SCHEMBL23025

SCHEMBL23025

O=S(=O)(Cl)c1ccccn1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.55
PKM P14618 2/20 0.55
TDP1 Q9NUW8 2/20 0.48
ALDH1A1 P00352 1/20 0.48
HSD17B10 Q99714 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.47
NFE2L2 Q16236 4/20 0.43
SLC40A1 Q9NP59 2/20 0.42
MAOA P21397 1/20 0.42
MAOB P27338 1/20 0.42
LOX P28300 1/20 0.42
GLO1 Q04760 1/20 0.42
TXNRD1 Q16881 1/20 0.41
POLB P06746 2/20 0.40
LMNA P02545 2/20 0.40
CYP1A2 P05177 1/20 0.40
CCR1 P32246 1/20 0.40
CCR5 P51681 1/20 0.40
CCR8 P51685 1/20 0.40
METAP1 P53582 1/20 0.40

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
SCHEMBL29650217 1.00 KDM4E (0.55) KDM4EPKMTDP1ALDH1A1HSD17B10
Hydrochloric Acid SCHEMBL17129 0.98 KDM4E (0.53) KDM4EPKMTDP1ALDH1A1HSD17B10
SCHEMBL1673906 0.80 KDM4E (0.64) KDM4EPKML3MBTL1NFE2L2SLC40A1
SCHEMBL329498 0.78 KDM4E (0.52) KDM4EPKMTDP1L3MBTL1NFE2L2
Valine SCHEMBL724587 0.78 SLC7A5 (0.43) KDM4EPKMTDP1ALDH1A1HSD17B10
SCHEMBL24214242 0.76 KDM4E (0.50) KDM4EPKMTDP1L3MBTL1NFE2L2
SCHEMBL34548 0.76 KDM4E (0.50) KDM4EPKMTDP1ALDH1A1HSD17B10
SCHEMBL18606310 0.76 KDM4E (0.50) KDM4EPKML3MBTL1NFE2L2SLC40A1
SCHEMBL323373 0.76 KDM4E (0.50) KDM4EPKMTDP1ALDH1A1L3MBTL1
SCHEMBL29569774 0.76 KDM4E (0.50) KDM4EPKMTDP1ALDH1A1L3MBTL1

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 1380 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120142523-A Method for detecting isomer impurities in vonolamine fumarate starting material and application of method 北京悦康科创医药科技股份有限公司 2025-06-13 CN claimed
CN-115974903-B Preparation method of 2- (4- (tert-butyl) naphthalene-2-yl) -4, 5-tetramethyl-1, 3, 2-dioxaborane 中钢集团南京新材料研究院有限公司 2024-10-29 CN claimed
CN-118759068-A Method for separating and measuring nitrate radical and nitrite radical residues in pyridine sulfonyl chloride 浙江国邦药业有限公司 2024-10-11 CN claimed
CN-118084792-A Pyrazole-5-sulfonamide derivative, and preparation method and application thereof 安徽农业大学 2024-05-28 CN claimed
CN-117510551-A Pyridine sulfonamide iridium complex, preparation method and high-selectivity catalytic regeneration of NADH (NADH) 烟台大学 2024-02-06 CN claimed
CN-112300123-B Preparation method of voronoi intermediate 上海天慈国际药业有限公司 2023-07-18 CN claimed
CN-115974903-A Preparation method of 2- (4- (tert-butyl) naphthalene-2-yl) -4, 5-tetramethyl-1, 3, 2-dioxaborane 中钢集团南京新材料研究院有限公司 2023-04-18 CN claimed
CN-112939955-B 8- (pyridine amide) substituted coumarin compound and preparation method and application thereof 朗捷睿(苏州)生物科技有限公司 2022-10-21 CN claimed
WO-2022183963-A1 8-(PICOLINAMIDE) SUBSTITUTED COUMARIN COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 朗捷睿(苏州)生物科技有限公司 2022-09-09 WO claimed
CN-114195694-A Preparation method of pyrrole compound 广东东阳光药业有限公司 2022-03-18 CN claimed
US-20030055290-A1 Hydrogen reduction of sulfonyl chlorides to thiols THE TEXAS A&M UNIVERSITY SYSTEM 2003-03-20 US claimed
US-6531605-B1 Reacting diazonium salt of aminopyridine or aminobenzene with thionyl chloride in water, electron transfer catalyst; 2-chloropyridine-3-sulfonyl chloride; avoids use of acetic acid and sulfur dioxide; no extraction isolation problems ZENECA LIMITED (GB) 2003-03-11 US claimed
EP-1265858-A1 HYDROGEN REDUCTION OF SULFONYL CHLORIDES TO THIOLS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2002-12-18 EP claimed
US-6310214-B1 FROM HYDROXYPYRIDINESULPHONIC ACIDS COMPRISING PASSING CHLORINE GAS INTO A MIXTURE OF A HYDROXYPYRIDINESULPHONIC ACID AND OF PHOSPHORUS TRICHLORIDE; HEATING; DISTILLATION RUETGERS ORGANICS GMBH (DE) 2001-10-30 US claimed
WO-2001066517-A1 HYDROGEN REDUCTION OF SULFONYL CHLORIDES TO THIOLS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2001-09-13 WO claimed
EP-1048654-A2 Process for the preparation of chloropyridine sulfonyl chloride Rütgers Organics GmbH (DE) 2000-11-02 EP claimed
WO-2000063177-A1 METHOD OF PRODUCING CHLOROPYRIDINE SULFONIC ACID CHLORIDES RÜTGERS ORGANICS GMBH (DE) 2000-10-26 WO claimed
EP-0973704-A1 PROCESS FOR THE MANUFACTURE OF ARYLSULFONYL CHLORIDE ZENECA LIMITED (GB) 2000-01-26 EP claimed
WO-1998040332-A1 PROCESS FOR THE MANUFACTURE OF ARYLSULFONYL CHLORIDE ZENECA LIMITED (GB) 1998-09-17 WO claimed
EP-0581738-A1 Herbizidal pyridylsulfonyl ureas CIBA-GEIGY AG (CH) 1994-02-02 EP 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 (1 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-20030055290-A1 Hydrogen reduction of sulfonyl chlorides to thiols TST, IAPP, CBS KDM4E 1181/4885PKM 44/4885TDP1 2896/4885

“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.