Gallamine

Gallamine

SCHEMBL12638600

CC[N+](CC)(CC)CCOc1cccc(OCC[N+](CC)(CC)CC)c1OCC[N+](CC)(CC)CC

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRNA1CHRNB1CHRNDCHRNECHRNG

The experimentally established mechanism targets of Gallamine. 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
CHRM2 P08172 2/20 1.00
ALOX15 P16050 2/20 1.00
LMNA P02545 1/20 1.00
CHRM1 P11229 1/20 1.00
TSHR P16473 1/20 1.00
ACHE P22303 1/20 1.00
KCNH2 Q12809 1/20 1.00
HIF1A Q16665 1/20 1.00
CHRNA7 P36544 16/20 0.56
CHRNB4 P30926 12/20 0.56
CHRNA3 P32297 12/20 0.56
CHRNB2 P17787 9/20 0.56
CHRNA4 P43681 9/20 0.56
SMN1; SMN2 Q16637 1/20 0.47
MAPT P10636 1/20 0.46
KDM4E B2RXH2 1/20 0.46
MEN1 O00255 1/20 0.46
ALDH1A1 P00352 1/20 0.46
TP53 P04637 1/20 0.46
CYP1A2 P05177 1/20 0.46

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
Gallamine SCHEMBL249090 0.98 CHRM2 (1.00) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL19300483 0.95 CHRM2 (0.90) CHRM2ALOX15LMNACHRM1TSHR
Gallamine SCHEMBL1736255 0.93 CHRM2 (0.87) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL16884476 0.87 CHRM2 (0.77) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL8557526 0.77 LMNA (0.62) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL3265285 0.77 CHRM2 (0.59) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL1238407 0.75 LMNA (0.60) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL13658189 0.73 LMNA (0.58) CHRM2ALOX15LMNACHRM1TSHR
SCHEMBL13385235 0.72 CHRNA7 (1.00) ALOX15CHRNA7CHRNB4CHRNA3CHRNB2
SCHEMBL456438 0.72 CHRM2 (0.56) CHRM2ALOX15LMNACHRM1TSHR

