SCHEMBL25105

SCHEMBL25105

O=[N+]([O-])c1ccccc1I

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.54
TDP1 Q9NUW8 5/20 0.52
ALDH1A1 P00352 8/20 0.50
KMT2A Q03164 2/20 0.50
MEN1 O00255 1/20 0.50
GPR35 Q9HC97 1/20 0.50
TSHR P16473 2/20 0.48
NPC1 O15118 1/20 0.47
RECQL P46063 1/20 0.47
RAB9A P51151 1/20 0.47
PARP1 P09874 1/20 0.46
MAPK1 P28482 1/20 0.45
CASP7 P55210 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
LMNA P02545 1/20 0.44
HPGD P15428 1/20 0.44
PLAU P00749 1/20 0.44
PTPRC P08575 1/20 0.44
S100A4 P26447 1/20 0.44

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
SCHEMBL10379786 1.00 HSD17B10 (0.54) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL28554564 1.00 HSD17B10 (0.54) HSD17B10TDP1ALDH1A1KMT2AMEN1
Formic Acid SCHEMBL28004034 0.89 GPR35 (0.47) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL28155215 0.88 HPGD (0.51) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL10379315 0.84 HSD17B10 (0.41) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL9641571 0.84 HSD17B10 (0.41) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL9641590 0.82 PTPRC (0.40) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL7531431 0.81 TDP1 (0.54) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL22566 0.81 HSD17B10 (0.67) HSD17B10TDP1ALDH1A1KMT2AMEN1
SCHEMBL29577518 0.81 HSD17B10 (0.67) HSD17B10TDP1ALDH1A1KMT2AMEN1

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 1799 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119752437-A Organic electroluminescent material containing double main bodies, preparation method and application thereof 吉林奥来德光电材料股份有限公司 2025-04-04 CN claimed
CN-119069693-A Negative electrode slurry, negative electrode plate, battery monomer, battery and electric equipment 宁德时代新能源科技股份有限公司 2024-12-03 CN claimed
CN-118874537-A Catalyst, preparation method thereof and method for preparing aromatic amine compound 厦门大学 2024-11-01 CN claimed
US-20240294482-A1 METHOD FOR CATALYTICALLY ACTIVATING CARBON DIOXIDE AS CARBONYLATION REAGENT WITH INORGANIC SULFUR INNER MONGOLIA UNIVERSITY OF TECHNOLOGY (CN) 2024-09-05 US claimed
CN-118320835-A Catalyst, preparation method thereof and method for preparing arylamine compound 厦门大学 2024-07-12 CN claimed
CN-118179542-A Carbon-based catalyst, and preparation method and application thereof 中国石油化工股份有限公司 2024-06-14 CN claimed
WO-2024013308-A2 METHOD OF REDUCING NITRO COMPOUNDS THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW (GB) 2024-01-18 WO claimed
CN-117208932-A Denitrification method, environment-friendly waste treatment method and preparation method of compound 西南大学 2023-12-12 CN claimed
CN-117209411-A Synthesis method of indolal and derivative thereof 苏州翔实医药发展有限公司 2023-12-12 CN claimed
CN-116745273-A Method for catalyzing and activating carbon dioxide by using inorganic sulfur as carbonylation reagent 内蒙古工业大学 2023-09-12 CN claimed
WO-2002090522-A2 USE OF PHOSPHOROTHIOLATE POLYNUCLEOTIDES IN LIGATING NUCLEIC ACIDS SAN DIEGO STATE UNIVERSITY FOUNDATION (US) 2002-11-14 WO claimed
US-20020015826-A1 Zwitterionic iodonium compounds and methods of application CLEMSON UNIVERSITY 2002-02-07 US claimed
US-5552410-A 1,2,3,4,-tetrahydroquinoline-8-sulphonic acid chlorides and acids, their preparation and their use as synthetic intermediates SYNTHELABO (FR) 1996-09-03 US claimed
EP-0643046-A1 1,2,3,4-Tetrahydrochinolin-8-sulfonic acid and its chlorides as intermediates SYNTHELABO (FR) 1995-03-15 EP claimed
US-5094545-A Solid solution with nucleating agent and indicator dye PYMA CORPORATION (US) 1992-03-10 US claimed
EP-0225478-B1 IODONIUM YLIDE ANTIMICROBIAL COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1990-05-16 EP claimed
EP-0070198-B1 RADIATION-SENSITIVE COMPOSITION AND PATTERN-FORMATION METHOD USING THE SAME Hitachi, Ltd. (JP) 1985-06-19 EP claimed
EP-0070198-A1 Radiation-sensitive composition and pattern-formation method using the same Hitachi, Ltd. (JP) 1983-01-19 EP claimed
US-4232552-A THERMOCHROMISM, DISPOSABLE THERMOMETERS AKZONA INCORPORATED (US) 1980-11-11 US claimed
US-4007221-A Manufacture of nuclear-iodinated iodine compounds of aromatic character BASF AKTIENGESELLSCHAFT (DT) 1977-02-08 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 (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-20240294482-A1 METHOD FOR CATALYTICALLY ACTIVATING CARBON DIOXIDE AS CARBONYLATION REAGENT WITH INORGANIC SULFUR TST, CBR3, SMOX HSD17B10 1617/4885TDP1 4411/4885ALDH1A1 639/4885
US-20020015826-A1 Zwitterionic iodonium compounds and methods of application DGKI, DSTN, PCNA HSD17B10 3530/4885TDP1 4134/4885ALDH1A1 3578/4885

“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.