SCHEMBL2868747

SCHEMBL2868747

Cc1cc(-c2ccc(N=Nc3cc(S(=O)(=O)[O-])c4ccccc4c3N)c(C)c2)ccc1N=Nc1cc(S(=O)(=O)[O-])c2ccccc2c1N.[Na+].[Na+]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
▸ THRB known ✓ P10828 1/20 1.00
▸ ALDH1A1 P00352 1/20 1.00
▸ CYP3A4 P08684 1/20 1.00
▸ HPGD P15428 1/20 1.00
▸ ALOX15 P16050 1/20 1.00
▸ TSHR P16473 1/20 1.00
▸ ALOX12 P18054 1/20 1.00
▸ MAPK1 P28482 1/20 1.00
▸ RECQL P46063 1/20 1.00
▸ HSD17B10 Q99714 1/20 1.00
▸ ENPP2 Q13822 3/20 0.71
▸ APP P05067 1/20 0.71
▸ GLB1 P16278 1/20 0.71
▸ CHAT P28329 1/20 0.71
▸ PHLPP2 Q6ZVD8 1/20 0.71
▸ CTRC Q99895 1/20 0.71
▸ ALB P02768 1/20 0.61
▸ HSPD1 P10809 1/20 0.61
▸ PTPN1 P18031 1/20 0.61
▸ HSPE1 P61604 1/20 0.61

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
SCHEMBL1897261 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4THRBHPGDALOX15
SCHEMBL29362889 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4THRBHPGDALOX15
SCHEMBL23787656 0.87 ALDH1A1 (0.77) ALDH1A1CYP3A4THRBHPGDALOX15
SCHEMBL11922531 0.86 SENP2 (0.79) ALDH1A1CYP3A4THRBHPGDALOX15
SCHEMBL19154084 0.86 SENP2 (0.79) ALDH1A1CYP3A4THRBHPGDALOX15
SCHEMBL29382082 0.85 THRB (0.74) ALDH1A1CYP3A4THRBHPGDALOX15
Congo Red Free Acid SCHEMBL29395841 0.83 APP (1.00) ALDH1A1CYP3A4THRBHPGDALOX15
Congo Red Free Acid SCHEMBL29366109 0.83 APP (1.00) ALDH1A1CYP3A4THRBHPGDALOX15
Congo Red Free Acid SCHEMBL25635 0.83 APP (1.00) ALDH1A1CYP3A4THRBHPGDALOX15
Congo Red Free Acid SCHEMBL202229 0.83 APP (1.00) ALDH1A1CYP3A4THRBHPGDALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009134794-A1 MATERIALS AND METHODS FOR CREATING CUSTOMIZED COMPOSITIONS HAVING A TEMPORARY VISUAL INDICATOR MELKER RICHARD J (US) 2009-11-05 — — WO claimed
CN-114796235-A Application of taurocholic acid and water-soluble salt thereof in inhibiting activity of endoribonuclease of new coronavirus 华中科技大学 2022-07-29 — — CN disclosed
US-10589003-B2 Methods for coating surfaces with antimicrobial agents THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2020-03-17 — — US disclosed
US-20180303977-A1 METHODS FOR COATING SURFACES WITH ANTIMICROBIAL AGENTS THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2018-10-25 — — US disclosed
US-7713472-B2 Antiseptic derivatives with broad spectrum antimicrobial activity for the impregnation of surfaces BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2010-05-11 — — US disclosed
US-7651661-B2 Medical devices with broad spectrum antimicrobial activity BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2010-01-26 — — US disclosed
WO-2009134794-A1 MATERIALS AND METHODS FOR CREATING CUSTOMIZED COMPOSITIONS HAVING A TEMPORARY VISUAL INDICATOR MELKER RICHARD J (US) 2009-11-05 — — WO disclosed
US-20080227856-A1 Materials and Methods for Creating Customized Compositions Having a Temporary Visual Indicator MELKER RICHARD J 2008-09-18 — — US disclosed
US-20080183152-A1 MEDICAL DEVICES WITH BROAD SPECTRUM ANTIMICROBIAL ACTIVITY RAAD ISSAM 2008-07-31 — — US disclosed
US-7261857-B2 Colorimetric artificial nose having an array of dyes and method for artificial olfaction THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2007-08-28 — — US disclosed
US-20070154621-A1 METHODS FOR COATING SURFACES WITH ANTIMICROBIAL AGENTS THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM 2007-07-05 — — US disclosed
US-20050197634-A1 Methods for coating and impregnating medical devices with antiseptic compositions BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM 2005-09-08 — — US disclosed
US-20030166298-A1 Colorimetric artificial nose having an array of dyes and method for artificial olfaction BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2003-09-04 — — US disclosed
US-20030143112-A1 Colorimetric artificial nose having an array of dyes and method for artificial olfaction BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2003-07-31 — — US disclosed
US-20030113923-A1 Steam-formaldehyde sterilization process indicator inks ILLINOIS TOOL WORKS INC. 2003-06-19 — — US 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 (2 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-10589003-B2 Methods for coating surfaces with antimicrobial agents CUTA, CD63, CDC37 THRB 4713/4885ALDH1A1 1120/4885CYP3A4 1574/4885
US-20180303977-A1 METHODS FOR COATING SURFACES WITH ANTIMICROBIAL AGENTS CUTA, CD63, CDC37 THRB 4713/4885ALDH1A1 1120/4885CYP3A4 1574/4885

“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.

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