Tert-Butylamine

Tert-Butylamine

SCHEMBL10375334

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nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACEIDH1

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
FNTA P49354 1/20 0.41
FNTB P49356 1/20 0.41
CA1 P00915 1/20 0.37
CA2 P00918 1/20 0.37
CA4 P22748 1/20 0.37
CA7 P43166 1/20 0.37
MGAM O43451 1/20 0.31
GAA P10253 1/20 0.31
SI P14410 1/20 0.31
MGAM2 Q2M2H8 1/20 0.31
LMNA P02545 1/20 0.31
HTT P42858 1/20 0.31

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
Tert-Butylamine SCHEMBL10837638 1.00 FNTA (0.41) FNTAFNTBCA1CA2CA4
SCHEMBL3182370 0.89 FNTA (0.47) FNTAFNTBCA1CA2CA4
SCHEMBL28205206 0.89 FNTA (0.47) FNTAFNTBCA1CA2CA4
Ammonia Solution, Strong SCHEMBL9638545 0.86 FNTA (0.46) FNTAFNTBCA1CA2CA4
SCHEMBL27257292 0.86 FNTA (0.46) FNTAFNTBCA1CA2CA4
Fluoride SCHEMBL10492292 0.86 FNTA (0.46) FNTAFNTBCA1CA2CA4
Trimethylammonium SCHEMBL10838652 0.82 FNTA (0.43) FNTAFNTBCA1CA2CA4
SCHEMBL28257083 0.80 FNTA (0.42) FNTAFNTBCA1CA2CA4
SCHEMBL10969272 0.77 FNTA (0.40) FNTAFNTBCA1CA2CA4
N,N-Dimethylethanaminium SCHEMBL9638521 0.77 FNTA (0.40) FNTAFNTBCA1CA2CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0155634-B1 PROCESS FOR THE PREPARATION OF 6-METHYL-3,4-DIHYDRO-1,2,3-OXATHIAZIN-4-ONE 2,2-DIOXIDE AND OF ITS NON-TOXIC SALTS, AS WELL AS OF ACETOACETAMIDE-N-SULFONIC ACID OCCURRING AS AN INTERMEDIARY IN THIS PROCESS, AND ITS SALTS HOECHST AKTIENGESELLSCHAFT (DE) 1990-06-13 EP disclosed