SCHEMBL19953365

SCHEMBL19953365

O=S(=O)([O-])c1ccc(S(=O)(=O)[O-])cc1.[Na+].[Na+]

nearest known ligand 0.55

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
CA12 known ✓ O43570 2/20 0.38
CA2 known ✓ P00918 2/20 0.38
CA1 known ✓ P00915 1/20 0.36
CA4 known ✓ P22748 1/20 0.36
LMNA P02545 3/20 0.55
TDP1 Q9NUW8 2/20 0.55
DUSP5 Q16690 3/20 0.44
PTPN1 P18031 2/20 0.44
DUSP6 Q16828 1/20 0.44
NR1I2 O75469 1/20 0.41
PLCG1 P19174 1/20 0.39
TSHR P16473 3/20 0.38
CYP3A4 P08684 2/20 0.38
ALDH1A1 P00352 2/20 0.38
CA9 Q16790 2/20 0.38
MAPK1 P28482 1/20 0.38
MPO P05164 1/20 0.38
CYP2C9 P11712 1/20 0.38
HTR6 P50406 1/20 0.38
GAA P10253 1/20 0.38

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
Potassium Ion SCHEMBL1538011 0.92 LMNA (0.48) LMNATDP1DUSP5PTPN1DUSP6
SCHEMBL28934944 0.92 LMNA (0.48) LMNATDP1DUSP5PTPN1DUSP6
SCHEMBL5846996 0.90 CA12 (0.52) LMNATDP1DUSP5PTPN1DUSP6
SCHEMBL3171668 0.90 CA12 (0.52) LMNATDP1DUSP5PTPN1DUSP6
SCHEMBL28477667 0.87 HTR6 (0.55) LMNATDP1TSHRALDH1A1CA12
SCHEMBL3409456 0.87 HTR6 (0.55) LMNATDP1TSHRALDH1A1CA12
SCHEMBL28929 0.87 HTR6 (0.55) LMNATDP1TSHRALDH1A1CA12
SCHEMBL1981609 0.87 HTR6 (0.55) LMNATDP1TSHRALDH1A1CA12
SCHEMBL6740023 0.87 HTR6 (0.55) LMNATDP1TSHRALDH1A1CA12
SCHEMBL11761400 0.87 HTR6 (0.55) LMNATDP1TSHRALDH1A1CA12

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
EP-4302082-B1 ASSEMBLY COMPRISING A WINDOW PANE WITH AT LEAST ONE CAPACITIVE HUMIDITY SENSOR AND ELECTRONIC PROCESSING MEANS SAINT GOBAIN SEKURIT FRANCE (FR) 2026-04-15 EP claimed
US-20250270168-A1 SYNTHESIS PROCESS FOR HIGH PURITY ISOSULFAN BLUE USING FLASH CHROMATOGRAPHY IN COMMERCIAL PLANT SCALE RISING PHARMA HOLDINGS, INC. (US) 2025-08-28 US claimed
US-12180142-B1 Synthesis process for high purity isosulfan blue using flash chromatography in commercial plant scale RISING PHARMA HOLDINGS, INC. (US) 2024-12-31 US claimed
EP-4302082-A1 GLAZING PROVIDED WITH A CAPACITIVE HUMIDITY SENSOR Saint-Gobain Glass France (FR) 2024-01-10 EP claimed
WO-2022184988-A1 GLAZING PROVIDED WITH A CAPACITIVE HUMIDITY SENSOR SAINT-GOBAIN GLASS FRANCE (FR) 2022-09-09 WO claimed
WO-2018046930-A1 PROCESS FOR THE PREPARATION OF ZIRCONIUM BASED MOFS. UNIVERSITETET I OSLO (NO) 2018-03-15 WO claimed
US-20250270168-A1 SYNTHESIS PROCESS FOR HIGH PURITY ISOSULFAN BLUE USING FLASH CHROMATOGRAPHY IN COMMERCIAL PLANT SCALE RISING PHARMA HOLDINGS, INC. (US) 2025-08-28 US disclosed
US-12180142-B1 Synthesis process for high purity isosulfan blue using flash chromatography in commercial plant scale RISING PHARMA HOLDINGS, INC. (US) 2024-12-31 US disclosed
CN-118851949-A Synthesis method of triarylmethane sulfone compound 普如制药生命解决方案公司 2024-10-29 CN disclosed
CN-115551830-B Synthesis method of triarylmethane sulfone compound 普如制药生命解决方案公司 2024-09-06 CN disclosed
CN-115485264-B Synthesis method of triarylmethane sulfone compound 普如制药生命解决方案公司 2024-07-19 CN disclosed
EP-4302082-A1 GLAZING PROVIDED WITH A CAPACITIVE HUMIDITY SENSOR Saint-Gobain Glass France (FR) 2024-01-10 EP disclosed
CN-115551830-A Synthesis method of triarylmethane sulfone compound 普如制药生命解决方案公司 2022-12-30 CN disclosed
CN-115485264-A Method for synthesizing triarylmethane sulfone compound 普如制药生命解决方案公司 2022-12-16 CN disclosed
WO-2022184988-A1 GLAZING PROVIDED WITH A CAPACITIVE HUMIDITY SENSOR SAINT-GOBAIN GLASS FRANCE (FR) 2022-09-09 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-20250270168-A1 SYNTHESIS PROCESS FOR HIGH PURITY ISOSULFAN BLUE USING FLASH CHROMATOGRAPHY IN COMMERCIAL PLANT SCALE CBS, SLC6A12, RPS4Y1 CA12 801/4885CA2 185/4885CA1 2130/4885
US-12180142-B1 Synthesis process for high purity isosulfan blue using flash chromatography in commercial plant scale CBS, SLC6A12, RPS4Y1 CA12 801/4885CA2 185/4885CA1 2130/4885

“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.