SCHEMBL8979288

SCHEMBL8979288

O=C(c1ccccc1)N(Cl)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.52
RAB9A P51151 2/20 0.52
TDP1 Q9NUW8 2/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
LMNA P02545 1/20 0.47
ADRA2C P18825 1/20 0.47
NPSR1 Q6W5P4 2/20 0.46
ALDH1A1 P00352 4/20 0.46
CES2 O00748 2/20 0.46
CES1 P23141 2/20 0.46
TSHR P16473 2/20 0.46
DAO P14920 1/20 0.46
NAPRT Q6XQN6 1/20 0.46
KMT2A Q03164 3/20 0.46
KDM4E B2RXH2 2/20 0.46
DEPTOR Q8TB45 1/20 0.46
POLB P06746 2/20 0.43
NPC1 O15118 1/20 0.43
HTT P42858 1/20 0.43
HPGD P15428 2/20 0.43

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
SCHEMBL9833884 0.87 CES2 (0.52) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL27558517 0.86 RAB9A (0.41) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL11416543 0.86 RAB9A (0.41) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL3730131 0.80 NPSR1 (0.50) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL11115139 0.80 NPSR1 (0.56) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL783891 0.80 CES1 (0.50) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL9849003 0.80 CES1 (0.50) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL29876664 0.80 CES1 (0.50) L3MBTL1RAB9ATDP1SMN1; SMN2LMNA
SCHEMBL11168544 0.80 CES1 (0.63) CES1
SCHEMBL2700283 0.79 ALDH1A1 (0.56) SMN1; SMN2NPSR1ALDH1A1NAPRTKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2020029647-A1 METHOD FOR SYNTHESIZING NUCLEOSIDE COMPOUND AND INTERMEDIATE THEREOF 广州市锐博生物科技有限公司 2020-02-13 WO claimed
US-4264709-A ETHYLENICALLY UNSATURATED MONOMERS EASTMAN KODAK COMPANY (US) 1981-04-28 US claimed
WO-2020029647-A1 METHOD FOR SYNTHESIZING NUCLEOSIDE COMPOUND AND INTERMEDIATE THEREOF 广州市锐博生物科技有限公司 2020-02-13 WO disclosed
CN-101223208-B Nitrogenated aromatic compound, process for production of the same, polymer, and proton conductive membrane JSR CORP 2012-06-06 CN disclosed
US-5514740-A SHEET OR FILM HAVING CUPRIC SULFIDE DISPERSED THEREIN DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1996-05-07 US disclosed
US-5296601-A Reaction of aromatic chloride with carbon monoxide and alcohol NIHON NOHYAKU CO., LTD. (JP) 1994-03-22 US disclosed
EP-0282266-B1 PROCESS FOR PRODUCING CARBOXYLIC ACID AMIDES OR ESTERS NIHON NOHYAKU CO., LTD. (JP) 1992-09-09 EP disclosed
US-5142057-A Reacting an organic chloride with carbon monoxide and amine NIHON NOHYAKU CO., LTD. (JP) 1992-08-25 US disclosed
EP-0282266-A2 Process for producing carboxylic acid amides or esters NIHON NOHYAKU CO., LTD. (JP) 1988-09-14 EP disclosed
US-4264709-A ETHYLENICALLY UNSATURATED MONOMERS EASTMAN KODAK COMPANY (US) 1981-04-28 US disclosed
US-4202814-A AZO DYES GIVING FAST RED COLOR CIBA-GEIGY CORPORATION (US) 1980-05-13 US disclosed