Ladostigil

Ladostigil

SCHEMBL2387320

C#CCN[C@@H]1CCc2ccc(OC(=O)N(C)CC)cc21.C#CCN[C@@H]1CCc2ccc(OC(=O)N(C)CC)cc21.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.87

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
ACHE P22303 19/20 0.87
MAOA P21397 2/20 0.87
MAOB P27338 2/20 0.87
BCHE P06276 1/20 0.87

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
Ladostigil SCHEMBL30579760 1.00 ACHE (0.87) ACHEMAOAMAOBBCHE
Ladostigil SCHEMBL3893996 0.93 ACHE (1.00) ACHEMAOAMAOBBCHE
Ladostigil SCHEMBL678895 0.93 ACHE (1.00) ACHEMAOAMAOBBCHE
Ladostigil SCHEMBL3301711 0.93 ACHE (1.00) ACHEMAOAMAOBBCHE
SCHEMBL13853627 0.88 ACHE (1.00) ACHEMAOAMAOBBCHE
SCHEMBL13853626 0.85 ACHE (0.84) ACHEMAOAMAOBBCHE
SCHEMBL12043626 0.85 ACHE (0.84) ACHEMAOAMAOBBCHE
SCHEMBL3895981 0.84 ACHE (0.98) ACHEMAOAMAOBBCHE
SCHEMBL13449663 0.84 ACHE (0.98) ACHEMAOAMAOBBCHE
SCHEMBL3895985 0.84 ACHE (0.98) ACHEMAOAMAOBBCHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4719474-A1 METHOD OF TREATING FIBROTIC-RELATED CONDITION Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. (IL) 2026-04-08 EP disclosed
US-20260048083-A1 METHOD OF TREATING ALZHEIMER'S DISEASE WITH EXPANDED NATURAL KILLER CELLS NKMAX CO LTD (KR) 2026-02-19 US disclosed
EP-3782649-B1 BIODEGRADABLE POLYETHYLENE GLYCOL BASED WATER-INSOLUBLE HYDROGELS ASCENDIS PHARMA AS (DK) 2025-05-14 EP disclosed
WO-2024252394-A1 METHOD OF TREATING FIBROTIC-RELATED CONDITION YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. (IL) 2024-12-12 WO disclosed
WO-2024238387-A1 METHOD OF TREATING ALZHEIMER'S DISEASE WITH EXPANDED NATURAL KILLER CELLS NKMAX CO., LTD. (KR) 2024-11-21 WO disclosed
US-20240074995-A1 METHODS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH AN ABNORMAL INFLAMMATORY RESPONSES FIRST WAVE BIO, INC. 2024-03-07 US disclosed
WO-2024036005-A1 METHOD OF TREATING ALZHEIMER'S DISEASE WITH EXPANDED NATURAL KILLER CELLS NKMAX CO., LTD. (KR) 2024-02-15 WO disclosed
US-20230384333-A1 GPCR SCREENING METHOD TO IDENTIFY NON-HALLUCINOGENIC COMPOUNDS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2023-11-30 US disclosed
US-20230381323-A1 RELEASABLE CONJUGATES FISH & RICHARDSON PC 2023-11-30 US disclosed
US-20230357154-A1 BUTYRYLCHOLINESTERASE COMPOUNDS AND USE IN DISEASES OF THE NERVOUS SYSTEM TREVENTIS CORPORATION (US) 2023-11-09 US disclosed
US-20070203232-A1 Propargylated aminoindans, processes for preparation, and uses thereof TECHNION RESEARCH AND DEVELOPMENT FOUNDATION LTD. (IL) 2007-08-30 US disclosed
WO-2007061717-A2 METHODS FOR ISOLATING PROPARGYLATED AMINOINDANS TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2007-05-31 WO disclosed
US-20070112217-A1 Methods for isolating propargylated aminoindans TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2007-05-17 US disclosed
WO-2006120577-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF ENANTIOMERIC INDANYLAMINE DERIVATIVES TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-11-16 WO disclosed
WO-2006091836-A9 FORMULATIONS OF LADOSTIGIL TARTRATE TEVA PHARMA (IL) 2006-10-26 WO disclosed
US-20060199974-A1 propynylaminoindans including alkoxy or alkylcarbamates derivatives, prepared by reduction of indanones in the presence of hydrogenation catalysts to form indanols and reacting the indanols with propargylamine under nucleophilic substitution to form drugs for the treatment of nervous system disorders TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-09-07 US disclosed
WO-2006091656-A1 CRYSTALS OF LADOSTIGIL TARTRATE, METHODS OF PRODUCTION AND PHARMACEUTICAL COMPOSITIONS THEREOF TEVA PHARMACEUTICAL INDUSTRIES, LTD (IL) 2006-08-31 WO disclosed
WO-2006091836-A1 FORMULATIONS OF LADOSTIGIL TARTRATE TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2006-08-31 WO disclosed
US-20060189685-A1 Formulations of ladostigil tartrate TECHNION RESEARCH AND DEVELOPMENT FOUNDATION LTD. (40%) (IL) 2006-08-24 US disclosed
US-20060189819-A1 Crystals of ladostigil tartrate, methods of production and pharmaceutical compositions thereof TEVA PHARMACEUTICAL INDUSTRIES, LTD. 2006-08-24 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 (10 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-20240074995-A1 METHODS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH AN ABNORMAL INFLAMMATORY RESPONSES FH, CS, ECHS1 ACHE 1641/4885MAOA 2331/4885MAOB 2721/4885
US-20060189819-A1 Crystals of ladostigil tartrate, methods of production and pharmaceutical compositions thereof LIPA, MTTP, LPXN ACHE 143/4885MAOA 2360/4885MAOB 3315/4885
US-20070112217-A1 Methods for isolating propargylated aminoindans AAAS, AGT, ARL1 ACHE 1083/4885MAOA 1000/4885MAOB 1418/4885
US-20230357154-A1 BUTYRYLCHOLINESTERASE COMPOUNDS AND USE IN DISEASES OF THE NERVOUS SYSTEM BCHE, ACHE, CHAT ACHE 2/4885MAOA 14/4885MAOB 8/4885
US-20060199974-A1 propynylaminoindans including alkoxy or alkylcarbamates derivatives, prepared by reduction of indanones in the presence of hydrogenation catalysts to form indanols and reacting the indanols with propargylamine under nucleophilic substitution to form drugs for the treatment of nervous system disorders ICMT, INMT, PNMT ACHE 23/4885MAOA 537/4885MAOB 407/4885
US-20230381323-A1 RELEASABLE CONJUGATES GUSB, ABCB11, UGT2B7 ACHE 403/4885MAOA 164/4885MAOB 23/4885
US-20060189685-A1 Formulations of ladostigil tartrate LIPG, LIPA, LPL ACHE 62/4885MAOA 2616/4885MAOB 2753/4885
US-20260048083-A1 METHOD OF TREATING ALZHEIMER'S DISEASE WITH EXPANDED NATURAL KILLER CELLS IL2, PBK, IL2RA ACHE 99/4885MAOA 1708/4885MAOB 1581/4885
US-20070203232-A1 Propargylated aminoindans, processes for preparation, and uses thereof PRMT3, PRMT1, PNMT ACHE 76/4885MAOA 511/4885MAOB 510/4885
US-20230384333-A1 GPCR SCREENING METHOD TO IDENTIFY NON-HALLUCINOGENIC COMPOUNDS HTR4, HTR6, HTR1A ACHE 649/4885MAOA 216/4885MAOB 218/4885

“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.