Tert-Butylamine

Tert-Butylamine

SCHEMBL7107931

CC(C)(C)N.O=C(O)c1cccc(C=CCOC(=O)N(c2ccccc2)c2ccccc2)c1

nearest known ligand 0.48

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
CACNA1B Q00975 8/20 0.48
TTR P02766 3/20 0.41
EPOR P19235 1/20 0.39
FBP1 P09467 1/20 0.39
UNG P13051 1/20 0.39
PPARG P37231 1/20 0.38
MAOB P27338 2/20 0.38
P4HB P07237 1/20 0.38
MMP1 P03956 1/20 0.37
MMP2 P08253 1/20 0.37
MMP9 P14780 1/20 0.37
MMP12 P39900 1/20 0.37

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 SCHEMBL7659363 1.00 CACNA1B (0.48) CACNA1BTTREPORFBP1UNG
Tert-Butylamine SCHEMBL7650662 0.89 CACNA1B (0.40) CACNA1BTTRFBP1UNGPPARG
Tert-Butylamine SCHEMBL7105104 0.89 CACNA1B (0.40) CACNA1BTTRFBP1UNGPPARG
Tert-Butylamine SCHEMBL7657269 0.83 CYP4F2 (0.39) CACNA1BEPORMAOB
Tert-Butylamine SCHEMBL7657274 0.83 CYP4F2 (0.39) CACNA1BEPORMAOB
Tert-Butylamine SCHEMBL7109741 0.83 EPOR (0.43) CACNA1BEPORMAOB
Tert-Butylamine SCHEMBL7657275 0.81 HDAC3 (0.39) CACNA1BEPORMAOB
SCHEMBL7107759 0.81 MMP1 (0.47) EPORMAOBMMP1MMP2MMP9
Tert-Butylamine SCHEMBL7653777 0.81 CYSLTR2 (0.47) EPORMAOB
Tert-Butylamine SCHEMBL7112471 0.81 EPOR (0.46) EPORPPARGMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1013639-B1 Aryl carboxylic acid and tetrazole derivatives comprising a carbamoyloxy unit HOFFMANN LA ROCHE (CH) 2003-10-01 EP disclosed
US-6335459-B1 PROSTAGLANDIN I2 RECEPTOR MODULATORS; TREATING TISSUE NECROSIS, PREMATURE UTERINE CONTRACTION, GASTRIC ULCERATION, SEXUAL DYSFUNCTION, MENSTRUAL PAIN AND IMPROPER WOUND HEALING, IMMUNOREGULATION, PLATELET AGGREGATION OR NEUTROPHIL FUNCTION SYNTEX (U.S.A.) LLC 2002-01-01 US disclosed
EP-1013639-A1 Aryl carboxylic acid and tetrazole derivatives comprising a carbamoyloxy unit F. HOFFMANN-LA ROCHE AG (CH) 2000-06-28 EP disclosed