Tromethamine

Tromethamine

SCHEMBL12466254

CC(O)N(C(C)O)C(C)O.NC(CO)(CO)CO

nearest known ligand 0.53

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 5)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.53
LMNA P02545 1/20 0.53
KMT2A Q03164 1/20 0.53
TDP1 Q9NUW8 1/20 0.32
ALDH1A1 P00352 1/20 0.30

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 SCHEMBL6210360 0.84 MEN1 (0.53) MEN1LMNAKMT2ATDP1ALDH1A1
Tromethamine SCHEMBL7567125 0.83 LMNA (0.67) MEN1LMNAKMT2ATDP1ALDH1A1
Tromethamine SCHEMBL8530728 0.82 MEN1 (0.36) MEN1LMNAKMT2A
Tromethamine SCHEMBL1155666 0.79 MEN1 (0.53) MEN1LMNAKMT2ATDP1
Tromethamine SCHEMBL9363390 0.78 MEN1 (0.59) MEN1LMNAKMT2ATDP1
Tromethamine SCHEMBL8334055 0.78 LMNA (0.59) MEN1LMNAKMT2ATDP1ALDH1A1
Tromethamine SCHEMBL4737664 0.76 MEN1 (0.56) MEN1LMNAKMT2ATDP1
Tromethamine SCHEMBL9547767 0.76 MEN1 (0.56) MEN1LMNAKMT2ATDP1ALDH1A1
Tromethamine SCHEMBL4735605 0.76 MEN1 (0.56) MEN1LMNAKMT2ATDP1
Tromethamine SCHEMBL9443897 0.75 MEN1 (0.62) MEN1LMNAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2668161-B1 METHOD AND SUBSTANCES FOR PREPARATION OF N-SUBSTITUTED PYRIDINIUM COMPOUNDS ROCHE DIAGNOSTICS GMBH (DE) 2014-11-26 EP disclosed
US-8754111-B2 Method and substances for preparation of N-substituted pyridinium compounds ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2014-06-17 US disclosed
EP-2668161-A1 METHOD AND SUBSTANCES FOR PREPARATION OF N-SUBSTITUTED PYRIDINIUM COMPOUNDS Roche Diagniostics GmbH (DE) 2013-12-04 EP disclosed
US-20130303768-A1 METHOD AND SUBSTANCES FOR PREPARATION OF N-SUBSTITUTED PYRIDINIUM COMPOUNDS ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2013-11-14 US disclosed
WO-2012101095-A1 METHOD AND SUBSTANCES FOR PREPARATION OF N-SUBSTITUTED PYRIDINIUM COMPOUNDS ROCHE DIAGNOSTICS GMBH (DE) 2012-08-02 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20130303768-A1 METHOD AND SUBSTANCES FOR PREPARATION OF N-SUBSTITUTED PYRIDINIUM COMPOUNDS PNMT, HNMT, CHRM5 MEN1 661/4885LMNA 829/4885KMT2A 756/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.