.00) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL29085912 0.95 SLC6A4 (0.97) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL27517227 0.88 SLC6A4 (0.83) SLC6A4SLC6A2CYP3A4HTR2ACHRM2
Desipramine SCHEMBL28105338 0.88 SLC6A4 (0.83) SLC6A4SLC6A2CYP3A4HTR2ACHRM2

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

Appears in 2291 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250387343-A1 Nanoparticle Compositions and Methods for Synthesis Thereof ICEUTICA PTY LTD (AU) 2025-12-25 US claimed
WO-2025087695-A1 METHOD FOR PRODUCING RECOMBINANT ADENO-ASSOCIATED VIRUS PARTICLES ASCEND ADVANCED THERAPIES LTD (GB) 2025-05-01 WO claimed
US-20240122855-A1 Methods for the preparation of biologically active compounds in nanoparticulate form ICEUTICA PTY LTD. (AU) 2024-04-18 US claimed
US-20240016814-A1 METHOD OF TREATING HYPERTENSION CIPLA LIMITED (IN) 2024-01-18 US claimed
US-20220054418-A1 Methods for the preparation of biologically active compounds in nanoparticulate form ICEUTICA PTY LTD. (AU) 2022-02-24 US claimed
US-11033572-B2 Molecular adjuvants for enhanced cytosolic delivery of active agents UNIVERSITEIT GENT (BE) 2021-06-15 US claimed
US-20200405729-A1 METHOD OF TREATING HYPERTENSION CIPLA LIMITED (IN) 2020-12-31 US claimed
US-20200360294-A1 Nanoparticle Compositions and Methods for Synthesis Thereof ICEUTICA PTY LTD. (AU) 2020-11-19 US claimed
EP-2054042-B1 METHODS FOR THE PREPARATION OF BIOLOGICALLY ACTIVE COMPOUNDS IN NANOPARTICULATE FORM ICEUTICA PTY LTD (AU) 2020-04-29 EP claimed
US-20190328768-A1 MOLECULAR ADJUVANTS FOR ENHANCED CYTOSOLIC DELIVERY OF ACTIVE AGENTS UNIVERSITEIT GENT (BE) 2019-10-31 US claimed
US-20030139698-A1 Medicated wrap HYSON MORTON I (US) 2003-07-24 US claimed
EP-1309301-A1 MEDICATED WRAP Hyson, Morton I. (US) 2003-05-14 EP claimed
EP-1273301-A2 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON S.A. (CH) 2003-01-08 EP claimed
US-20020035105-A1 Composition and method combining an antidepressant with an NMDA receptor antagonist, for treating neuropathic pain ENDO PHARMACEUTICALS INC. 2002-03-21 US claimed
WO-2001080797-A1 MEDICATED WRAP HYSON MORTON I (US) 2001-11-01 WO claimed
EP-0980247-A1 COMPOSITION AND METHOD COMBINING AN ANTIDEPRESSANT WITH AN NMDA RECEPTOR ANTAGONIST, FOR TREATING NEUROPATHIC PAIN Algos Pharmaceutical Corporation (US) 2000-02-23 EP claimed
WO-1998050044-A1 COMPOSITION AND METHOD COMBINING AN ANTIDEPRESSANT WITH AN NMDA RECEPTOR ANTAGONIST, FOR TREATING NEUROPATHIC PAIN ALGOS PHARMACEUTICAL CORPORATION (US) 1998-11-12 WO claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
EP-0741570-A1 METHOD FOR PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO MEDICATIONS G.D. SEARLE & CO. (US) 1996-11-13 EP claimed
WO-1995020387-A1 METHOD FOR PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO MEDICATIONS G.D. SEARLE & CO. (US) 1995-08-03 WO claimed