Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL108879

CCCC[N+](CCCC)(CCCC)CCCC.O=C(O)c1ccccc1

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1SDPP4HTR1BHTR1D

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
TSHR P16473 2/20 0.54
DAO P14920 1/20 0.54
NAPRT Q6XQN6 1/20 0.54
CES2 O00748 4/20 0.53
CES1 P23141 4/20 0.53
RARB P10826 6/20 0.50
NAAA Q02083 1/20 0.50
TP53 P04637 1/20 0.50
PLA2G4B P0C869 1/20 0.49
MEN1 O00255 1/20 0.49
ALDH1A1 P00352 1/20 0.49
RARA P10276 1/20 0.49
MAPT P10636 1/20 0.49
MTOR P42345 1/20 0.49
KMT2A Q03164 1/20 0.49

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 SCHEMBL23045181 1.00 TSHR (0.54) TSHRDAONAPRTCES2CES1
Tetrabuthylammonium SCHEMBL28983967 0.98 TSHR (0.52) TSHRDAONAPRTCES2CES1
Tetrabuthylammonium SCHEMBL28609595 0.98 TSHR (0.52) TSHRDAONAPRTCES2CES1
Benzoic Acid SCHEMBL10945586 0.96 CES2 (0.50) TSHRDAONAPRTCES2CES1
Tetrapentylammonium SCHEMBL10947994 0.96 TSHR (0.54) TSHRDAONAPRTCES2CES1
Tetrabuthylammonium SCHEMBL8579550 0.95 NAAA (0.50) TSHRDAONAPRTCES2CES1
Tetrahexylammonium SCHEMBL868317 0.94 CES2 (0.54) TSHRDAONAPRTCES2CES1
Benzoic Acid SCHEMBL9792086 0.94 CES2 (0.54) TSHRDAONAPRTCES2CES1
Tetrabuthylammonium SCHEMBL9513881 0.93 SRD5A2 (0.60) TSHRDAONAPRTCES2CES1
Tetrabuthylammonium SCHEMBL108444 0.92 RARB (0.58) TSHRRARBTP53PLA2G4BMEN1

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 1189 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3935114-B1 PROTECTIVE COATING COMPOSITION AND COATED METALLIC SUBSTRATE COMPRISING SAME MOMENTIVE PERFORMANCE MAT INC (US) 2025-07-16 EP claimed
US-12331214-B2 Resistant 2K-PUR coatings COVESTRO INTELLECTUAL PROPERTY GMBH & CO. KG (DE) 2025-06-17 US claimed
EP-4352449-B1 PROJECTILE PAYLOAD FOR TRAINING AMMUNITION WITH MULTI-SPECTRAL OUTPUT CYALUME TECH INC (US) 2025-05-07 EP claimed
EP-3994192-B1 RESISTANT 2K-PUR COATINGS COVESTRO DEUTSCHLAND AG (DE) 2025-04-30 EP claimed
CN-119823109-A An electrochromic material electrochromic composition and electrochromic device 吉林大学 2025-04-15 CN claimed
WO-2024081696-A2 COMPOSITIONS CONTAINING PHASE CHANGE MATERIALS, METHODS FOR FORMING OBJECTS USING THE SAME, AND METHOD FOR USING THE SAME PHASE CHANGE ENERGY SOLUTIONS, INC. (US) 2024-04-18 WO claimed
EP-4352449-A2 PROJECTILE PAYLOAD FOR TRAINING AMMUNITION WITH MULTI-SPECTRAL OUTPUT Cyalume Technologies, Inc (US) 2024-04-17 EP claimed
US-11939490-B2 Curable surface-protective coating composition, processes for its preparation and application to a metallic substrate and resulting coated metallic substrate MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2024-03-26 US claimed
US-11940253-B2 Projectile payload for training ammunition with multi-spectral output CYALUME TECHNOLOGIES, INC. (US) 2024-03-26 US claimed
CN-111117594-B Electrochromic material and electrochromic device based on dynamic metal-ligand complexation 吉林大学 2024-03-26 CN claimed
US-20050090627-A1 Low-temperature-curing epoxy-functional powder coating compositions DEGUSSA AG (DE) 2005-04-28 US claimed
US-6706908-B2 GROUP 8, 9, OR 10 METAL SOURCE (PALLADIUM ACETYLACETONATE); GROUP 2 METAL SOURCE (COPPER(II) 2,4-PENTANEDIONATE); AND GROUP 4 METAL SOURCE (TITANIUM(IV) OXIDE 2,4-PENTANEDIONATE); BENZOATE, ACETATE, SULFATE, OR NITRATE GENERAL ELECTRIC COMPANY 2004-03-16 US claimed
US-6700008-B2 USING CARBONYLATION CATALYST GENERAL ELECTRIC COMPANY 2004-03-02 US claimed
US-20030040428-A1 Method and catalyst composition for producing aromatic carbonates SHALYAEV KIRILL VLADIMIROVICH (US) 2003-02-27 US claimed
US-20020177521-A1 Method and catalyst composition for producing aromatic carbonates SHALYAEV KIRILL VLADIMIROVICH (US) 2002-11-28 US claimed
US-6440893-B1 GROUP 8, 9, OR 10 METAL SOURCE, INORGANIC COCATALYSTS OF GROUP 4 METAL SOURCE AND AT LEAST ONE GROUP 14 METAL SOURCE, AT LEAST ONE SALT COCATALYST ANION SELECTED FROM CARBOXYLATE, BENZOATE, ACETATE, SULFATE, NITRATE; FREE OF A HALIDE SOURCE GENERAL ELECTRIC COMPANY 2002-08-27 US claimed
US-6440892-B1 GROUP 8, 9, OR 10 METAL SOURCE, INORGANIC COCATALYSTS OF GROUP 4 METAL SOURCE AND AT LEAST ONE GROUP 11 METAL SOURCE, AT LEAST ONE SALT COCATALYST ANION SELECTED FROM CARBOXYLATE, BENZOATE, ACETATE, SULFATE, NITRATE; FREE OF A HALIDE SOURCE GENERAL ELECTRIC COMPANY 2002-08-27 US claimed
US-5705103-A Composition for producing chemiluminescent light of controllable duration JAME FINE CHEMICALS, INC. (US) 1998-01-06 US claimed
US-5597517-A OXALATE ESTER, SOLVENT, ACTIVATOR, FLUORESCER JAME FINE CHEMICALS, INC. (US) 1997-01-28 US claimed
US-4522729-A CXONTACTING IMPORITIES WITH TETRAALKYLAMMONIUM SALT PHILLIPS PETROLEUM COMPANY (US) 1985-06-11 US claimed