Tromethamine

Tromethamine

SCHEMBL8573552

CNCO.Cl.NC(CO)(CO)CO

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DHFRGARTPTGFRPTGIRPTGS1PTGS2TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8envmurAthyA

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.59
LMNA P02545 1/20 0.59
KMT2A Q03164 1/20 0.59
S1PR1 P21453 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
Tromethamine SCHEMBL8530527 1.00 MEN1 (0.59) MEN1LMNAKMT2AS1PR1
Tromethamine SCHEMBL466420 0.97 MEN1 (0.62) MEN1LMNAKMT2A
Tromethamine SCHEMBL2898170 0.85 MEN1 (0.48) MEN1LMNAKMT2A
Tromethamine SCHEMBL2862081 0.81 MEN1 (0.67) MEN1LMNAKMT2A
Tromethamine SCHEMBL9644059 0.81 MEN1 (0.77) MEN1LMNAKMT2AS1PR1
Tromethamine SCHEMBL445853 0.80 MEN1 (0.91) MEN1LMNAKMT2AS1PR1
Tromethamine SCHEMBL1270294 0.80 MEN1 (0.91) MEN1LMNAKMT2AS1PR1
Tromethamine SCHEMBL2188 0.80
Tromethamine SCHEMBL2313359 0.80 MEN1 (0.91) MEN1LMNAKMT2AS1PR1
Tromethamine SCHEMBL1524832 0.80 MEN1 (0.91) MEN1LMNAKMT2AS1PR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-100357267-C Use of 2, 4-diamino-3-hydroxycarboxylic acid derivatives as proteasome inhibitors NOVARTIS AG (CH) 2007-12-26 CN disclosed
CN-1351587-A Use of 2,4-diamino-3-hydroxycarboxylic acid derivatives as proteasome inhibitors NOVARTIS AG (CH) 2002-05-29 CN disclosed
WO-1998015541-A1 NOVEL ISOXAZOL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME, AND A PROCESS FOR THE PREPARATION OF THE NOVEL COMPOUNDS EGIS Gyógyszergyár Rt. (HU) 1998-04-16 WO disclosed
EP-0449812-B1 METHOD OF PRE-TREATING SAMPLES IN PEROXIDASE-CATALYZED ENZYME ASSAYS SANOFI DIAGNOSTICS PASTEUR INC (US) 1995-09-13 EP disclosed
WO-1995005376-A1 SUBSTITUTED 2(5H)FURANONE, 2(5H)THIOPHENONE AND 2(5H)PYRROLONE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS ENDOTHELIN ANTAGONISTS WARNER-LAMBERT COMPANY (US) 1995-02-23 WO disclosed
WO-1993021219-A1 ENDOTHELIN ANTAGONISTS II WARNER-LAMBERT COMPANY (US) 1993-10-28 WO disclosed
WO-1993008122-A1 CONTRAST AGENTS AND COMPOSITIONS FOR RADIOLOGICAL IMAGING, AND RADIOLOGICAL IMAGING METHOD UTILIZING SAME GUERBET S.A. (FR) 1993-04-29 WO disclosed
EP-0449812-A4 METHOD OF PRE-TREATING SAMPLES IN PEROXIDASE-CATALYZED ENZYME ASSAYS 1991-10-30 EP disclosed
EP-0449812-A1 METHOD OF PRE-TREATING SAMPLES IN PEROXIDASE-CATALYZED ENZYME ASSAYS. KALLESTAD DIAGNOSTICS INC (US) 1991-10-09 EP disclosed
WO-1990007115-A1 METHOD OF PRE-TREATING SAMPLES IN PEROXIDASE-CATALYZED ENZYME ASSAYS KALLESTAD DIAGNOSTICS, INC. (US) 1990-06-28 WO disclosed