SCHEMBL925266

SCHEMBL925266

O=C([O-])c1cc(/N=N/c2cccc([N+](=O)[O-])c2)ccc1O.[Na+]

nearest known ligand 0.60

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE4A known ✓ P27815 1/20 0.46
ALDH1A1 P00352 8/20 0.59
TDP1 Q9NUW8 2/20 0.59
SMN1; SMN2 Q16637 1/20 0.59
MAPT P10636 3/20 0.48
MAPK1 P28482 2/20 0.48
L3MBTL1 Q9Y468 2/20 0.48
LMNA P02545 1/20 0.48
PKM P14618 1/20 0.48
BLM P54132 1/20 0.48
MCL1 Q07820 1/20 0.48
NPSR1 Q6W5P4 1/20 0.48
NLRP3 Q96P20 1/20 0.48
IDO1 P14902 1/20 0.48
MEN1 O00255 6/20 0.46
KMT2A Q03164 6/20 0.46
BLVRB P30043 1/20 0.46
KDR P35968 1/20 0.46
HTT P42858 1/20 0.46
CCNT1 O60563 1/20 0.44

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
SCHEMBL2384122 1.00 ALDH1A1 (0.59) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL2384129 0.89 ALDH1A1 (0.75) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL4047509 0.88 ALDH1A1 (0.77) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL29481568 0.88 ALDH1A1 (0.77) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL4051923 0.88 ALDH1A1 (0.77) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL264266 0.87 ALDH1A1 (0.76) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL7033976 0.87 ALDH1A1 (0.76) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL2384120 0.86 ALDH1A1 (0.75) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
SCHEMBL2384124 0.86 ALDH1A1 (0.75) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1
Olsalazine SCHEMBL3476110 0.82 MEN1 (0.66) ALDH1A1TDP1SMN1; SMN2MAPTMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122070479-A Ultrasonic indicating device and method for monitoring ultrasonic treatment JP实验室股份有限公司 2026-05-19 CN claimed
WO-2025090061-A1 ULTRASONIC INDICATOR DEVICE AND METHOD FOR MONITORING ULTRASONICATION JP LABORATORIES, INC. (US) 2025-05-01 WO claimed
WO-2025075611-A1 ULTRASONIC INDICATOR BASED ON EMULSION FORMATION JP LABORATORIES, INC. (US) 2025-04-10 WO claimed
US-20210256870-A1 COLOR CHANGING MICTURITION TRAINING COMPOSITION AND PROCESS FOR USE THEREOF POTTY MAGIC LLC (US) 2021-08-19 US claimed
EP-2900281-B1 LIQUID ACTIVATED COLOR CHANGE INK AND METHODS OF USE PROCTER & GAMBLE (US) 2019-09-18 EP claimed
WO-2019161190-A1 HYDROCHROMIC COATINGS AND RELATED METHODS CHROMATIC TECHNOLOGIES, INC. (US) 2019-08-22 WO claimed
CN-108103582-A A kind of low-temp reversible thermochromic crystals material, preparation method and the usage 江南大学 2018-06-01 CN claimed
US-9726613-B2 Liquid activated color change ink and methods of use THE PROCTER & GAMBLE COMPANY (US) 2017-08-08 US claimed
EP-3177250-A1 WETNESS INDICATOR WITH PERMANENT COLORANT The Procter and Gamble Company (US) 2017-06-14 EP claimed
US-20160282276-A1 LIQUID ACTIVATED COLOR CHANGE INK AND METHODS OF USE PROCTER & GAMBLE (US) 2016-09-29 US claimed
US-20090275908-A1 Absorbent Articles Capable of Indicating the Presence of Urine KIMBERLY-CLARK WORLDWIDE, INC. (US) 2009-11-05 US claimed
WO-2009133480-A2 ABSORBENT ARTICLES CAPABLE OF INDICATING THE PRESENCE OF URINE KIMBERLY-CLARK WORLDWIDE, INC. (US) 2009-11-05 WO claimed
WO-2009033135-A1 UNIVERSAL DRINKING ADAPTER FOR BEVERAGE BOTTLES TO ALLOW FOR LIQUID CONSUMPTION AND DEVICES AND KITS FOR DETERMINING SMALL MOLECULES, METAL IONS, ENDOTOXINS, AND BACTERIA FOUND IN MILK, AND METHODS OF USE THEREOF SUREMILK, LLC. (US) 2009-03-12 WO claimed
EP-1954391-A2 ADSORBENT COMPOSITION WITH REACTIVE INDICATOR PURAFIL, INC. (US) 2008-08-13 EP claimed
WO-2007047557-A2 ADSORBENT COMPOSITION WITH REACTIVE INDICATOR PURAFIL, INC. (US) 2007-04-26 WO claimed
US-20070087444-A1 Adsorbent composition with reactive indicator PURAFIL, INC. 2007-04-19 US claimed
CN-1273550-C Aluminium salt bottoming acidic medium dye digitial printing ink and printing method of digital printing ink BEIJING GARMENT COLLEGE (CN) 2006-09-06 CN claimed
CN-1511896-A Aluminium salt bottoming acidic medium dye digitial printing ink and printing method of digital printing ink 北京服装学院 2004-07-14 CN claimed
US-6617123-B1 Contacting sample with mixture of an esterase, a pH indicator dye and a buffer; colorimetric analysis; easy, convenient test strips SMITH JACK V (US) 2003-09-09 US claimed
US-5914806-A Stable electrophoretic particles for displays INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 1999-06-22 US claimed