SCHEMBL2090795

SCHEMBL2090795

COc1cccc(-c2nc3ccccc3s2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 8/20 1.00
SMN1; SMN2 Q16637 7/20 1.00
RAB9A P51151 6/20 1.00
NFKB1 P19838 3/20 1.00
NFKB2 Q00653 3/20 1.00
RELA Q04206 3/20 1.00
TDP1 Q9NUW8 2/20 1.00
KDM4E B2RXH2 5/20 0.78
ALDH1A1 P00352 4/20 0.78
MEN1 O00255 3/20 0.78
KMT2A Q03164 3/20 0.78
HPGD P15428 3/20 0.78
L3MBTL1 Q9Y468 1/20 0.78
NPC1 O15118 3/20 0.70
PKM P14618 1/20 0.70
TP53 P04637 4/20 0.61
LMNA P02545 3/20 0.61
HSD17B10 Q99714 2/20 0.61
POLB P06746 1/20 0.61
GLA P06280 1/20 0.60

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
SCHEMBL30161523 1.00 MAPT (1.00) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL5421230 0.88 SMN1; SMN2 (0.78) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL2090792 0.85 RAB9A (0.74) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL7619684 0.84 MAPT (0.72) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL5461064 0.84 RAB9A (0.77) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL3190375 0.83 MAPT (0.71) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL2242816 0.83 KDM4E (1.00) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL12687369 0.82 MAPT (0.69) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL14742583 0.82 MAPT (0.69) MAPTSMN1; SMN2RAB9ANFKB1NFKB2
SCHEMBL6204792 0.81 SMN1; SMN2 (0.81) MAPTSMN1; SMN2RAB9ANFKB1NFKB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118047723-A Process for preparing benzoazacyclic compounds 常州大学 2024-05-17 CN disclosed
CN-115739190-B Metal complex catalyst for phytic acid and preparation method and application thereof 江南大学 2024-02-13 CN disclosed
CN-115057830-B Method for synthesizing 2-aryl benzothiazole 辽宁科技大学 2023-08-18 CN disclosed
CN-115739190-A Phytic acid metal complex catalyst and preparation method and application thereof 江南大学 2023-03-07 CN disclosed
CN-111793040-B Preparation method of 2-substituted benzothiazole 太原理工大学 2023-01-03 CN disclosed
CN-111793040-A Preparation method of 2-substituted benzothiazole 太原理工大学 2020-10-20 CN disclosed
WO-2019144845-A1 SPIRO-CONTAINING PLATINUM (II) EMITTERS WITH TUNABLE EMISSION ENERGIES AND SYNTHESES THEREOF THE UNIVERSITY OF HONG KONG (CN) 2019-08-01 WO disclosed
CN-105859652-B Yb/MCM-41 molecular sieve catalyst catalyzes and synthesizes the method that 2- replaces benzothiazole compound 同济大学 2019-03-01 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
EP-3251694-A1 DRUG COMBINATIONS FOR THE TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY Summit (Oxford) Limited (GB) 2017-12-06 EP disclosed
US-8518980-B2 Treatment of Duchenne muscular dystrophy SUMMIT CORPORATION PLC (GB) 2013-08-27 US disclosed
US-8501713-B2 Drug combinations for the treatment of duchenne muscular dystrophy SUMMIT CORPORATION PLC (GB) 2013-08-06 US disclosed
CN-103073520-A Method for synthesizing 2-phenyl benzothiazole and derivative thereof UNIV HUNAN 2013-05-01 CN disclosed
US-8163753-B2 2-(4-(4-(4-chlorophenyl)oxazol-2-yl)phenoxymethyl)-2-methyl-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole; bactericide; excellent bactericidal action against Mycobacterium tuberculosis, multi-drug-resistant Mycobacterium tuberculosis, and atypical acid-fast bacteria OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2012-04-24 US disclosed
US-20110195932-A1 Drug Combinations for the Treatment of Duchenne Muscular Dystrophy SUMMIT (OXFORD) LIMITED (GB) 2011-08-11 US disclosed
US-20090075938-A1 TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY SUMMIT (OXFORD) LIMITED (GB) 2009-03-19 US disclosed
EP-1986633-A2 TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY Summit Corporation Plc (GB) 2008-11-05 EP disclosed
EP-1678185-B1 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMA CO LTD (JP) 2008-10-08 EP disclosed
US-20080119478-A1 2,3-Dihydro-6-Nitroimidazo (2,1-b) Oxazole Compounds for the Treatment of Tuberculosis OTSUKA PHAMACEUTICAL CO., LTD. (JP) 2008-05-22 US disclosed
WO-2007091106-A2 TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY SUMMIT CORPORATION PLC (GB) 2007-08-16 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110195932-A1 Drug Combinations for the Treatment of Duchenne Muscular Dystrophy PYGM, CPT1B, GYS1 MAPT 3113/4885SMN1; SMN2 4/4885RAB9A 3748/4885
US-20080119478-A1 2,3-Dihydro-6-Nitroimidazo (2,1-b) Oxazole Compounds for the Treatment of Tuberculosis NR2C2, NR0B2, NR4A2 MAPT 4299/4885SMN1; SMN2 3787/4885RAB9A 3153/4885
US-20090075938-A1 TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY NR0B1, NR0B2, NR3C1 MAPT 4858/4885SMN1; SMN2 9/4885RAB9A 4325/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.