SCHEMBL6573413

SCHEMBL6573413

O=[N+]([O-])c1ccc(-c2ccccc2)cc1NS

nearest known ligand 0.50

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ABCB1 P08183 7/20 0.50
APP P05067 2/20 0.50
CRHBP P24387 1/20 0.49
CRHR2 Q13324 1/20 0.49
ABCC1 P33527 5/20 0.48
KCNMA1 Q12791 1/20 0.47
ALDH1A1 P00352 2/20 0.45
TDP1 Q9NUW8 2/20 0.45
L3MBTL1 Q9Y468 2/20 0.45
MAPK1 P28482 1/20 0.45
CASP7 P55210 1/20 0.45
ACLY P53396 1/20 0.44
CYP3A4 P08684 1/20 0.42
CYP2C9 P11712 1/20 0.42
CYP2C19 P33261 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
EPAS1 Q99814 1/20 0.41
MAOA P21397 1/20 0.41

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
SCHEMBL11576133 0.80 ABCB1 (0.48) ABCB1APPCRHBPCRHR2ABCC1
SCHEMBL1663325 0.78 CRHBP (0.63) ABCB1CRHBPCRHR2ABCC1KCNMA1
SCHEMBL28299547 0.76 MAPK1 (0.60) KCNMA1ALDH1A1TDP1L3MBTL1MAPK1
SCHEMBL17742439 0.75 TDP1 (0.66) ABCB1CRHBPCRHR2ABCC1KCNMA1
SCHEMBL14314156 0.75 ACLY (0.54) ABCB1APPCRHBPCRHR2ABCC1
SCHEMBL2332567 0.74 L3MBTL1 (0.65) APPCRHBPCRHR2ALDH1A1TDP1
SCHEMBL15940303 0.74 APP (0.48) ABCB1APPCRHBPCRHR2ABCC1
SCHEMBL17548845 0.74 CRHBP (0.53) ABCB1CRHBPCRHR2ABCC1KCNMA1
SCHEMBL12661135 0.74 CRHBP (0.53) ABCB1CRHBPCRHR2ABCC1KCNMA1
SCHEMBL5595131 0.74 CRHBP (0.68) ABCB1CRHBPCRHR2ABCC1KCNMA1

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
CN-117899873-A Transition metal catalyst and preparation method and application thereof 厦门大学 2024-04-19 CN disclosed
EP-1091935-B1 METHOD FOR PREPARING 2-NITRO-5-(PHENYLTHIO)-ANILINES BAYER CHEMICALS AG (DE) 2004-04-21 EP disclosed
US-6552230-B1 Amination of a 2,4-dichloronitrobenzene with ammonia forming 5-chloro-2-nitroaniline which is reacted with a thiophenol; one pot process BAYER AKTIENGESELLSCHAFT (DE) 2003-04-22 US disclosed
EP-1091935-A2 METHOD FOR PREPARING 2-NITRO-5-(PHENYLTHIO)-ANILINES Bayer Aktiengesellschaft (DE) 2001-04-18 EP disclosed
WO-2000001669-A2 METHOD FOR PREPARING 2-NITRO-5-(PHENYLTHIO)-ANILINES BAYER AKTIENGESELLSCHAFT (DE) 2000-01-13 WO disclosed