Dimethylphenylpiperazinium

Dimethylphenylpiperazinium

SCHEMBL305083

C[N+]1(C)CCN(c2ccccc2)CC1.[I-]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNG

The experimentally established mechanism targets of Dimethylphenylpiperazinium. 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
MEN1 O00255 1/20 1.00
POLB P06746 1/20 1.00
APOBEC3A P31941 1/20 1.00
PMP22 Q01453 1/20 1.00
KMT2A Q03164 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
HIF1A Q16665 1/20 1.00
APOBEC3G Q9HC16 1/20 1.00
CHRNA7 P36544 2/20 0.96
CYP3A4 P08684 1/20 0.96
ALOX15 P16050 1/20 0.96
CHRNB2 P17787 1/20 0.96
NFKB1 P19838 1/20 0.96
MAPK1 P28482 1/20 0.96
CHRNA3 P32297 1/20 0.96
CHRNA4 P43681 1/20 0.96
HSD17B10 Q99714 1/20 0.96
HTR3E A5X5Y0 1/20 0.59
HTR3B O95264 1/20 0.59
HTR3A P46098 1/20 0.59

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
Dimethylphenylpiperazinium SCHEMBL3453554 0.98 CHRNA7 (1.00) MEN1POLBAPOBEC3APMP22KMT2A
Dimethylphenylpiperazinium SCHEMBL1427906 0.96 CHRNA7 (0.96) MEN1POLBAPOBEC3APMP22KMT2A
Dimethylphenylpiperazinium SCHEMBL6829257 0.96 CHRNA7 (0.96) MEN1POLBAPOBEC3APMP22KMT2A
Iodide SCHEMBL404487 0.92 MEN1 (0.85) MEN1POLBAPOBEC3APMP22KMT2A
SCHEMBL10114942 0.90 CHRNA7 (0.85) MEN1POLBAPOBEC3APMP22KMT2A
SCHEMBL10105152 0.79 CHRNA7 (0.72) MEN1POLBAPOBEC3APMP22KMT2A
SCHEMBL6743986 0.77 ALOX15 (0.64) MEN1POLBAPOBEC3APMP22KMT2A
SCHEMBL10105155 0.76 CHRNA7 (0.63) MEN1POLBAPOBEC3APMP22KMT2A
SCHEMBL164538 0.75 LMNA (0.67) MEN1POLBAPOBEC3APMP22KMT2A
SCHEMBL576454 0.75 LMNA (0.67) MEN1POLBAPOBEC3APMP22KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12331159-B2 Polyesters and polyketoesters from carbonylative terpolymerization of enols, methods to produce, blends, and articles therefrom EXXON MOBIL CHEMICAL PATENTS INC. (US) 2025-06-17 US claimed
CN-119356472-A Photovoltaic maximum power control method combining cubic spline interpolation and P & O improvement 西南石油大学 2025-01-24 CN claimed
US-20240373736-A1 Materials and Methods to Improve the Stability of Metal Halide Perovskites THE UNIVERSITY OF TOLEDO (US) 2024-11-07 US claimed
CN-115078490-B Be used for detecting CN–Preparation method of iridium (III) complex sensitized NiO photocathode 青岛科技大学 2024-04-30 CN claimed
US-11685755-B2 Dicarbonyl ruthenium and osmium catalysts Universita′ degli Studi di Udine (IT) 2023-06-27 US claimed
CN-115078490-A For detecting CN – Preparation method of iridium (III) complex sensitized NiO photocathode 青岛科技大学 2022-09-20 CN claimed
US-20220064375-A1 Polyesters and Polyketoesters from Carbonylative Terpolymerization of enols, Methods to Produce, Blends, and Articles Therefrom REGENTS OF THE UNIVERSITY OF MINNESOTA 2022-03-03 US claimed
US-7914960-B2 Additive containing charge transport layer photoconductors XEROX CORPORATION (US) 2011-03-29 US claimed
US-20090092913-A1 ADDITIVE CONTAINING PHOTOGENERATING LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 US claimed
US-20090092911-A1 ADDITIVE CONTAINING CHARGE TRANSPORT LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 US claimed
US-5861431-A Incontinence treatment IOTEK, INC. (US) 1999-01-19 US claimed
EP-0831772-A2 INTRAURETHRAL PHARMACOTHERAPY OF INCONTINENCE IOTEK, INC. (US) 1998-04-01 EP claimed
EP-0615855-B1 Recording sheets containing pyridinium and/or piperazinum compounds XEROX CORP (US) 1997-05-14 EP claimed
WO-1996040054-A2 INTRAURETHRAL PHARMACOTHERAPY OF INCONTINENCE IOTEK, INC. (US) 1996-12-19 WO claimed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 US claimed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 US claimed
US-5441795-A Piperazinium compounds XEROX CORPORATION (US) 1995-08-15 US claimed
EP-0615855-A1 Recording sheets containing pyridinium and/or piperazinum compounds XEROX CORPORATION (US) 1994-09-21 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 (2 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-11685755-B2 Dicarbonyl ruthenium and osmium catalysts OTC, ODC1, CBR3 MEN1 3163/4885POLB 518/4885APOBEC3A 2584/4885
US-20240373736-A1 Materials and Methods to Improve the Stability of Metal Halide Perovskites SOD1, BMI1, VCL MEN1 250/4885POLB 2214/4885APOBEC3A 494/4885

“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.