Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL3417348

CCCC[N+](CCCC)(CCCC)CCCC.O.O.[F-]

nearest known ligand 0.86

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Tetrabuthylammonium. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SLC22A1 O15245 4/20 0.86
SLC22A2 O15244 1/20 0.73
ALDH1A1 P00352 1/20 0.65
TP53 P04637 1/20 0.65
CYP3A4 P08684 1/20 0.65
ALOX15 P16050 1/20 0.65
TSHR P16473 1/20 0.65
ALOX12 P18054 1/20 0.65
SMN1; SMN2 Q16637 1/20 0.65
HIF1A Q16665 1/20 0.65
HSD17B10 Q99714 1/20 0.65
DNM1 Q05193 6/20 0.58
APAF1 O14727 1/20 0.48
HSP90AA1 P07900 1/20 0.48
RAD52 P43351 1/20 0.48

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
Tetrabuthylammonium SCHEMBL8818249 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL7713436 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL209886 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL10478288 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL2794537 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL2705733 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL136460 1.00 SLC22A1 (0.86) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL4494449 0.97 SLC22A1 (0.80) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL14720249 0.97 SLC22A1 (0.80) SLC22A1SLC22A2ALDH1A1TP53CYP3A4
Tetrabuthylammonium SCHEMBL2794532 0.97 SLC22A1 (0.80) SLC22A1SLC22A2ALDH1A1TP53CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230390281-A1 OPIOID FOR USE TO REDUCE AND/OR DRUG ADDICTION DMK PHARMACEUTICALS CORPORATION 2023-12-07 US disclosed
US-11779581-B2 Opioid for use to reduce and/or treat drug addiction DMK PHARMACEUTICALS CORPORATION (US) 2023-10-10 US disclosed
US-20220226312-A1 OPIOID FOR USE TO REDUCE AND/OR TREAT DRUG ADDICTION DMK PHARMACEUTICALS CORPORATION 2022-07-21 US disclosed
US-11246865-B2 Opioid for use to reduce and/or treat drug addiction VERSI GROUP, LLC (US) 2022-02-15 US disclosed
US-20200121674-A1 AN OPIOID FOR USE TO REDUCE AND/OR TREAT DRUG ADDICTION DMK PHARMACEUTICALS CORPORATION 2020-04-23 US disclosed
WO-2018204163-A1 AN OPIOID FOR USE TO REDUCE AND/OR TREAT DRUG ADDICTION VERSI GROUP, LLC (US) 2018-11-08 WO disclosed
US-7678800-B2 2-(1H-indolylsulfanyl)-aryl amine derivatives for use in the treatment of affective disorders, pain, ADHD and stress urinary incontinence H. LUNDBECK A/S (DK) 2010-03-16 US disclosed
EP-1771415-B1 2- (1H-INDOLYLSULFANYL) -ARYL AMINE DERIVATIVES FOR USE IN THE TREATMENT OF AFFECTIVE DISORDERS, PAIN, ADHD AND STRESS URINARY INCONTINENCE LUNDBECK & CO AS H (DK) 2009-01-07 EP disclosed
US-20080027074-A1 2-(1H-Indolysulfanyl)-Aryl Amine Derivatives for Use in the Treatment of Affective Disorders, Pain, Adhd and Stress Urinary Incontinence H. LUNDBECK A/S (DK) 2008-01-31 US disclosed
US-20070197786-A1 ENANTIOMERICALLY PURE OPIOID DIARYLMETHYLPIPERAZINE ENTA HOLDING LLC 2007-08-23 US disclosed
WO-2000056714-A1 NOVEL COMPOUNDS ASTRAZENECA AB (SE) 2000-09-28 WO disclosed
CN-1030604-C Heterocyclic compounds GLAXO SPA (IT) 1996-01-03 CN disclosed
EP-0399645-B1 Tetrahydropyranyl derivatives, process for their preparation and pharmaceutical or veterinary compositions containing them BEECHAM GROUP PLC (GB) 1994-11-09 EP disclosed
CN-1064682-A The preparation method of heterogeneous ring compound GLAXO SPA (IT) 1992-09-23 CN disclosed
EP-0123543-B1 LEUKOTRIENE ANTAGONISTS, THEIR PRODUCTION AND USE AND COMPOSITIONS CONTAINING THEM MERCK FROSST CANADA INC. (CA) 1988-02-03 EP disclosed
EP-0203621-A1 C-20-modified macrolide derivatives ELI LILLY AND COMPANY (US) 1986-12-03 EP disclosed
US-4609744-A 4-oxo-benzopyran carboxylic acids MERCK FROSST CANADA INC. (CA) 1986-09-02 US disclosed
EP-0123543-A1 Leukotriene antagonists, their production and use and compositions containing them MERCK FROSST CANADA INC. (CA) 1984-10-31 EP disclosed
US-4443436-A BACTERICIDES ELI LILLY AND COMPANY (US) 1984-04-17 US disclosed
EP-0104028-A1 C-20-modified macrolide derivatives ELI LILLY AND COMPANY (US) 1984-03-28 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 (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-20200121674-A1 AN OPIOID FOR USE TO REDUCE AND/OR TREAT DRUG ADDICTION OPRM1, OPRK1, OPRD1 SLC22A1 2054/4885SLC22A2 2357/4885ALDH1A1 56/4885
US-20080027074-A1 2-(1H-Indolysulfanyl)-Aryl Amine Derivatives for Use in the Treatment of Affective Disorders, Pain, Adhd and Stress Urinary Incontinence SLC6A2, HTR2C, SLC6A3 SLC22A1 371/4885SLC22A2 338/4885ALDH1A1 139/4885
US-20070197786-A1 ENANTIOMERICALLY PURE OPIOID DIARYLMETHYLPIPERAZINE OPRM1, OPRK1, OPRL1 SLC22A1 912/4885SLC22A2 752/4885ALDH1A1 730/4885
US-11779581-B2 Opioid for use to reduce and/or treat drug addiction OPRM1, OPRK1, OPRD1 SLC22A1 1781/4885SLC22A2 2045/4885ALDH1A1 59/4885
US-20230390281-A1 OPIOID FOR USE TO REDUCE AND/OR DRUG ADDICTION OPRM1, OPRK1, OPRD1 SLC22A1 1911/4885SLC22A2 2212/4885ALDH1A1 55/4885
US-20220226312-A1 OPIOID FOR USE TO REDUCE AND/OR TREAT DRUG ADDICTION OPRM1, OPRK1, OPRD1 SLC22A1 1781/4885SLC22A2 2045/4885ALDH1A1 59/4885
US-11246865-B2 Opioid for use to reduce and/or treat drug addiction OPRM1, OPRK1, OPRD1 SLC22A1 1781/4885SLC22A2 2045/4885ALDH1A1 59/4885

“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.