Moxisylyte

Moxisylyte

SCHEMBL317080

CC(=O)Oc1cc(C(C)C)c(OCCN(C)C)cc1C.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2C

The experimentally established mechanism targets of Moxisylyte. 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
ADRA1D known ✓ P25100 2/20 0.97
ADRA1A known ✓ P35348 2/20 0.97
ADRA1B known ✓ P35368 2/20 0.97
ADRA2A known ✓ P08913 1/20 0.97
ADRA2B known ✓ P18089 1/20 0.97
ADRA2C known ✓ P18825 1/20 0.97
SMN1; SMN2 Q16637 3/20 1.00
BLM P54132 1/20 1.00
CYP1A2 P05177 1/20 0.97
CYP2D6 P10635 1/20 0.97
PKM P14618 1/20 0.97
HTR2C P28335 1/20 0.97
HRH1 P35367 1/20 0.97
DRD3 P35462 1/20 0.97
OPRK1 P41145 1/20 0.97
CHRNA4 P43681 1/20 0.97
HIF1A Q16665 1/20 0.97
ALDH1A1 P00352 6/20 0.55
KDM4E B2RXH2 5/20 0.55
TDP1 Q9NUW8 1/20 0.55

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
Moxisylyte SCHEMBL456546 0.99 ADRA1D (1.00) SMN1; SMN2BLMADRA1DADRA1AADRA1B
Moxisylyte SCHEMBL1649830 0.96 ADRA1D (0.95) SMN1; SMN2BLMADRA1DADRA1AADRA1B
Moxisylyte SCHEMBL6398989 0.93 ADRA1D (0.88) SMN1; SMN2BLMADRA1DADRA1AADRA1B
Iproxamine SCHEMBL120331 0.86 SMN1; SMN2 (0.76) SMN1; SMN2BLMADRA1DADRA1AADRA1B
Iproxamine SCHEMBL1815834 0.85 ADRA1D (0.76) SMN1; SMN2BLMADRA1DADRA1AADRA1B
SCHEMBL5235884 0.83 ADRA1D (0.72) SMN1; SMN2BLMADRA1DADRA1AADRA1B
SCHEMBL8924260 0.83 CYP1A2 (0.72) SMN1; SMN2BLMADRA1DADRA1AADRA1B
SCHEMBL12013918 0.83 CYP1A2 (0.72) SMN1; SMN2BLMADRA1DADRA1AADRA1B
SCHEMBL4695767 0.82 ADRA1D (0.71) SMN1; SMN2BLMADRA1DADRA1AADRA1B
SCHEMBL4696868 0.82 ADRA1D (0.71) SMN1; SMN2BLMADRA1DADRA1AADRA1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12605345-B2 Transdermal drug delivery system BioPhysics Pharma, Inc. (US) 2026-04-21 US claimed
US-20250268841-A1 Trans-Epithelial Membrane Drug Delivery System Masiz, John J. (US) 2025-08-28 US claimed
US-20250120907-A1 Transmucosal Drug Delivery System Masiz, John J. (US) 2025-04-17 US claimed
US-12246098-B2 Trans-epithelial membrane drug delivery system BioPhysics Pharma, Inc. (US) 2025-03-11 US claimed
US-20240216292-A1 Trans-Epithelial Membrane Drug Delivery System Masiz, John J. (US) 2024-07-04 US claimed
US-20240108588-A1 Transdermal Drug Delivery System Masiz, John J. (US) 2024-04-04 US claimed
US-11865217-B2 Transdermal drug delivery system BioPhysics Pharma, Inc. (US) 2024-01-09 US claimed
EP-4106816-A1 TRANSMUCOSAL DRUG DELIVERY SYSTEM North Atlantic Holdings LLC (US) 2022-12-28 EP claimed
US-20220387343-A1 Transdermal Drug Delivery System Masiz, John J. (US) 2022-12-08 US claimed
US-11446257-B2 Transdermal drug delivery system BioPhysics Pharma, Inc. (US) 2022-09-20 US claimed
WO-2008126088-A2 ANTI-PYRETIC VASODILATORS ZACHAR ORON (IL) 2008-10-23 WO claimed
EP-1641446-A1 PHARMACEUTICAL COMPOSITIONS INCLUDING AN ANTIHISTAMINE AND A STIMULANT AND USE THEREOF Pediamed Pharmaceuticals, Inc. (US) 2006-04-05 EP claimed
WO-2004112771-A1 PHARMACEUTICAL COMPOSITIONS INCLUDING AN ANTIHISTAMINE AND A STIMULANT AND USE THEREOF PEDIAMED PHARMACEUTICALS, INC. (US) 2004-12-29 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
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
US-5561154-A MUSCLE RELAXANTS INSTITUT DE RECHERCHES CHIMIQUES ET BIOLOQUES APPLIQUEES IRCEBA (FR) 1996-10-01 US claimed
EP-0728479-A1 Deacetyl moxisylyte in the treatment of acute urinary retention INSTITUT DE RECHERCHES CHIMIQUES ET BIOLOGIQUES APPLIQUEES (IRCEBA) (FR) 1996-08-28 EP claimed
US-5451609-A DEACETLY MOXISYLYTE INSTITUT DE RECHERCHES CHIMIQUES ET AL (FR) 1995-09-19 US claimed
US-5182270-A Inclusion compound with dimethyl-beta-cyclodextrin IOLAB CORPORATION (US) 1993-01-26 US claimed
EP-0031184-A1 Process for the preparation of 4-(2-(dimethylamino)-ethoxy)-2-methyl-5-(1-methylethyl)-phenol esters and their salts BLASCHIM S.p.A. (IT) 1981-07-01 EP claimed

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-12605345-B2 Transdermal drug delivery system FABP2, VEGFA, CUTA ADRA1D 94/4885ADRA1A 159/4885ADRA1B 296/4885

“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.