Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL331004

CCCC[N+](CCCC)(CCCC)CCCC.CCS(=O)(=O)O

nearest known ligand 0.63

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FGFR1FGFR2FGFR3FGFR4FLT1FLT4KDRPDGFRAPDGFRB

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 14)

geneUniProtsupporting neighboursconfidence
SLC22A1 O15245 3/20 0.63
SLC22A2 O15244 1/20 0.55
TP53 P04637 2/20 0.50
ALDH1A1 P00352 1/20 0.50
CYP3A4 P08684 1/20 0.50
ALOX15 P16050 1/20 0.50
TSHR P16473 1/20 0.50
ALOX12 P18054 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
HIF1A Q16665 1/20 0.50
HSD17B10 Q99714 1/20 0.50
DNM1 Q05193 5/20 0.46
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40

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
SCHEMBL330865 0.95 SLC22A1 (0.62) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrahexylammonium SCHEMBL330970 0.92 SLC22A1 (0.65) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
SCHEMBL331696 0.92 SLC22A1 (0.65) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
SCHEMBL330482 0.92 SLC22A1 (0.65) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrabuthylammonium SCHEMBL27990806 0.92 SLC22A1 (0.67) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrabuthylammonium SCHEMBL243899 0.92 SLC22A1 (0.67) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrabuthylammonium SCHEMBL331036 0.90 SLC22A1 (0.63) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrabuthylammonium SCHEMBL9998667 0.90 SLC22A1 (0.63) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrabuthylammonium SCHEMBL28650063 0.90 SLC22A1 (0.63) SLC22A1SLC22A2TP53ALDH1A1CYP3A4
Tetrabuthylammonium SCHEMBL28652896 0.90 SLC22A1 (0.63) SLC22A1SLC22A2TP53ALDH1A1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2295484-B1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2018-01-17 EP disclosed
EP-2407498-B1 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSUI CHEMICALS INC (JP) 2017-11-15 EP disclosed
US-8304507-B2 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material MITSUI CHEMICALS, INC. (JP) 2012-11-06 US disclosed
EP-2407498-A2 Polymerizable composition for polythiourethane optical material, polythiourethane optical material obtained from the polymerizable composition, and polymerization catalyst for polythiourethane optical material Mitsui Chemicals, Inc. (JP) 2012-01-18 EP disclosed
US-20110112269-A1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM THE POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL MITSUI CHEMICALS, INC. (JP) 2011-05-12 US disclosed
EP-2295484-A1 POLYMERIZABLE COMPOSITION FOR POLYTHIOURETHANE OPTICAL MATERIAL, POLYTHIOURETHANE OPTICAL MATERIAL OBTAINED FROM SAME POLYMERIZABLE COMPOSITION, AND POLYMERIZATION CATALYST FOR POLYTHIOURETHANE OPTICAL MATERIAL Mitsui Chemicals, Inc. (JP) 2011-03-16 EP disclosed