SCHEMBL1363964

SCHEMBL1363964

O=[N+]([O-])c1ccc(S(=O)(=O)O)c([N+](=O)[O-])c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.59
MEN1 O00255 1/20 0.59
ALDH1A1 P00352 5/20 0.56
MAPK1 P28482 3/20 0.56
HIF1A Q16665 2/20 0.56
CYP1A2 P05177 2/20 0.56
CYP2C19 P33261 2/20 0.56
CYP3A4 P08684 1/20 0.56
CYP2D6 P10635 1/20 0.56
CYP2C9 P11712 1/20 0.56
GPR35 Q9HC97 3/20 0.56
TSHR P16473 2/20 0.56
TP53 P04637 1/20 0.56
HPGD P15428 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
TDP1 Q9NUW8 2/20 0.53
NT5E P21589 2/20 0.51
TXNRD1 Q16881 1/20 0.50
TXNRD3 Q86VQ6 1/20 0.50
TXNRD2 Q9NNW7 1/20 0.50

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
SCHEMBL63183 1.00 KMT2A (0.59) KMT2AMEN1ALDH1A1MAPK1HIF1A
SCHEMBL11572072 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
Water SCHEMBL7210787 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
Hydrochloric Acid SCHEMBL4449301 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
SCHEMBL3660349 0.98 KMT2A (0.61) KMT2AMEN1ALDH1A1MAPK1HIF1A
Water SCHEMBL29684003 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
SCHEMBL3148713 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
SCHEMBL11572065 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
Water SCHEMBL20573516 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A
Bromide SCHEMBL27497723 0.98 KMT2A (0.57) KMT2AMEN1ALDH1A1MAPK1HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119661858-B Activatable semiconductor polymer and preparation method and application thereof Jiageng Innovation Laboratory (CN) 2026-05-26 CN claimed
CN-122029214-A Phospholipid drug conjugate and preparation method and application thereof 上海弼领生物技术有限公司 2026-05-12 CN claimed
US-12618779-B2 Fluorescent ellman assay for free thiol detection GENENTECH, INC. (US) 2026-05-05 US claimed
EP-4663205-A1 POLYMER-DRUG CONJUGATE, INTERMEDIATE THEREOF, AND USE THEREOF Shanghai Best-Link Bioscience, LLC (CN) 2025-12-17 EP claimed
EP-4237844-B1 METHOD AND KIT FOR FLUORESCENT ELLMAN ASSAY FOR FREE THIOL DETECTION GENENTECH INC (US) 2025-10-01 EP claimed
US-20250255977-A1 EPSILON-POLY-L-LYSINE-BASED DRUG CONJUGATE, INTERMEDIATE THEREOF, AND APPLICATION THEREOF SHANGHAI BEST-LINK BIOSCIENCE, LLC (CN) 2025-08-14 US claimed
US-12357709-B2 Chemiluminescent probes for diagnostics and in vivo imaging RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2025-07-15 US claimed
CN-120137618-A Organosilicon emulsifier for oil-in-water drilling fluid and preparation method thereof 中国石油集团川庆钻探工程有限公司 2025-06-13 CN claimed
CN-119859124-A Anthraquinone organic fluorescent probe for detecting glutathione and/or ferrous ions, and preparation method and application thereof 中国药科大学 2025-04-22 CN claimed
CN-119842052-A Preparation method of light-activated CRISPR (clustered regularly interspaced short palindromic repeats) high-molecular nano-carrier for specific gene therapy 东华大学 2025-04-18 CN claimed
US-5126268-A Alcohol-ester sparation by reaction with acetate EASTMAN KODAK COMPANY (US) 1992-06-30 US claimed
EP-0474853-A1 PROTECTED HYDROXY METHOD FOR ALCOHOL-ESTER SEPARATION. EASTMAN KODAK CO (US) 1992-03-18 EP claimed
EP-0474861-A1 ALCOHOL-ESTER SEPARATION BY REACTION WITH ACETATE. EASTMAN KODAK CO (US) 1992-03-18 EP claimed
WO-1991015471-A1 PROTECTED HYDROXY METHOD FOR ALCOHOL-ESTER SEPARATION EASTMAN KODAK COMPANY (US) 1991-10-17 WO claimed
WO-1991015469-A1 ALCOHOL-ESTER SEPARATION BY REACTION WITH BICARBONATE IN POLYHYDROXY SOLVENT EASTMAN KODAK COMPANY (US) 1991-10-17 WO claimed
WO-1991015470-A1 ALCOHOL-ESTER SEPARATION BY REACTION WITH ACETATE EASTMAN KODAK COMPANY (US) 1991-10-17 WO claimed
EP-0431220-A1 Method of making a sulfonate ester and cross-linked alcohol coated support matrix UOP (US) 1991-06-12 EP claimed
US-4885207-A CROSSLINKED POLYVINYL ALCOHOL COATING ON SUPPORT MATRIX UOP (US) 1989-12-05 US claimed
US-4150055-A Reduction and desulfonation of 2,4- and 2,6- dinitrobenzenesulfonates, which may contain a methyl group in the 5-position, to primary amino compounds THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1979-04-17 US claimed
US-4063889-A Halosolvent dyeing process for polyester with cationic dyes having sulfosuccinate anions E. I. DU PONT DE NEMOURS AND COMPANY (US) 1977-12-20 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-12618779-B2 Fluorescent ellman assay for free thiol detection TST, TMT1A, AHCY KMT2A 4095/4885MEN1 4145/4885ALDH1A1 478/4885
US-12357709-B2 Chemiluminescent probes for diagnostics and in vivo imaging DAXX, DCAF15, CDY1; CDY1B KMT2A 3745/4885MEN1 2291/4885ALDH1A1 598/4885
US-20250255977-A1 EPSILON-POLY-L-LYSINE-BASED DRUG CONJUGATE, INTERMEDIATE THEREOF, AND APPLICATION THEREOF SLC7A1, KARS1, LNPEP KMT2A 383/4885MEN1 3020/4885ALDH1A1 1045/4885

“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.