Aniline

Aniline

SCHEMBL7517441

Nc1ccccc1.O=C(O)C(Cl)(Cl)Cl

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.55
ALDH1A1 P00352 4/20 0.50
CYP1A2 P05177 2/20 0.50
TP53 P04637 1/20 0.50
SMN1; SMN2 Q16637 2/20 0.45
HIF1A Q16665 1/20 0.45
PBRM1 Q86U86 1/20 0.43
TDP1 Q9NUW8 3/20 0.40
CYP3A4 P08684 2/20 0.40
HSD17B10 Q99714 2/20 0.40
TAAR1 Q96RJ0 1/20 0.40
MAPT P10636 3/20 0.39
KMT2A Q03164 3/20 0.39
MEN1 O00255 2/20 0.39
HPGD P15428 2/20 0.39
MAPK1 P28482 1/20 0.39
HTT P42858 1/20 0.39
L3MBTL1 Q9Y468 2/20 0.39
POLB P06746 1/20 0.39
PARP1 P09874 1/20 0.39

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
Diphenylamine SCHEMBL27959134 0.88 MAPT (0.58) TSHRALDH1A1CYP1A2SMN1; SMN2TDP1
Trichloroacetic Acid SCHEMBL6599928 0.85 TSHR (0.50) TSHRALDH1A1CYP1A2TP53SMN1; SMN2
Benzidine SCHEMBL11743215 0.83 ALDH1A1 (0.52) TSHRALDH1A1CYP1A2TP53SMN1; SMN2
Aniline SCHEMBL8413315 0.81 TSHR (0.73) TSHRALDH1A1CYP1A2PBRM1TDP1
Aniline SCHEMBL28088182 0.81 TSHR (0.73) TSHRALDH1A1CYP1A2SMN1; SMN2TDP1
Aniline SCHEMBL6049858 0.81 TSHR (0.73) TSHRALDH1A1CYP1A2PBRM1TDP1
Aniline SCHEMBL3769652 0.80 TSHR (0.55) TSHRCYP1A2SMN1; SMN2HIF1APBRM1
Dalfampridine SCHEMBL11585366 0.79 ALDH1A1 (0.56) TSHRALDH1A1CYP1A2TP53SMN1; SMN2
Trichloroacetic Acid SCHEMBL7743410 0.79 ACHE (0.56) TSHRALDH1A1CYP1A2TP53SMN1; SMN2
Aniline SCHEMBL4894770 0.78 TSHR (0.69) TSHRALDH1A1CYP1A2PBRM1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2002020544-A1 PROCESS FOR PREPARING PEPTIDE DERIVATIZED OLIGOMERIC COMPOUNDS ISIS PHARMACEUTICALS, INC. (US) 2002-03-14 WO disclosed
EP-1181301-A1 OLIGONUCLEOTIDE SYNTHESIS WITH LEWIS ACIDS AS ACTIVATORS ABBOTT LABORATORIES (US) 2002-02-27 EP disclosed
EP-1165575-A1 PHOSPHATE CONTAINING MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 2002-01-02 EP disclosed
WO-2000075157-A1 OLIGONUCLEOTIDE SYNTHESIS WITH LEWIS ACIDS AS ACTIVATORS ABBOTT LABORATORIES (US) 2000-12-14 WO disclosed
WO-2000058318-A1 PHOSPHATE CONTAINING MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 2000-10-05 WO disclosed
US-5574146-A Oligonucleotide synthesis with substituted aryl carboxylic acids as activators BECKMAN INSTRUMENTS, INC. (US) 1996-11-12 US disclosed
EP-0725787-A1 ACTIVATED NUCLEOSIDE PHOSPHORAMIDITES AND METHODS FOR THE PREPARATION AND USE THEREOF BECKMAN INSTRUMENTS, INC. (US) 1996-08-14 EP disclosed
WO-1996006853-A1 ACTIVATED NUCLEOSIDE PHOSPHORAMIDITES AND METHODS FOR THE PREPARATION AND USE THEREOF BECKMAN INSTRUMENTS, INC. (US) 1996-03-07 WO disclosed
EP-0003263-B1 A METHOD OF FORMING AN IMAGE, AND AN IMAGING ELEMENT FOR INHIBITING IMAGE FORMATION WITH COBALT (III) COMPLEXES EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1982-09-29 EP disclosed
US-4273860-A INCLUDING A PHOTOINHIBITOR TO SUPPRESS DECOMPOSITION OF THE COBALT COMPLEX USING RADIATION OF WAVELENGTHS LONGER THAN 300NM; NEGATIVES AND POSITIVES EASTMAN KODAK COMPANY (US) 1981-06-16 US disclosed
EP-0003263-A1 A method of forming an image, and an imaging element for inhibiting image formation with cobalt (III) complexes EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1979-08-08 EP disclosed
WO-1979000448-A1 INHIBITING IMAGE FORMATION WITH COBALT(III)COMPLEXES EASTMAN KODAK CO (US) 1979-07-26 WO disclosed