SCHEMBL29362889

SCHEMBL29362889

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
SCHEMBL2868747 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 198 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114867351-B 4' -Halogen-containing nucleotide and nucleoside therapeutic compositions and related uses 埃默里大学 2024-04-23 — — CN claimed
US-11795340-B2 Compositon sensitive to UV-C radiation and UV-C sterilization or disinfection dosimeter TERRAGENE S.A. (AR) 2023-10-24 — — US claimed
CN-114867351-A 4' -halo-containing nucleotide and nucleoside therapeutic compositions and uses related thereto 埃默里大学 2022-08-05 — — CN claimed
EP-3964554-A1 COMPOSITON SENSITIVE TO UV-C RADIATION AND UV-C STERILIZATION OR DISINFECTION DOSIMETER Terragene LLC (US) 2022-03-09 — — EP claimed
EP-4743588-A2 TREATMENT OF SAMPLES CONTAINING NUCLEIC ACIDS BioSpyder Technologies, Inc. (US) 2026-05-20 — — EP disclosed
US-12607931-B2 Photosensitive transfer material, light shielding material, LED array, and electronic apparatus FUJIFILM CORPORATION (JP) 2026-04-21 — — US disclosed
EP-4714452-A1 METHODS FOR TREATING SARS COV-2 INFECTIONS Gilead Sciences, Inc. (US) 2026-03-25 — — EP disclosed
EP-3958047-B1 OPTICAL MATERIAL MITSUI CHEMICALS INC (JP) 2026-03-04 — — EP disclosed
EP-4701454-A1 WRAPPER WITH PH INDICATOR FOR AEROSOL-GENERATING ARTICLE Philip Morris Products S.A. (CH) 2026-03-04 — — EP disclosed
US-12552745-B2 Compound for optical materials, curable composition, cured body, and optical article TOKUYAMA CORPORATION (JP) 2026-02-17 — — US disclosed
US-20250355282-A1 LAYERED BODY, OPTICAL ARTICLE, LENS, AND SPECTACLES TOKUYAMA CORPORATION (JP) 2025-11-20 — — US disclosed
EP-4067998-B1 EO/PO MODIFIED 9-PHENYLACRIDINE PHOTOSENSITIZERS FOR USE IN PHOTOSENSITIVE RESINS IN THE MANUFACTURE OF PRINTED CIRCUIT BOARDS CHANGZHOU TRONLY NEW ELECTRONIC MAT CO LTD (CN) 2025-11-12 — — EP disclosed
WO-2022045203-A1 TRANSFER FILM, MANUFACTURING METHOD FOR LAMINATE, AND MANUFACTURING METHOD FOR CIRCUIT WIRING 富士フイルム株式会社 2022-03-03 — — WO disclosed
CN-114096899-A Polarizing film and method for producing same 株式会社可乐丽 2022-02-25 — — CN disclosed
EP-3958044-A1 OPTICAL MATERIAL, POLYMERIZABLE COMPOSITION FOR OPTICAL MATERIAL, CURED PRODUCT, OPTICAL MATERIAL, PLASTIC LENS, METHOD FOR MANUFACTURING OPTICAL MATERIAL, AND METHOD FOR USING OPTICAL MATERIAL Mitsui Chemicals, Inc. (JP) 2022-02-23 — — EP disclosed
EP-3958047-A1 OPTICAL MATERIAL Mitsui Chemicals, Inc. (JP) 2022-02-23 — — EP disclosed
EP-3951443-A1 METHOD FOR PRODUCING OPTICAL MATERIAL, AND POLYMERIZABLE COMPOSITION FOR OPTICAL MATERIAL Mitsui Chemicals, Inc. (JP) 2022-02-09 — — EP disclosed
CN-114026199-A Polarizing luminescent film, polarizing luminescent sheet, and display device containing water-soluble coumarin compound or salt thereof 日本化药株式会社 2022-02-08 — — CN disclosed
CN-114008497-A Polarizing film and method for producing same 株式会社可乐丽 2022-02-01 — — CN disclosed
WO-2022019321-A1 COMPOSITION, TRANSFER FILM, METHOD FOR PRODUCING LAMINATE, METHOD FOR PRODUCING CIRCUIT WIRING, AND METHOD FOR PRODUCING ELECTRONIC DEVICE 富士フイルム株式会社 2022-01-27 — — 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 (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-12607931-B2 Photosensitive transfer material, light shielding material, LED array, and electronic apparatus SETD1B, NLRP1, MAP1LC3B THRB 2370/4885ALDH1A1 1082/4885CYP3A4 3299/4885
US-12552745-B2 Compound for optical materials, curable composition, cured body, and optical article C5, SCO2, ZYX THRB 2158/4885ALDH1A1 1308/4885CYP3A4 2189/4885

“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.

Send feedback