Tromethamine

Tromethamine

SCHEMBL7036899

CC(=O)OCC(O)COCC(O)COC(C)=O.NC(CO)(CO)CO

nearest known ligand 0.38

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 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.38
LMNA P02545 6/20 0.36
MEN1 O00255 3/20 0.36
KMT2A Q03164 3/20 0.36
MAPT P10636 4/20 0.36
ALDH1A1 P00352 4/20 0.36
USP2 O75604 4/20 0.36
CYP3A4 P08684 3/20 0.36
SMN1; SMN2 Q16637 3/20 0.36
HPGD P15428 1/20 0.36
TP53 P04637 1/20 0.36
MAPK1 P28482 1/20 0.36
POLB P06746 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
HSD17B10 Q99714 1/20 0.31
ADRB2 P07550 1/20 0.31
ADRB1 P08588 1/20 0.31
ADRB3 P13945 1/20 0.31
TSHR P16473 1/20 0.31
KDM4E B2RXH2 2/20 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
SCHEMBL6131221 0.84 TDP1 (0.48) TDP1LMNAMEN1KMT2AMAPT
SCHEMBL304203 0.78 TDP1 (0.54) TDP1LMNAMEN1KMT2AMAPT
SCHEMBL15096923 0.75 ALDH1A1 (0.50) TDP1LMNAMEN1KMT2AMAPT
Tromethamine SCHEMBL6569887 0.74 LMNA (0.48) LMNAMEN1KMT2AALDH1A1USP2
SCHEMBL17480802 0.74 TDP1 (0.48) TDP1LMNAMEN1KMT2AMAPT
SCHEMBL17482276 0.74 PRKCA (0.49) TDP1LMNAMEN1KMT2AKDM4E
SCHEMBL14528315 0.73 HSD17B10 (0.50) TDP1LMNAMEN1KMT2AMAPT
Hydroquinone SCHEMBL6353777 0.73 ADRB2 (0.46) TDP1LMNAMEN1KMT2AMAPT
SCHEMBL22985141 0.72 LMNA (0.50) TDP1LMNAMEN1KMT2AMAPT
Tromethamine SCHEMBL4431533 0.72 LMNA (0.46) LMNAMEN1KMT2AALDH1A1SMN1; 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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1290058-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC. (US) 2003-03-12 EP claimed
WO-2001088013-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC (US) 2001-11-22 WO claimed
CN-113805435-B Photoresist and method 台湾积体电路制造股份有限公司 2024-05-28 CN disclosed
CN-116009357-A Methods and compositions for improving photoresist patterning 台湾积体电路制造股份有限公司 2023-04-25 CN disclosed
CN-115494698-A Method for manufacturing semiconductor device and photoresist 台湾积体电路制造股份有限公司 2022-12-20 CN disclosed
CN-110660650-B Semiconductor device and method for manufacturing the same 台湾积体电路制造股份有限公司 2022-09-13 CN disclosed
CN-113805435-A Photoresist and method 台湾积体电路制造股份有限公司 2021-12-17 CN disclosed
CN-112305861-A Method for manufacturing semiconductor device 台湾积体电路制造股份有限公司 2021-02-02 CN disclosed
CN-111863601-A Method for manufacturing semiconductor device and photoresist 台湾积体电路制造股份有限公司 2020-10-30 CN disclosed
CN-105093826-B Photoresist and method 台湾积体电路制造股份有限公司 2020-01-14 CN disclosed
CN-110660650-A Semiconductor device and method for manufacturing the same 台湾积体电路制造股份有限公司 2020-01-07 CN disclosed
EP-1290058-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC. (US) 2003-03-12 EP disclosed
WO-2001088013-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC (US) 2001-11-22 WO disclosed