Tetrabuthylammonium

Tetrabuthylammonium

SCHEMBL9655398

CCCC[N+](CCCC)(CCCC)CCCC.CC[N+](CC)(CC)Cc1ccccc1.F[B-](F)(F)F.[Cl-]

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.40
MEN1 O00255 2/20 0.53
KMT2A Q03164 2/20 0.53
TP53 P04637 1/20 0.53
MAPK1 P28482 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
HTT P42858 2/20 0.51
DNM1 Q05193 6/20 0.50
CYP1A2 P05177 1/20 0.47
BCHE P06276 1/20 0.40
KDM4E B2RXH2 1/20 0.40
ALDH1A1 P00352 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
CHRNA7 P36544 2/20 0.40
CHRNB4 P30926 1/20 0.40
CHRNA3 P32297 1/20 0.40
PSMD14 O00487 1/20 0.40
HSP90AA1 P07900 1/20 0.40
MMP2 P08253 1/20 0.40
MC4R P32245 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
Tetrabuthylammonium SCHEMBL3864476 0.93 MEN1 (0.59) MEN1KMT2ATP53MAPK1SMN1; SMN2
Tetrabuthylammonium SCHEMBL10876238 0.92 DNM1 (0.57) MEN1KMT2ATP53MAPK1SMN1; SMN2
Tetrabuthylammonium SCHEMBL9136922 0.92 MEN1 (0.57) MEN1KMT2ATP53MAPK1SMN1; SMN2
SCHEMBL383279 0.90 DNM1 (0.51) MEN1KMT2ATP53MAPK1SMN1; SMN2
Tetrabuthylammonium SCHEMBL7114513 0.90 DNM1 (0.59) MEN1KMT2ATP53MAPK1SMN1; SMN2
Hexane SCHEMBL9016836 0.90 DNM1 (0.59) MEN1KMT2ATP53MAPK1SMN1; SMN2
Hydrochloric Acid SCHEMBL8527490 0.90 MEN1 (0.58) MEN1KMT2ATP53MAPK1SMN1; SMN2
Hydrochloric Acid SCHEMBL11126527 0.88 MEN1 (0.66) MEN1KMT2ATP53MAPK1SMN1; SMN2
SCHEMBL12558342 0.88 DNM1 (0.56) MEN1KMT2ATP53MAPK1SMN1; SMN2
Hydrochloric Acid SCHEMBL11129711 0.86 MEN1 (0.69) MEN1KMT2ATP53MAPK1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0127216-B1 PROCESS FOR THE PREPARATION OF 21-HYDROXY-20-KETO-DELTA16-STEROIDS AND INTERMEDIATE COMPOUNDS FORMED IN THIS PROCESS ROUSSEL-UCLAF (FR) 1992-01-02 EP disclosed
EP-0127216-A1 Process for the preparation of 21-hydroxy-20-keto-delta16-steroids and intermediate compounds formed in this process ROUSSEL-UCLAF (FR) 1984-12-05 EP disclosed