SCHEMBL2394479

SCHEMBL2394479

Nc1ccc(/N=N/c2ccc(S(=O)(=O)O)cc2)cc1.[NaH]

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.72
ALDH1A1 P00352 1/20 0.72
NT5E P21589 1/20 0.72
CA2 P00918 5/20 0.66
CA12 O43570 4/20 0.66
CA9 Q16790 4/20 0.66
POLB P06746 1/20 0.66
CYP2D6 P10635 1/20 0.66
MAPT P10636 3/20 0.56
RAB9A P51151 3/20 0.56
MEN1 O00255 3/20 0.56
KMT2A Q03164 3/20 0.56
NPC1 O15118 2/20 0.56
TDP1 Q9NUW8 2/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
L3MBTL1 Q9Y468 1/20 0.56
RPS6KA3 P51812 1/20 0.50
SUMO2 P61956 1/20 0.49
SUMO1 P63165 1/20 0.49
SENP7 Q9BQF6 1/20 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
SCHEMBL11590196 1.00 TSHR (0.72) TSHRALDH1A1NT5ECA2CA12
SCHEMBL5752505 0.98 TSHR (0.75) TSHRALDH1A1NT5ECA2CA12
SCHEMBL1485997 0.98 TSHR (0.75) TSHRALDH1A1NT5ECA2CA12
SCHEMBL28543329 0.96 TSHR (0.72) TSHRALDH1A1NT5ECA2CA12
SCHEMBL18624977 0.87 POLB (0.83) TSHRALDH1A1NT5ECA2CA12
SCHEMBL28560987 0.87 POLB (0.83) TSHRALDH1A1NT5ECA2CA12
SCHEMBL646074 0.87 TSHR (0.95) TSHRALDH1A1NT5ECA2CA12
SCHEMBL7766917 0.87 TSHR (0.95) TSHRALDH1A1NT5ECA2CA12
Water SCHEMBL2045998 0.85 TSHR (0.90) TSHRALDH1A1NT5ECA2CA12
SCHEMBL28275690 0.85 TSHR (0.90) TSHRALDH1A1NT5ECA2CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111187408-A Method for synthesizing polyamino acid with photoresponse characteristic 金陵科技学院 2020-05-22 CN claimed
EP-1515144-B2 METHOD OF ASSAY WITH SULFONIC ACID COMPOUND AND NITRO COMPOUND ARKRAY INC (JP) 2013-04-24 EP claimed
US-8021855-B2 Method of decomposing protein with sulfonic acid compound ARKRAY INC. (JP) 2011-09-20 US claimed
EP-1515144-B1 METHOD OF ASSAY WITH SULFONIC ACID COMPOUND AND NITRO COMPOUND ARKRAY INC (JP) 2009-10-14 EP claimed
US-7354732-B2 Method of assay with sulfonic acid compound and nitro compound ARKRAY, INC. (JP) 2008-04-08 US claimed
US-20050260735-A1 Method of decomposing protein with sulfonic acid compound ARKRAY, INC. (JP) 2005-11-24 US claimed
US-20050221415-A1 Method of assay with sulfonic acid compound and nitro compound ARKRAY, INC. (JP) 2005-10-06 US claimed
EP-1522593-A1 METHOD OF DECOMPOSING PROTEIN WITH SULFONIC ACID COMPOUND ARKRAY, Inc. (JP) 2005-04-13 EP claimed
EP-1515144-A1 METHOD OF ASSAY WITH SULFONIC ACID COMPOUND AND NITRO COMPOUND ARKRAY, Inc. (JP) 2005-03-16 EP claimed
JP-4293969-A None JP disclosed
US-20250221408-A1 COMPOSITION EARTH CORPORATION (JP) 2025-07-10 US disclosed
EP-3550030-B1 METHOD FOR MEASURING GLYCATION RATE OF HEMOGLOBIN TOYO BOSEKI (JP) 2025-01-01 EP disclosed
EP-4473837-A1 COMPOSITION Earth Corporation (JP) 2024-12-11 EP disclosed
US-20240000084-A1 ANTIPATHOGENIC AGENT, ANTIBACTERIAL AGENT, ANTIVIRAL AGENT, PATHOGEN DISPOSAL DEVICE, ANTIPATHOGENIC AGENT PRODUCTION METHOD, ANTIBACTERIAL TREATMENT METHOD, VIRUS INACTIVATION METHOD, AND PATHOGEN DISPOSAL METHOD ACENET INC. (JP) 2024-01-04 US disclosed
EP-1522593-A1 METHOD OF DECOMPOSING PROTEIN WITH SULFONIC ACID COMPOUND ARKRAY, Inc. (JP) 2005-04-13 EP disclosed
EP-1515144-A1 METHOD OF ASSAY WITH SULFONIC ACID COMPOUND AND NITRO COMPOUND ARKRAY, Inc. (JP) 2005-03-16 EP disclosed
US-20020192247-A1 Thermochromic/photochromic cosmetic compositions THEISEN LYLE (US) 2002-12-19 US disclosed
JP-H04293969-A LIQUID COMPOSITION OF DIRECT DYE NIPPON KAYAKU CO LTD 1992-10-19 JP disclosed
US-4227879-A ISOLATING THE DIAZONIUM SALT OF P-(P-AMINOPHENYL)AZO BENZENESULFONIC ACID AND COUPLING WITH 6-AMINO-1-NAPHTHOL-3-SULFONIC ACID AMERICAN COLOR & CHEMICAL CORPORATION (US) 1980-10-14 US disclosed
US-4082742-A PROCESS FOR PREPARING AN AQUEOUS DISAZO DYE CONCENTRATE E. I. DU PONT DE NEMOURS AND COMPANY (US) 1978-04-04 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-20240000084-A1 ANTIPATHOGENIC AGENT, ANTIBACTERIAL AGENT, ANTIVIRAL AGENT, PATHOGEN DISPOSAL DEVICE, ANTIPATHOGENIC AGENT PRODUCTION METHOD, ANTIBACTERIAL TREATMENT METHOD, VIRUS INACTIVATION METHOD, AND PATHOGEN DISPOSAL METHOD EIF2AK2, HAO2, ZC3HAV1 TSHR 461/4885ALDH1A1 1641/4885NT5E 3141/4885
US-20250221408-A1 COMPOSITION GGPS1, PGGT1B, HBG2 TSHR 4073/4885ALDH1A1 1071/4885NT5E 4705/4885

“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.