SCHEMBL1933183

SCHEMBL1933183

Cc1ccc(S(=O)(=O)/N=C/c2ccccc2)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.67
POLB P06746 3/20 0.67
KMT2A Q03164 5/20 0.59
LMNA P02545 4/20 0.54
GAA P10253 1/20 0.54
MEN1 O00255 4/20 0.50
KDM4E B2RXH2 3/20 0.48
HTT P42858 2/20 0.48
CRHBP P24387 1/20 0.48
CRHR2 Q13324 1/20 0.48
MAPT P10636 2/20 0.46
TDP1 Q9NUW8 1/20 0.46
NPSR1 Q6W5P4 1/20 0.46
ATM Q13315 1/20 0.46
PTGS2 P35354 2/20 0.45
PTGS1 P23219 1/20 0.45
CA12 O43570 1/20 0.45
CA2 P00918 1/20 0.45
CA9 Q16790 1/20 0.45
F2 P00734 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
SCHEMBL1933186 1.00 ALDH1A1 (0.67) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL3104931 1.00 ALDH1A1 (0.67) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL1933496 0.93 ALDH1A1 (0.69) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL1933497 0.93 ALDH1A1 (0.69) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL307938 0.91 ALDH1A1 (0.78) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL16802983 0.91 ALDH1A1 (0.78) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL10073012 0.91 ALDH1A1 (0.78) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL1933484 0.87 ALDH1A1 (0.69) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL12699925 0.87 ALDH1A1 (0.69) ALDH1A1POLBKMT2ALMNAGAA
SCHEMBL984789 0.87 ALDH1A1 (0.69) ALDH1A1POLBKMT2ALMNAGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114380695-A Novel method for simply and quickly realizing C-C bond forming reaction 吉林大学 2022-04-22 CN claimed
CN-107235886-B Synthesis method of 2, 3-dihydropyrrole ring 合肥工业大学 2020-04-07 CN claimed
US-8323356-B2 Sulfonimines as bleaching activators HENKEL AG & CO. KGAA (DE) 2012-12-04 US claimed
EP-2503984-A1 SULFONIMINES AS BLEACHING ACTIVATORS Henkel AG & Co. KGaA (DE) 2012-10-03 EP claimed
US-20120227756-A1 SULFONIMINES AS BLEACHING ACTIVATORS HENKEL AG & CO. KGAA (DE) 2012-09-13 US claimed
WO-2011064007-A1 SULFONIMINES AS BLEACHING ACTIVATORS HENKEL AG & CO. KGAA (DE) 2011-06-03 WO claimed
US-12378193-B2 Anti-arrhythmicity agents THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2025-08-05 US disclosed
CN-118978480-A Through C (sp)3) Green synthesis method for synthesizing quinoline derivative by synthesizing H bond functional group 东南大学成贤学院 2024-11-19 CN disclosed
CN-117645551-A Imine compound and preparation method thereof 苏州新启材料科技有限公司 2024-03-05 CN disclosed
CN-114380695-B Novel method for simply and rapidly realizing C-C bond formation reaction 吉林大学 2024-02-13 CN disclosed
CN-114380695-B Novel method for simply and rapidly realizing C-C bond formation reaction 吉林大学 2024-02-13 CN disclosed
US-20230150935-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR MODULATING CALCIUM ION HOMEOSTASIS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2023-05-18 US disclosed
US-20230150935-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR MODULATING CALCIUM ION HOMEOSTASIS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2023-05-18 US disclosed
US-20110178138-A1 INHIBITORS OF PROTEIN PRENYLTRANSFERASES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2011-07-21 US disclosed
WO-2011064007-A1 SULFONIMINES AS BLEACHING ACTIVATORS HENKEL AG & CO. KGAA (DE) 2011-06-03 WO disclosed
US-20110071310-A1 DIAMINO ACID DERIVATIVE STARTING MATERIAL, MANUFACTURING METHOD THEREOF, AND DIAMINO ACID DERIVATIVE MANUFACTURING METHOD JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2011-03-24 US disclosed
US-20110071310-A1 DIAMINO ACID DERIVATIVE STARTING MATERIAL, MANUFACTURING METHOD THEREOF, AND DIAMINO ACID DERIVATIVE MANUFACTURING METHOD JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2011-03-24 US disclosed
EP-2269979-A1 DIAMINO ACID DERIVATIVE STARTING MATERIAL, MANUFACTURING METHOD THEREOF, AND DIAMINO ACID DERIVATIVE MANUFACTURING METHOD Japan Science and Technology Agency (JP) 2011-01-05 EP disclosed
US-20100234395-A1 UREIDE DERIVATIVE AND PHARMACEUTICAL APPLICATION THEREOF TORAY INDUSTRIES, INC. (JP) 2010-09-16 US disclosed
US-20100234395-A1 UREIDE DERIVATIVE AND PHARMACEUTICAL APPLICATION THEREOF TORAY INDUSTRIES, INC. (JP) 2010-09-16 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 (6 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-20230150935-A1 COMPOUNDS, COMPOSITIONS, AND METHODS FOR MODULATING CALCIUM ION HOMEOSTASIS CHERP, ATP2A1, ATP2A3 ALDH1A1 3911/4885POLB 4857/4885KMT2A 4698/4885
US-20110071310-A1 DIAMINO ACID DERIVATIVE STARTING MATERIAL, MANUFACTURING METHOD THEREOF, AND DIAMINO ACID DERIVATIVE MANUFACTURING METHOD DAO, DDC, DCTD ALDH1A1 131/4885POLB 378/4885KMT2A 280/4885
US-20120227756-A1 SULFONIMINES AS BLEACHING ACTIVATORS KRT18, SQOR, GPX4 ALDH1A1 232/4885POLB 348/4885KMT2A 430/4885
US-20110178138-A1 INHIBITORS OF PROTEIN PRENYLTRANSFERASES RABGGTA, FNTA, RABGGTB ALDH1A1 2160/4885POLB 3212/4885KMT2A 2553/4885
US-12378193-B2 Anti-arrhythmicity agents KCNH1, TNNI3, TNNC1 ALDH1A1 806/4885POLB 1643/4885KMT2A 4017/4885
US-20100234395-A1 UREIDE DERIVATIVE AND PHARMACEUTICAL APPLICATION THEREOF UROD, UTS2R, SLC14A1 ALDH1A1 1908/4885POLB 4859/4885KMT2A 3421/4885

“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.