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250179130-A1 METHODS AND SYSTEMS FOR DESIGNING AND/OR CHARACTERIZING SOLUBLE LIPIDATED LIGAND AGENTS ON TARGET THERAPEUTICS LLC 2025-06-05 US disclosed
CN-118613258-A Esters of 8-methyl-8-azabicyclo [3.2.1] oct-3-yl 3-hydroxy-2-phenylpropionate ADS医疗有限责任公司 2024-09-06 CN disclosed
US-12060397-B2 Soluble lipidated ligand agents for treating eye inflammation TUFTS MEDICAL CENTER (US) 2024-08-13 US disclosed
CN-108699013-B Spiroquinone derivative, method for preparing the same, and pharmaceutical composition for preventing or treating neurological disorders containing the same as an active ingredient 嘉泉大学校校产学协力团 2022-05-06 CN disclosed
US-20220135633-A1 METHODS AND SYSTEMS FOR DESIGNING AND/OR CHARACTERIZING SOLUBLE LIPIDATED LIGAND AGENTS ON TARGET THERAPEUTICS LLC 2022-05-05 US disclosed
CN-114341343-A Alpha-synuclein assay 才思治疗公司 2022-04-12 CN disclosed
US-10233219-B2 Methods and systems for designing and/or characterizing soluble lipidated ligand agents TUFTS MEDICAL CENTER (US) 2019-03-19 US disclosed
US-9956229-B2 Acyclic cucurbit[n]uril type molecular containers to treat intoxication and decrease relapse rate in substance abuse disorders UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2018-05-01 US disclosed
US-20170246180-A1 ACYCLIC CUCURBIT[N]URIL TYPE MOLECULAR CONTAINERS TO TREAT INTOXICATION AND DECREASE RELAPSE RATE IN SUBSTANCE ABUSE DISORDERS GENERAL HOSPITAL CORPORATION 2017-08-31 US disclosed
US-9469648-B2 Reversal of drug-induced neuromuscular block using novel molecular containers UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2016-10-18 US disclosed
WO-2016061571-A1 ACYCLIC CUCURBIT(N)URIL TYPE MOLECULAR CONTAINERS TO TREAT INTOXICATION AND DECREASE RELAPSE RATE IN SUBSTANCE ABUSE DISORDERS UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2016-04-21 WO disclosed
US-20160052982-A1 METHODS AND SYSTEMS FOR DESIGNING AND/OR CHARACTERIZING SOLUBLE LIPIDATED LIGAND AGENTS ON TARGET THERAPEUTICS LLC 2016-02-25 US disclosed
WO-2013074059-A2 CYTOSINE DEAMINASE MODULATORS FOR ENHANCEMENT OF DNA TRANSFECTION REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2013-05-23 WO disclosed
US-20130071786-A1 COATING COMPOSITION AND IMAGE-FORMING MATERIAL, LITHOGRAPHIC PRINTING PLATE PRECURSOR AND OXYGEN-BLOCKING FILM INCLUDING THE COATING COMPOSITION FUJIFILM CORPORATION (JP) 2013-03-21 US disclosed
US-20130071786-A1 COATING COMPOSITION AND IMAGE-FORMING MATERIAL, LITHOGRAPHIC PRINTING PLATE PRECURSOR AND OXYGEN-BLOCKING FILM INCLUDING THE COATING COMPOSITION FUJIFILM CORPORATION (JP) 2013-03-21 US disclosed
US-7947854-B2 Phospholipase inhibitor; prevention or therapy of microbial infection; bactericides; fungicides; viricides; parasiticides; using quaternary or phosphonium group containing compounds THE UNIVERSITY OF SYDNEY (AU) 2011-05-24 US disclosed
EP-2045662-A2 Lithographic printing plate precursor and method of preparing lithographic printing plate FUJIFILM Corporation (JP) 2009-04-08 EP disclosed
US-20080275003-A1 Bis-Cationic Compounds and Use Thereof THE UNIVERSITY OF SYDNEY (AU) 2008-11-06 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 (7 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-20220135633-A1 METHODS AND SYSTEMS FOR DESIGNING AND/OR CHARACTERIZING SOLUBLE LIPIDATED LIGAND AGENTS LDLR, HDLBP, LIPG CHRM2 2169/4885ALOX15 743/4885LMNA 2571/4885
US-20080275003-A1 Bis-Cationic Compounds and Use Thereof PLCB1, PLCB3, PLA2G4B CHRM2 3986/4885ALOX15 656/4885LMNA 841/4885
US-20170246180-A1 ACYCLIC CUCURBIT[N]URIL TYPE MOLECULAR CONTAINERS TO TREAT INTOXICATION AND DECREASE RELAPSE RATE IN SUBSTANCE ABUSE DISORDERS CNR1, CNR2, OPRM1 CHRM2 1069/4885ALOX15 3066/4885LMNA 3286/4885
US-20160052982-A1 METHODS AND SYSTEMS FOR DESIGNING AND/OR CHARACTERIZING SOLUBLE LIPIDATED LIGAND AGENTS LDLR, HDLBP, LIPG CHRM2 2169/4885ALOX15 743/4885LMNA 2571/4885
US-10233219-B2 Methods and systems for designing and/or characterizing soluble lipidated ligand agents LDLR, HDLBP, LIPG CHRM2 2169/4885ALOX15 743/4885LMNA 2571/4885
US-20250179130-A1 METHODS AND SYSTEMS FOR DESIGNING AND/OR CHARACTERIZING SOLUBLE LIPIDATED LIGAND AGENTS LDLR, HDLBP, LIPG CHRM2 2169/4885ALOX15 743/4885LMNA 2571/4885
US-12060397-B2 Soluble lipidated ligand agents for treating eye inflammation LIPG, CD40, LDLR CHRM2 1928/4885ALOX15 223/4885LMNA 3786/4885

“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.