SCHEMBL7129526

SCHEMBL7129526

COc1ccc(C(=O)c2ccc(OC)c(S(=O)(=O)[O-])c2O)c(O)c1.[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
ADORA3 known ✓ P0DMS8 1/20 0.53
PDE4A known ✓ P27815 1/20 0.49
PDE4D known ✓ Q08499 1/20 0.49
NPC1 O15118 3/20 0.60
RAB9A P51151 2/20 0.60
HPGD P15428 5/20 0.53
LMNA P02545 5/20 0.53
CYP3A4 P08684 4/20 0.53
CYP2C19 P33261 3/20 0.53
CYP1A2 P05177 2/20 0.53
PGR P06401 2/20 0.53
SLC6A2 P23975 2/20 0.53
AR P10275 1/20 0.53
CHRM1 P11229 1/20 0.53
ALOX15 P16050 1/20 0.53
TBXA2R P21731 1/20 0.53
ADRA1A P35348 1/20 0.53
HIF1A Q16665 1/20 0.53
MAPK1 P28482 5/20 0.49
ALDH1A1 P00352 5/20 0.49

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
SCHEMBL9363053 0.88 MAPT (0.46) NPC1RAB9AHPGDLMNACYP3A4
SCHEMBL8427070 0.87 NPC1 (0.63) NPC1RAB9AHPGDLMNACYP3A4
SCHEMBL7129528 0.86 NPC1 (0.61) NPC1RAB9AHPGDLMNACYP3A4
SCHEMBL1274132 0.81 NPC1 (0.61) NPC1RAB9AHPGDLMNACYP3A4
Lithium Ion SCHEMBL10491553 0.79 NPC1 (0.61) NPC1RAB9AHPGDLMNACYP3A4
Potassium Ion SCHEMBL10491864 0.79 NPC1 (0.61) NPC1RAB9AHPGDLMNACYP3A4
SCHEMBL9762530 0.78 NPC1 (0.65) NPC1RAB9AHPGDLMNACYP3A4
SCHEMBL170073 0.78 MAPT (0.65) RAB9AHPGDLMNACYP3A4CYP2C19
SCHEMBL7332618 0.78 RAB9A (0.80) NPC1RAB9AHPGDLMNACYP3A4
Sulfuric Acid SCHEMBL9740504 0.78 NPC1 (0.86) NPC1RAB9AHPGDLMNACYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6579826-B2 Having a crosslinked polymer layer including an ultraviolet absorbing structure, e.g. containing a benzotriaxole moiety; protective coatings; durability; using a coloring reaction of an electron donating leuko dye with an electron acceptor RICOH COMPANY LIMITED (JP) 2003-06-17 US disclosed
US-6524377-B2 Phenolic electron accepting color developer and electron donating coloring agent such as leuco dye; achieves color on heating; erasure on cooling; durability; reusable RICOH COMPANY, LTD. (JP) 2003-02-25 US disclosed
US-6503868-B2 Phenolic electron accepting color developer and electron donating coloring agent; leuco dye; achieves color on heating; erasure on cooling; durability; reusable RICOH COMPANY, LTD. (JP) 2003-01-07 US disclosed
US-6410478-B1 A LAYER COMPRISING COLORING AGENT(LEUCO DYE), COLOR DEVELOPERS AND DECOLORING PROMOTERS COATED ON A SUPPORT; IMAGE DISPLAYS AND AS A REWRITABLE PAPER RICOH COMPANY, LTD. (JP) 2002-06-25 US disclosed
US-20020072472-A1 Reversible thermosensitive recording medium and image forming and erasing method using the recording medium RICOH COMPANY LIMITED (JP) 2002-06-13 US disclosed
US-20010039243-A1 Reversible thermosensitive coloring composition and recording material using the composition and recording method using the recording material TORII MASAFUMI (JP) 2001-11-08 US disclosed
US-20010025587-A1 Reversible thermosensitive coloring composition and recording material using the composition and recording method using the recording material TORII MASAFUMI (JP) 2001-10-04 US disclosed
US-6207613-B1 ELECTRON ACCEPTING COLOR DEVELOPER INCLUDES A PHENOLIC COMPOUND RICOH COMPANY, LTD. (JP) 2001-03-27 US disclosed
US-5981429-A AN ELECTRON-DONATING COLORING COMPOUND (COLORING AGENT) AND AN ELECTRON-ACCEPTING COMPOUND (DEVELOPER), CAPABLE OF INDUCING COLOR FORMATION BY REACTING BOTH COMPOUNDS, AND EARSING THE COLOR BY CONTROLLING HEAT ENERGY RICOH COMPANY, LTD. (JP) 1999-11-09 US disclosed