Amantadine

Amantadine

SCHEMBL321979

NC12CC3CC(CC(C3)C1)C2.O=S(=O)(O)O

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BM

The experimentally established mechanism targets of Amantadine. 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
GRIN2D known ✓ O15399 3/20 0.68
GRIN3B known ✓ O60391 3/20 0.68
GRIN1 known ✓ Q05586 3/20 0.68
GRIN2A known ✓ Q12879 3/20 0.68
GRIN2B known ✓ Q13224 3/20 0.68
GRIN2C known ✓ Q14957 3/20 0.68
GRIN3A known ✓ Q8TCU5 3/20 0.68
LMNA P02545 3/20 0.68
SLC22A1 O15245 2/20 0.68
NFKB1 P19838 2/20 0.68
TSHR P16473 2/20 0.68
SLC22A2 O15244 1/20 0.68
STAT6 P42226 1/20 0.68
SLC47A1 Q96FL8 1/20 0.68
SIGMAR1 Q99720 1/20 0.68
THRB P10828 2/20 0.65
POLB P06746 2/20 0.65
BLM P54132 1/20 0.65
PMP22 Q01453 1/20 0.65
SMN1; SMN2 Q16637 1/20 0.65

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
Amantadine SCHEMBL5919747 1.00 LMNA (0.68) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL1073029 1.00 LMNA (0.68) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL29011286 0.83 GRIN1 (0.87) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL21309814 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL15532073 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL3642447 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL4098 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL21310017 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL15672299 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A
Amantadine SCHEMBL20409394 0.83 GRIN1 (1.00) LMNAGRIN2DGRIN3BGRIN1GRIN2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119661366-A Preparation method and application of amantadine carbonate 李果 2025-03-21 CN claimed
CN-117843492-A Method for separating and extracting product in production of amantadine 四川众邦新材料股份有限公司 2024-04-09 CN claimed
CN-112010764-A Preparation method of 3-hydroxy-1-amantadine transition state intermediate 江苏泰洁智邦检测技术有限公司 2020-12-01 CN claimed
CN-107325010-A The safe preparation method and device of a kind of adamantanol 四川众邦制药有限公司 2017-11-07 CN claimed
CN-102883601-A amantadine compositions and methods of use thereof ADAMAS PHARMACEUTICALS INC 2013-01-16 CN claimed
EP-2506709-A2 AMANTADINE COMPOSITIONS AND METHODS OF USE Adamas Pharmaceuticals, Inc. (US) 2012-10-10 EP claimed
WO-2011069010-A2 AMANTADINE COMPOSITIONS AND METHODS OF USE ADAMAS PHARMACEUTICALS, INC. (US) 2011-06-09 WO claimed
EP-1562860-B1 METHOD FOR PRODUCING ALKALINE EARTH SULPHATE NANOPARTICLES CT FUER ANGEWANDTE NANOTECHNOLOGIE CAN GMBH (DE) 2011-04-27 EP claimed
US-7288239-B2 Having a crystal lattice of Mg, Ca, Sr and/or Ba sulfate obtained by controlled crystal growth in a non-aqueous solvent such as glycerin, ethylene glycol, polyethylene glycols, polyalcohols or dimethyl sulfoxide with coordinating properties NANOSOLUTIONS GMBH (DE) 2007-10-30 US claimed
US-20060133987-A1 Having a crystal lattice of Mg, Ca, Sr and/or Ba sulfate obtained by controlled crystal growth in a non-aqueous solvent such as glycerin, ethylene glycol, polyethylene glycols, polyalcohols or dimethyl sulfoxide with coordinating properties CENTRUM FUR ANGEWANDTE NANOTECHNOLOGIE (CAN) GMBH (DE) 2006-06-22 US claimed
EP-0935461-B1 ADAMANTANE AMINE DERIVATIVES FOR THE TREATMENT OF VIRUSES OF THE BORNAVIRIDAE FAMILY LUDWIG HANNS (DE) 2003-07-30 EP claimed
US-6384083-B1 CONTROLLING VIRUSES OF BORNAVIRIDAE FAMILY BY ADMINISTERING ADAMANTANE AMINES TO HUMAN AND ANIMALS AT THERAPEUTICALLY EFFECTIVE DOSAGE BY MEANS SELECTED FROM ORAL, PARENTERAL, INTRAMUSCULAR, SUBCUTANEOUS, INTRADERMAL AND TOPICAL Ludwig, Hanns (DE) 2002-05-07 US claimed
CN-1235540-A Use of amantadine or structurally similar compounds for combating borna disease virus and preventing and treating affective disorders and other diseases associated with BDV infection in humans and animals LUDWIG H (DE) 1999-11-17 CN claimed
EP-4719353-A1 REVERSIBLE SURFACTANT AND MULTIFUNCTIONAL DRUG DELIVERY SYSTEMS BASED THEREON Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. (IL) 2026-04-08 EP disclosed
US-20260091073-A1 COMPOSITIONS CONTAINING SILYMARIN AND SULFOALKYL ETHER CYCLODEXTRIN AND METHODS OF USING THE SAME CYDEX PHARMACEUTICALS INC (US) 2026-04-02 US disclosed
EP-4620534-A2 COMPOSITIONS CONTAINING SILYMARIN AND SULFOALKYL ETHER CYCLODEXTRIN AND METHODS OF USING THE SAME CyDex Pharmaceuticals, Inc. (US) 2025-09-24 EP disclosed
EP-0351897-A2 Skin penetration system for salts of amine-functional drugs THE PROCTER & GAMBLE COMPANY (US) 1990-01-24 EP disclosed
EP-0139504-B1 ADAMANTYLAMINE/LONG CHAIN ALKYLAMINE CATALYSTS AND USE IN PARAFFIN-OLEFIN ALKYLATION PROCESS EXXON RESEARCH AND ENGINEERING COMPANY (US) 1988-06-08 EP disclosed
US-4560825-A CHARGE TRANSFER, LEWIS ACIDS, ADAMANTANYLAMINE AND DODECYLAMINE; ANTIKNOCK COMPOUNDS EXXON RESEARCH & ENGINEERING COMPANY (US) 1985-12-24 US disclosed
EP-0139504-A1 Adamantylamine/long chain alkylamine catalysts and use in paraffin-olefin alkylation process EXXON RESEARCH AND ENGINEERING COMPANY (US) 1985-05-02 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-20260091073-A1 COMPOSITIONS CONTAINING SILYMARIN AND SULFOALKYL ETHER CYCLODEXTRIN AND METHODS OF USING THE SAME GYS2, COL1A1, COL14A1 GRIN2D 4810/4885GRIN3B 4720/4885GRIN1 4852/4885

“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.