SCHEMBL6807684

SCHEMBL6807684

N#Cc1ccc(-c2nc3ccccc3s2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ APP P05067 8/20 0.63
▸ RAB9A P51151 6/20 0.63
▸ NPC1 O15118 5/20 0.63
▸ KDM4E B2RXH2 3/20 0.63
▸ GLA P06280 2/20 0.63
▸ GAA P10253 2/20 0.63
▸ MAPT P10636 2/20 0.63
▸ MMP9 P14780 2/20 0.63
▸ MMP8 P22894 2/20 0.63
▸ ALDH1A1 P00352 2/20 0.63
▸ LMNA P02545 1/20 0.63
▸ MEN1 O00255 2/20 0.58
▸ KMT2A Q03164 2/20 0.58
▸ PKM P14618 1/20 0.58
▸ SMN1; SMN2 Q16637 1/20 0.58
▸ PAX8 Q06710 1/20 0.58
▸ NOD2 Q9HC29 1/20 0.58
▸ L3MBTL1 Q9Y468 1/20 0.58
▸ TNF P01375 1/20 0.58
▸ NOD1 Q9Y239 1/20 0.58

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
SCHEMBL29928086 1.00 APP (0.63) APPRAB9ANPC1KDM4EGLA
SCHEMBL24332467 0.94 APP (0.58) APPRAB9ANPC1KDM4EGLA
SCHEMBL24332276 0.94 APP (0.58) APPRAB9ANPC1KDM4EGLA
SCHEMBL24332167 0.94 APP (0.58) APPRAB9ANPC1KDM4EGLA
SCHEMBL24332465 0.94 APP (0.58) APPRAB9ANPC1KDM4EGLA
SCHEMBL24331811 0.93 APP (0.57) APPRAB9ANPC1KDM4EGLA
SCHEMBL24332090 0.93 APP (0.57) APPRAB9ANPC1KDM4EGLA
SCHEMBL24037899 0.91 APP (0.56) APPRAB9ANPC1KDM4EGLA
SCHEMBL24037844 0.91 APP (0.56) APPRAB9ANPC1KDM4EGLA
SCHEMBL11448605 0.91 APP (0.54) APPRAB9ANPC1KDM4EGLA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104761536-B Method of synthesizing 2-substituted benzothiazole-type derivative 内蒙古工业大学 2017-05-10 — — CN claimed
CN-104761536-A Method of synthesizing 2-substituted benzothiazole-type derivative UNIV INNER MONGOLIA TECHNOLOGY 2015-07-08 — — CN claimed
CN-115197165-B Method for preparing benzothiazole compound by reacting photocatalytic toluene compound and o-aminophenylsulfiol 河南师范大学 2024-01-26 — — CN disclosed
CN-115057830-B Method for synthesizing 2-aryl benzothiazole 辽宁科技大学 2023-08-18 — — CN disclosed
CN-116422347-A Preparation method and application of QDs/TNTs composite catalyst material 浙江理工大学 2023-07-14 — — CN disclosed
CN-115197165-A Method for preparing benzothiazole compound by photocatalytic reaction of toluene compound and o-aminothiophenol 河南师范大学 2022-10-18 — — CN disclosed
CN-109180590-A A method of Benzoheterocyclic compounds are quickly prepared using physical grinding method under room temperature solvent-free 福建医科大学 2019-01-11 — — CN disclosed
CN-105884714-B A kind of green syt 2- replaces the method for benzo thiazole derivative 内蒙古工业大学 2018-11-23 — — CN disclosed
CN-104761536-B Method of synthesizing 2-substituted benzothiazole-type derivative 内蒙古工业大学 2017-05-10 — — CN disclosed
CN-105884714-A Method for realizing green synthesis of 2-substituted benzothiazole derivatives 内蒙古工业大学 2016-08-24 — — CN disclosed
CN-103408505-B A kind of is the method that Material synthesis 2-replaces benzo thiazole derivative with carboxylic acid and disulphide NEI MONGOL POLYTECHNICAL UNIV. (CN) 2015-11-25 — — CN disclosed
CN-104761536-A Method of synthesizing 2-substituted benzothiazole-type derivative UNIV INNER MONGOLIA TECHNOLOGY 2015-07-08 — — CN disclosed
CN-103408505-A Method for synthesizing 2-substituted benzothiazole derivative by adopting carboxylic acid and disulfide as raw materials UNIV INNER MONGOLIA TECHNOLOGY 2013-11-27 — — CN disclosed
CN-1325503-C Luminous organic intermetallic compound and luminous element SANYO ELECTRIC CO (JP) 2007-07-11 — — CN disclosed
EP-0763532-B1 Liquid crystalline compound and use thereof DAINIPPON PRINTING CO LTD (JP) 2004-08-11 — — EP disclosed
CN-1397559-A Luminous organic intermetallic compound and luminous element SANYO ELECTRIC CO (JP) 2003-02-19 — — CN disclosed
US-5980779-A REACTING AN ACTIVATED 4-SUBSTITUTED BENZENE WITH AN ACTIVATED 5-SUBSTITUTED BENZOTHIAZOLE TO OBTAIN 2-((4-SUBSTITUTED PHENYL)-Z-),5-SUBSTITUTED BENZOTHIAZOLE WHERE Z IS AN ESTER, AZO, IMINE, SULFIDE, CARBON CARBON DOUBLE OR TRIPLE BOND DAI NIPPON PRINTING CO., LTD. (JP) 1999-11-09 — — US disclosed
US-5766510-A REACTING TWO MOLES OF SUBSTITUTED BENZOIC ACID OR BENZALDEHYDE WITH ONE MOLE OF 1,3-DIAMINO-4,6-DIMERCAPTOBENZENE TO FORM LIQUID CRYSTALLINE COMPOUND DAI NIPPON PRINTING CO., LTD. (JP) 1998-06-16 — — US disclosed
EP-0763532-A2 Liquid crystalline compound and use thereof DAI NIPPON PRINTING CO., LTD. (JP) 1997-03-19 — — EP disclosed
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