Citalopram

Citalopram

SCHEMBL946

CN(C)CCCC1(c2ccc(F)cc2)OCc2cc(C#N)ccc21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A4

The experimentally established mechanism targets of Citalopram. 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
SLC6A4 known ✓ P31645 14/20 1.00
SLC6A2 P23975 2/20 1.00
HTR2C P28335 2/20 1.00
ADRA1A P35348 2/20 1.00
HRH1 P35367 2/20 1.00
OPRM1 P35372 2/20 1.00
DRD3 P35462 2/20 1.00
HTR2B P41595 2/20 1.00
KCNH2 Q12809 2/20 1.00
NPC1 O15118 1/20 1.00
SLC22A1 O15245 1/20 1.00
ALDH1A1 P00352 1/20 1.00
CHRM2 P08172 1/20 1.00
HTR1A P08908 1/20 1.00
CHRM1 P11229 1/20 1.00
DRD1 P21728 1/20 1.00
ACHE P22303 1/20 1.00
HRH2 P25021 1/20 1.00
ADRA1D P25100 1/20 1.00
HTR2A P28223 1/20 1.00

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
(R)-Citalopram SCHEMBL13235283 1.00 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Citalopram SCHEMBL29494157 1.00 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
(R)-Citalopram SCHEMBL29414626 1.00 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Escitalopram SCHEMBL29358316 1.00 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Citalopram SCHEMBL3858802 1.00 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Escitalopram SCHEMBL34948 1.00 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Escitalopram SCHEMBL522164 0.99 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Citalopram SCHEMBL1118 0.99 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1
Citalopram SCHEMBL21820669 0.99 SLC6A4 (0.98) SLC6A4SLC6A2HTR2CADRA1AHRH1
Citalopram SCHEMBL1286979 0.99 SLC6A4 (1.00) SLC6A4SLC6A2HTR2CADRA1AHRH1

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 38366 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3607938-B1 PHARMACEUTICAL COMPOSITION SOVIC BRKICIC LJILJANA (HR) 2026-05-27 EP claimed
EP-4746863-A1 ENDOXIFEN COMPOSITIONS AND METHODS OF USE THEREOF AND SYNTHESIS THEREOF Atossa Therapeutics, Inc. (US) 2026-05-27 EP claimed
CN-122079853-A N-substituted indoles and other heterocyclic compounds for the treatment of brain diseases 2026-05-26 CN claimed
CN-122094963-A Cardioprotective lipids and methods of use 2026-05-26 CN claimed
CN-110609095-B Method for determining citalopram or a salt thereof and related substances in a formulation thereof 苏州科伦药物研究有限公司 2026-05-15 CN claimed
US-20260131089-A1 DRUG DELIVERY DEVICES AND METHODS FOR ADMINISTERING SUBSTANCES TO A BODY CAVITY BY HETEROGENOUS AEROSOLIZATION FOR TREATMENT OF BINGE-EATING DISORDERS AND/OR OBESITY APTARGROUP, INC. (US) 2026-05-14 US claimed
EP-4739303-A2 MDMA ENANTIOMER COMPOSITIONS AND METHODS FOR MODULATING AGGRESSION RESPONSE EmpathBio, Inc. (US) 2026-05-13 EP claimed
US-12624036-B2 Method of treating post-traumatic stress disorder INTRA-CELLULAR THERAPIES, INC. (US) 2026-05-12 US claimed
US-12624037-B2 Method of treating agitation, aggressive behavior, and impulse control disorder INTRA-CELLULAR THERAPIES, INC. (US) 2026-05-12 US claimed
US-12617809-B2 Cardioprotective lipid and method of use SIGNPATH PHARMA, INC. (US) 2026-05-05 US claimed
WO-1990004387-A2 COMPOSITIONS FOR TREATING TOBACCO WITHDRAWAL SYMPTOMS MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1990-05-03 WO claimed
EP-0347066-A1 New enantiomers and their isolation H. LUNDBECK A/S (DK) 1989-12-20 EP claimed
WO-1989003692-A1 TREATING PREMENSTRUAL OR LATE LUTEAL PHASE SYNDROME MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1989-05-05 WO claimed
EP-0303961-A2 Novel antidepressants MERRELL DOW PHARMACEUTICALS INC. (US) 1989-02-22 EP claimed
EP-0293714-A1 Combinations of compounds with anti-depressive activity Troponwerke GmbH & Co. KG (DE) 1988-12-07 EP claimed
EP-0171943-B1 NOVEL INTERMEDIATE AND METHOD FOR ITS PREPARATION H. LUNDBECK A/S (DK) 1988-11-17 EP claimed
US-4650884-A 4-[4-(dimethylamino)-1-(4'-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)-benzonitrile (racemic citalopram diol) as intermediate to citalopram H. LUNDBECK A/S (DK) 1987-03-17 US claimed
EP-0171943-A1 Novel intermediate and method for its preparation H. LUNDBECK A/S (DK) 1986-02-19 EP claimed
EP-0152379-A2 Process for preparing pharmaceutical compositions containing unilamellar liposomes CIBA-GEIGY AG (CH) 1985-08-21 EP claimed
US-4136193-A ANTI-DEPRESSIVE SUBSTITUTED 1-DIMETHYLAMINOPROPYL-1-PHENYL PHTHALANS KEFALAS A/S (DK) 1979-01-23 US claimed