SCHEMBL306348

SCHEMBL306348

O=S(=O)(N(c1ccccn1)S(=O)(=O)C(F)(F)F)C(F)(F)F

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
CYP2D6 P10635 1/20 0.37
CYP2C19 P33261 1/20 0.37
POLB P06746 1/20 0.36
TSHR P16473 2/20 0.35
ATM Q13315 1/20 0.35
HSD17B10 Q99714 2/20 0.35
NPSR1 Q6W5P4 2/20 0.35
NFE2L2 Q16236 2/20 0.35
KMT2A Q03164 2/20 0.35
NPC1 O15118 1/20 0.35
RAB9A P51151 1/20 0.35
HTT P42858 1/20 0.35
KDM4E B2RXH2 3/20 0.35
HPGD P15428 1/20 0.35
MAPT P10636 1/20 0.35
POLQ O75417 1/20 0.35
LMNA P02545 1/20 0.34
HDAC1 Q13547 1/20 0.33

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
SCHEMBL29443546 1.00 ALDH1A1 (0.41) ALDH1A1SMN1; SMN2CYP2D6CYP2C19POLB
SCHEMBL17263229 0.87 ALDH1A1 (0.39) ALDH1A1SMN1; SMN2CYP2D6CYP2C19POLB
SCHEMBL15557360 0.84 ALDH1A1 (0.50) ALDH1A1SMN1; SMN2HSD17B10NPSR1KMT2A
SCHEMBL14307527 0.82 ALDH1A1 (0.43) ALDH1A1SMN1; SMN2CYP2D6CYP2C19POLB
SCHEMBL11336157 0.80 POLB (0.38) ALDH1A1SMN1; SMN2POLBTSHRHSD17B10
SCHEMBL5535038 0.79 PGK1 (0.31)
SCHEMBL5539664 0.78 NFE2L2 (0.31) NFE2L2
SCHEMBL254106 0.75 ALDH1A1 (0.57) ALDH1A1SMN1; SMN2CYP2D6CYP2C19POLB
SCHEMBL5706368 0.74 ALDH1A1 (0.41) ALDH1A1SMN1; SMN2CYP2D6CYP2C19TSHR
SCHEMBL29978275 0.74 ALDH1A1 (0.33) ALDH1A1NFE2L2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4658652-A2 PROCESSES AND INTERMEDIATES FOR SYNTHESIS OF ADAGRASIB Mirati Therapeutics, Inc. (US) 2025-12-10 EP claimed
EP-4656639-A1 METHOD FOR THE PREPARATION OF IBOGAMINE AND PURIFICATION OF IBOGAMINE AND IBOGAMINE-TYPE COMPOUNDS Oeri, Hans (CA) 2025-12-03 EP claimed
CN-119481273-A Electrolyte, battery and electric equipment 厦门海辰储能科技股份有限公司 2025-02-18 CN claimed
US-20240368063-A1 PREPARATION METHOD, INTERMEDIATE COMPOUNDS, AND SYNTHESIS METHOD FOR A CLASS OF ANTHRACENE-DERIVED TOXINS IN ORGANIC CHEMISTRY WUYAN PHARMACEUTICAL TECHNOLOGY (SHANGHAI) CO., LTD (CN) 2024-11-07 US claimed
WO-2024163626-A2 PROCESSES AND INTERMEDIATES FOR SYNTHESIS OF ADAGRASIB Mirati Therapeutics, Inc. (US) 2024-08-08 WO claimed
CN-115650827-B Preparation method, intermediate compound and synthesis method for anthracycline derivatives 戊言医药科技(上海)有限公司 2024-03-15 CN claimed
CN-117352668-A Preparation method of pyrophosphate secondary battery positive electrode material with high air stability 深圳珈钠能源科技有限公司 2024-01-05 CN claimed
EP-3694853-B1 PROCESS FOR THE PREPARATION OF 6-(2-HYDROXY-2-METHYLPROPOXY)-4-(6-(6-((6-METHOXYPYRIDIN-3-YL)METHYL)-3,6-DIAZABICYCLO[3.1.1]HEPTAN-3-YL)PYRIDIN-3-YL)PYRAZOLO[1,5-A]PYRIDINE-3-CARBONITRILE ARRAY BIOPHARMA INC (US) 2023-05-17 EP claimed
CN-115650827-A Preparation method, intermediate compound and synthesis method for anthracycline derivatives 戊言医药科技(上海)有限公司 2023-01-31 CN claimed
CN-109575060-B Synthesis of spiro bisboron catalyst and application of spiro bisboron catalyst in hydrogenation reaction 南开大学 2020-11-17 CN claimed
US-8404789-B2 Olefin polymerization catalyst and preparation method and use thereof PETROCHINA COMPANY LIMITED (CN) 2013-03-26 US claimed
US-20110207900-A1 CATALYST FOR HOMOPOLYMERIZING AND COPOLYMERIZING PROPYLENE AND ITS PREPARATION AND USE PETROCHINA COMPANY LIMITED (CN) 2011-08-25 US claimed
EP-2345675-A1 A CATALYST FOR HOMOPOLYMERIZING AND COPOLYMERIZING PROPYLENE AND ITS PREPARATION AND USE Petrochina Company Limited (CN) 2011-07-20 EP claimed
US-20100184930-A1 OLEFIN POLYMERIZATION CATALYST AND PREPARATION METHOD AND USE THEREOF PETROCHINA COMPANY LIMITED (CN) 2010-07-22 US claimed
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 EP claimed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 EP claimed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 US claimed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 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 (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-20240368063-A1 PREPARATION METHOD, INTERMEDIATE COMPOUNDS, AND SYNTHESIS METHOD FOR A CLASS OF ANTHRACENE-DERIVED TOXINS IN ORGANIC CHEMISTRY ANTXR2, AKR7A2, ACR ALDH1A1 1295/4885SMN1; SMN2 3727/4885CYP2D6 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.