Orphenadrine

Orphenadrine

SCHEMBL1235378

Cc1ccccc1C(OCCN(C)C)c1ccccc1.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHRH1SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASLC6A2

The experimentally established mechanism targets of Orphenadrine. 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 0.97
HRH1 known ✓ P35367 3/20 0.97
GRIN2D known ✓ O15399 1/20 0.97
GRIN3B known ✓ O60391 1/20 0.97
GRIN1 known ✓ Q05586 1/20 0.97
GRIN2A known ✓ Q12879 1/20 0.97
GRIN2B known ✓ Q13224 1/20 0.97
GRIN2C known ✓ Q14957 1/20 0.97
GRIN3A known ✓ Q8TCU5 1/20 0.97
SCN1A known ✓ P35498 1/20 0.71
SCN5A known ✓ Q14524 1/20 0.71
SCN2A known ✓ Q99250 1/20 0.71
SCN3A known ✓ Q9NY46 1/20 0.71
LMNA P02545 5/20 1.00
PMP22 Q01453 2/20 1.00
BLM P54132 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00
SLC6A4 P31645 6/20 0.97
SLC6A3 Q01959 6/20 0.97
CYP2D6 P10635 4/20 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
Orphenadrine SCHEMBL30903909 1.00 LMNA (1.00) LMNAPMP22BLMNPSR1SLC6A2
Orphenadrine SCHEMBL119471 0.98 SLC6A2 (1.00) LMNAPMP22BLMNPSR1SLC6A2
Orphenadrine SCHEMBL29359844 0.98 SLC6A2 (1.00) LMNAPMP22BLMNPSR1SLC6A2
Orphenadrine SCHEMBL28727 0.98 SLC6A2 (1.00) LMNAPMP22BLMNPSR1SLC6A2
Orphenadrine SCHEMBL4338150 0.95 SLC6A2 (0.94) LMNAPMP22BLMNPSR1SLC6A2
Hydrochloric Acid SCHEMBL29519368 0.91 LMNA (0.84) LMNAPMP22BLMNPSR1SLC6A2
Hydrochloric Acid SCHEMBL29519484 0.88 LMNA (0.78) LMNAPMP22BLMNPSR1SLC6A2
SCHEMBL2615259 0.87 SLC6A2 (0.79) LMNAPMP22BLMNPSR1SLC6A2
SCHEMBL637495 0.87 SLC6A2 (0.78) LMNAPMP22BLMNPSR1SLC6A2
Diphenhydramine SCHEMBL17071 0.85 LMNA (1.00) LMNAPMP22BLMNPSR1SLC6A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4724114-A1 CYANOACRYLATE ADHESIVE KITS Chemence, Inc. (US) 2026-04-15 EP claimed
WO-2026041855-A1 CYANOACRYLATE ADHESIVE KITS CHEMENCE, INC. (US) 2026-02-26 WO claimed
US-20200131431-A1 CHEMICAL ADDITIVES AND SURFACTANT COMBINATIONS FOR FAVORABLE WETTABILITY ALTERATION AND IMPROVED HYDROCARBON RECOVERY FACTORS ALCHEMY SCIENCES INC (US) 2020-04-30 US claimed
US-20190133924-A1 Alcohol-Resistant Formulations CIMA LABS INC (US) 2019-05-09 US claimed
US-10154856-B2 Therapeutic substance transfer catheter and method SILLENDER MARK (AU) 2018-12-18 US claimed
US-9757376-B2 Pharmaceutical compositions GM PHARMACEUTICALS, INC. (US) 2017-09-12 US claimed
US-20150359566-A1 THERAPEUTIC SUBSTANCE TRANSFER CATHETER AND METHOD SILLENDER MARK (US) 2015-12-17 US claimed
EP-2953678-A1 THERAPEUTIC SUBSTANCE TRANSFER CATHETER AND METHOD Sillender, Mark (AU) 2015-12-16 EP claimed
WO-2014121332-A1 THERAPEUTIC SUBSTANCE TRANSFER CATHETER AND METHOD SILLENDER MARK (AU) 2014-08-14 WO claimed
US-20040259809-A1 Pharmaceutical compositions including an antihistamine and a stimulant and method of use thereof PEDIAMED PHARMACEUTICALS, INC. 2004-12-23 US claimed
EP-1476195-A2 ENHANCEMENT OF THE ACTION OF CENTRAL AND PERIPHERAL NERVOUS SYSTEM AGENTS PITMY INTERNATIONAL N.V. (AN) 2004-11-17 EP claimed
WO-2002005851-A2 ENHANCEMENT OF THE ACTION OF CENTRAL AND PERIPHERAL NERVOUS SYSTEM AGENTS PITMY INTERNATIONAL N.V. (AN) 2002-01-24 WO claimed
US-5045454-A Iron chelate, aurintricarboxylic acid, and chelate compounds MEDI-CULT A/S (DK) 1991-09-03 US claimed
US-4244941-A POROUS COATING OF COMPRESSED POWDERS ALLOWS CONSTANT RELEASE OF CORE SUBSTANCE GIST-BROCADES N.V. (NL) 1981-01-13 US claimed
EP-4724114-A1 CYANOACRYLATE ADHESIVE KITS Chemence, Inc. (US) 2026-04-15 EP disclosed
WO-2026041855-A1 CYANOACRYLATE ADHESIVE KITS CHEMENCE, INC. (US) 2026-02-26 WO disclosed
US-20260014136-A1 LIPOPHILIC ACTIVE ORAL FILM FORMULATION AND METHOD OF MAKING THE SAME INTELGENX CORP (CA) 2026-01-15 US disclosed
EP-0055043-A2 6,7,8,9-Tetrahydro-3H-benz(e)indolamine derivatives, processes for their preparation and intermediates used therein, and pharmaceutical compositions containing the indolamine derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1982-06-30 EP disclosed
EP-0034894-A2 2-(1-Piperazinyl)-2,4,6-cycloheptatrien-1-one derivatives, processes for their preparation, intermediates used in the processes and the preparation thereof and pharmaceutical compositions containing the derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1981-09-02 EP disclosed
US-4244941-A POROUS COATING OF COMPRESSED POWDERS ALLOWS CONSTANT RELEASE OF CORE SUBSTANCE GIST-BROCADES N.V. (NL) 1981-01-13 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 (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-20260014136-A1 LIPOPHILIC ACTIVE ORAL FILM FORMULATION AND METHOD OF MAKING THE SAME MGLL, NPC1L1, LIPA SLC6A2 1076/4885HRH1 1219/4885GRIN2D 3039/4885

“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.