Tetrylammonium

Tetrylammonium

SCHEMBL1815477

CC[N+](CC)(CC)CC.O=S(=O)(O)c1ccccc1

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BTKCACNA1CCACNA1DCACNA1FCACNA1SCACNA2D1CACNA2D2DRD2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQHRH1HTR2AP2RY12

The experimentally established mechanism targets of Tetrylammonium. 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
TSHR P16473 3/20 0.67
SMN1; SMN2 Q16637 1/20 0.67
PSIP1 O75475 1/20 0.50
CYP2D6 P10635 2/20 0.47
POLB P06746 2/20 0.47
HSD11B1 P28845 2/20 0.44
ALDH1A1 P00352 4/20 0.41
CYP2C19 P33261 1/20 0.41
LMNA P02545 2/20 0.41
HTR6 P50406 1/20 0.41
MAPK1 P28482 1/20 0.41
KDM4E B2RXH2 2/20 0.40
MAPT P10636 1/20 0.40
NT5E P21589 1/20 0.40
TDP1 Q9NUW8 2/20 0.39
HSD17B10 Q99714 1/20 0.39
NAPRT Q6XQN6 1/20 0.39
CA1 P00915 1/20 0.39
CA2 P00918 1/20 0.39
MMP1 P03956 1/20 0.39

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
SCHEMBL330933 0.87 TSHR (0.55) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Propane SCHEMBL28882618 0.87 TSHR (0.80) TSHRSMN1; SMN2PSIP1CYP2D6POLB
SCHEMBL27464245 0.85 TSHR (0.76) TSHRSMN1; SMN2PSIP1CYP2D6POLB
SCHEMBL3719208 0.85 TSHR (0.76) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Alcohol SCHEMBL281881 0.85 TSHR (0.76) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Butane SCHEMBL2906063 0.85 TSHR (0.76) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Hydrogen Sulfide SCHEMBL7867594 0.84 TSHR (0.94) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Hydrogen Sulfide SCHEMBL10627246 0.84 TSHR (0.94) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Hydrogen Sulfide SCHEMBL28188397 0.84 TSHR (0.94) TSHRSMN1; SMN2PSIP1CYP2D6POLB
Benzene SCHEMBL28307046 0.84 TSHR (0.94) TSHRSMN1; SMN2PSIP1CYP2D6POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117822001-A Method for preparing benzyl alcohol and derivatives thereof through electrochemical catalysis 宁夏大学 2024-04-05 CN claimed
EP-4689232-A2 SUSTAINABLE PREPARATION OF HEXAMETHYLENE DIISOCYANATE FOR THE PRODUCTION OF POLYURETHANE Covestro Deutschland AG (DE) 2026-02-11 EP disclosed
CN-120060870-A Method for synthesizing dihydronaphthalene-1 (2H) -ketone by oxidizing styrene and derivatives thereof 宁夏大学 2025-05-30 CN disclosed
WO-2024208940-A2 SUSTAINABLE PREPARATION OF HEXAMETHYLENE DIISOCYANATE FOR THE PRODUCTION OF POLYURETHANE COVESTRO DEUTSCHLAND AG (DE) 2024-10-10 WO disclosed
EP-4442859-A1 SUSTAINABLE PRODUCTION OF HEXAMETHYLENE DIISOCYANATE FOR THE PRODUCTION OF POLYURETHANE Covestro Deutschland AG (DE) 2024-10-09 EP disclosed
CN-117822001-A Method for preparing benzyl alcohol and derivatives thereof through electrochemical catalysis 宁夏大学 2024-04-05 CN disclosed
WO-2019129783-A9 METHOD FOR PREPARING 2,7-OCTADIENE-1-OL TECHNOLOGIES MOLECULAIRES TECMO (FR) 2019-09-12 WO disclosed
CN-102977309-B Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSU CHEMICALS INC 2015-04-15 CN disclosed
US-8598257-B2 Polycarbonate resin composition CHEIL INDUSTRIES INC. (KR) 2013-12-03 US disclosed
CN-102066450-B Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSUI CHEMICALS INC 2013-11-06 CN disclosed
US-6423813-B1 FROM PHENOLIC COMPOUNDS TEIJIN LIMITED (JP) 2002-07-23 US disclosed
EP-1191049-A1 POLYCARBONATE, PROCESS FOR PRODUCING THE SAME, AND MOLDED ARTICLE THEREOF TEIJIN LIMITED (JP) 2002-03-27 EP disclosed
EP-1179556-A1 BRANCHED AROMATIC POLYCARBONATE, PROCESS FOR PRODUCING THE SAME, AND BLOW-MOLDED ARTICLE THEREOF TEIJIN LIMITED (JP) 2002-02-13 EP disclosed
US-6346569-B1 DISPERSING FEED POLYSUCCINIMIDE WITH DISPERSANT, REACTING DISPERSED POLYSUCCINIMIDE WITH CROSS-LINKING AGENT MITSUI CHEMICALS, INC. (JP) 2002-02-12 US disclosed
US-6103827-A A TRANSPARENT THERMOPLASTIC RESIN BLENDS GENERAL ELECTRIC COMPANY (US) 2000-08-15 US disclosed
US-6072024-A Production process of cross-linked polyaspartic acid resin MITSUI CHEMICALS, INC. (JP) 2000-06-06 US disclosed
US-5883194-A RADIATION TRANSPARENT THERMOPLASTIC RESINS OF CARBONATE AND ESTER BLENDS WITH ACRYLATE RESINS AND CATALYSTS GENERAL ELECTRIC COMPANY (US) 1999-03-16 US disclosed
EP-0866084-A2 Production process of cross-linked polyaspartic acid resin Mitsui Chemicals, Inc. (JP) 1998-09-23 EP disclosed
CN-1141935-A Thermoplastic resin composition GEN ELECTRICS CORP (US) 1997-02-05 CN disclosed
EP-0736574-A2 Thermoplastic resin composition comprising carbonate and acrylic resin GENERAL ELECTRIC COMPANY (US) 1996-10-09 EP disclosed