SCHEMBL6563719

SCHEMBL6563719

O=S(=O)(O)c1ccc(N=Nc2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ POLB P06746 1/20 1.00
▸ CYP2D6 P10635 1/20 1.00
▸ TSHR P16473 2/20 0.62
▸ SMN1; SMN2 Q16637 1/20 0.62
▸ RPS6KA3 P51812 1/20 0.53
▸ PHLPP2 Q6ZVD8 1/20 0.53
▸ CYP2C19 P33261 1/20 0.52
▸ ALDH1A1 P00352 2/20 0.52
▸ MEN1 O00255 5/20 0.52
▸ KMT2A Q03164 5/20 0.52
▸ NPC1 O15118 2/20 0.52
▸ TRPA1 O75762 1/20 0.52
▸ MAPT P10636 3/20 0.52
▸ HPGD P15428 1/20 0.52
▸ ATIC P31939 1/20 0.49
▸ KDM4E B2RXH2 1/20 0.48
▸ HSP90AA1 P07900 1/20 0.48
▸ MAPK1 P28482 1/20 0.48
▸ TDP1 Q9NUW8 1/20 0.48
▸ LMNA P02545 1/20 0.48

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
SCHEMBL408153 1.00 POLB (1.00) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL28788411 0.98 POLB (0.96) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
Water SCHEMBL29032744 0.96 POLB (0.92) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL28560987 0.91 POLB (0.83) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL18624977 0.91 POLB (0.83) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL460752 0.85 POLB (0.73) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL460751 0.85 POLB (0.73) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL28560984 0.85 POLB (0.72) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL11291804 0.85 POLB (0.72) POLBCYP2D6TSHRSMN1; SMN2RPS6KA3
SCHEMBL27918619 0.85 MEN1 (0.73) POLBCYP2D6TSHRSMN1; SMN2PHLPP2

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 146 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119343022-A P-i-n perovskite solar cell based on light-dark reversible heterogeneous molecular stress release light circulation stability and preparation method thereof 河南大学 2025-01-21 — — CN claimed
CN-114351194-A Plating solution and process for electroplating copper on through hole of printed circuit 电子科技大学 2022-04-15 — — CN claimed
CN-1046701-C Process for preparing substituted aromatic amines MONSANTO CO (US) 1999-11-24 — — CN claimed
EP-0696269-B1 PROCESS FOR PREPARING SUBSTITUTED AROMATIC AMINES MONSANTO CO (US) 1999-06-30 — — EP claimed
CN-1216110-A Device for preserving and delivering gas-containing solutions BAXTER INT (US) 1999-05-05 — — CN claimed
US-5633407-A Process for preparing substituted aromatic amines FLEXSYS AMERICA L. P. (US) 1997-05-27 — — US claimed
EP-0641313-B1 PROCESS FOR PREPARING SUBSTITUTED AROMATIC AMINES MONSANTO CO (US) 1997-01-22 — — EP claimed
US-5552531-A USED IN THE PRODUCTION OF AROMATIC AMINES, REACTING A NUCLEOPHILIC ANILINE, OR AMIDE OR AMINE WITH AN AZO COMPOUND MONSANTO COMPANY (US) 1996-09-03 — — US claimed
CN-1121706-A Process for preparing substituted aromatic amines MONSANTO CO (US) 1996-05-01 — — CN claimed
EP-0696269-A1 PROCESS FOR PREPARING SUBSTITUTED AROMATIC AMINES MONSANTO COMPANY (US) 1996-02-14 — — EP claimed
US-5451702-A Process for preparing substituted aromatic amines MONSANTO COMPANY (US) 1995-09-19 — — US claimed
EP-0641313-A1 PROCESS FOR PREPARING SUBSTITUTED AROMATIC AMINES. MONSANTO CO (US) 1995-03-08 — — EP claimed
WO-1994025425-A1 PROCESS FOR PREPARING SUBSTITUTED AROMATIC AMINES MONSANTO COMPANY (US) 1994-11-10 — — WO claimed
WO-1993024450-A1 PROCESS FOR PREPARING SUBSTITUTED AROMATIC AMINES MONSANTO COMPANY (US) 1993-12-09 — — WO claimed
JP-11071223-A — — None — — JP disclosed
JP-11071232-A — — None — — JP disclosed
CN-119343022-A P-i-n perovskite solar cell based on light-dark reversible heterogeneous molecular stress release light circulation stability and preparation method thereof 河南大学 2025-01-21 — — CN disclosed
WO-1989009627-A1 NON-THROMBOGENIC INTRAVASCULAR CATHETER COATED WITH POLYMYXIN SHANBROM EDWARD (US) 1989-10-19 — — WO disclosed
WO-1989009626-A1 NON-THROMBOGENIC INTRAVASCULAR TIME RELEASE CATHETER LUTHER RONALD B (US) 1989-10-19 — — WO disclosed
EP-0326100-A2 Ion-capture assays and devices ABBOTT LABORATORIES (US) 1989-08-02 — — EP disclosed
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