SCHEMBL565121

SCHEMBL565121

O=S(=O)(SS(=O)(=O)c1ccccc1)c1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 2/20 0.55
ALDH1A1 P00352 3/20 0.50
CA1 P00915 2/20 0.50
CA2 P00918 2/20 0.50
HSD17B10 Q99714 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
CA12 O43570 1/20 0.50
CA3 P07451 1/20 0.50
CA4 P22748 1/20 0.50
CA6 P23280 1/20 0.50
CA5A P35218 1/20 0.50
CA7 P43166 1/20 0.50
PLA2G7 Q13093 1/20 0.50
CA9 Q16790 1/20 0.50
CA13 Q8N1Q1 1/20 0.50
CA14 Q9ULX7 1/20 0.50
CA5B Q9Y2D0 1/20 0.50
TSHR P16473 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
DUSP3 P51452 1/20 0.48

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
SCHEMBL11323690 0.82 HTR6 (0.55) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL15434593 0.78 HTR6 (0.50) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL28841908 0.78 ALDH1A1 (0.52) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL5166440 0.78 HTR6 (0.50) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL11335316 0.78 HTR6 (0.50) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL135257 0.76 DNMT1 (0.56) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL7618702 0.76 DUSP3 (0.48) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL11568829 0.72 APOBEC3G (0.52) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL10583865 0.72 HPGD (0.48) HTR6ALDH1A1CA1CA2HSD17B10
SCHEMBL11291589 0.72 PSIP1 (0.54) HTR6ALDH1A1CA1CA2HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
CN-118490889-A ROS (reactive oxygen species) responsive hydrogel as well as preparation method and application thereof 华南理工大学 2024-08-16 CN 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-108863871-B Pyrene derivative electroluminescent material and preparation method and application thereof 华南协同创新研究院 2020-12-01 CN claimed
CN-103113387-B The synthetic method of asymmetric two thieno-heteroaromatic compounds HENAN UNIVERSITY (CN) 2016-02-17 CN claimed
EP-1308540-B1 Plating bath and method for depositing a metal layer on a substrate SHIPLEY CO LLC (US) 2010-01-20 EP claimed
US-20040104124-A1 Plating bath and method for depositing a metal layer on a substrate SHIPLEY COMPANY, L.L.C. 2004-06-03 US claimed
US-6736954-B2 A METAL PLATING BATH COMPRISING METAL SALTS AND AN ADDITIVE CONSUMPTION INHIBITOR(A HETEROATOM ORGANIC COMPOUNDS WHICH MAY CONTAIN SULFUR, OXYGEN OR NITROGEN HETEROATOMS) IMPROVE THE BRIGHTNESS OF PLATED METAL AS WELL AS THE DUCTILITY SHIPLEY COMPANY, L.L.C. 2004-05-18 US claimed
EP-1308540-A1 Plating bath and method for depositing a metal layer on a substrate Shipley Co. L.L.C. (US) 2003-05-07 EP claimed
US-20030070934-A1 Plating bath and method for depositing a metal layer on a substrate SHIPLEY COMPANY, L.L.C. 2003-04-17 US claimed
WO-2025235763-A1 FLUORESCENT PROBES AND USES THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2025-11-13 WO disclosed
US-20250122226-A1 GLUCOSE-SENSITIVE ALBUMIN-BINDING DERIVATIVES NOVO NORDISK AS (DK) 2025-04-17 US disclosed
US-12227528-B2 Glucose-sensitive albumin-binding derivatives NOVO NORDISK A/S (DK) 2025-02-18 US disclosed
CN-118490889-A ROS (reactive oxygen species) responsive hydrogel as well as preparation method and application thereof 华南理工大学 2024-08-16 CN disclosed
CN-117624207-A Glucose-sensitive albumin binding derivatives 诺和诺德股份有限公司 2024-03-01 CN disclosed
WO-1997030069-A1 17-BETA-CYCLOPROPYL(AMINO/OXY) 4-AZA STEROIDS AS ACTIVE INHIBITORS OF TESTOSTERONE 5-ALPHA-REDUCTASE AND C17-20-LYASE HOECHST MARION ROUSSEL, INC. (US) 1997-08-21 WO disclosed
EP-0680466-A1 PROCESS FOR PREPARING ISOCYANATES. MONSANTO CO (US) 1995-11-08 EP disclosed
CN-1099384-A Process for preparing isocyanates MONSANTO CO (US) 1995-03-01 CN disclosed
US-5349081-A Dehydration, primary amine and carbon dioxide MONSANTO COMPANY (US) 1994-09-20 US disclosed
WO-1994017032-A1 PROCESS FOR PREPARING ISOCYANATES MONSANTO COMPANY (US) 1994-08-04 WO 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 (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-12227528-B2 Glucose-sensitive albumin-binding derivatives ALB, DBI, FABP4 HTR6 4018/4885ALDH1A1 1240/4885CA1 1665/4885
US-20240368063-A1 PREPARATION METHOD, INTERMEDIATE COMPOUNDS, AND SYNTHESIS METHOD FOR A CLASS OF ANTHRACENE-DERIVED TOXINS IN ORGANIC CHEMISTRY ANTXR2, AKR7A2, ACR HTR6 3877/4885ALDH1A1 1295/4885CA1 277/4885
US-20250122226-A1 GLUCOSE-SENSITIVE ALBUMIN-BINDING DERIVATIVES ALB, DBI, FABP4 HTR6 4018/4885ALDH1A1 1240/4885CA1 1665/4885

“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.