SCHEMBL441353

SCHEMBL441353

O=C1c2ccccc2C(=O)N1S

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ POLB P06746 4/20 0.48
▸ CDC25B P30305 2/20 0.48
▸ EHMT2 Q96KQ7 2/20 0.48
▸ EHMT1 Q9H9B1 2/20 0.48
▸ MAOA P21397 2/20 0.48
▸ IDO1 P14902 2/20 0.48
▸ MAOB P27338 1/20 0.48
▸ AKT1 P31749 1/20 0.48
▸ SNCA P37840 1/20 0.48
▸ MAP2K1 Q02750 1/20 0.48
▸ PIN1 Q13526 1/20 0.48
▸ NSD1 Q96L73 1/20 0.48
▸ CASP3 P42574 1/20 0.46
▸ KMT2A Q03164 6/20 0.45
▸ MEN1 O00255 4/20 0.45
▸ CYP1A2 P05177 1/20 0.44
▸ KDM4E B2RXH2 2/20 0.43
▸ LMNA P02545 2/20 0.43
▸ BCHE P06276 2/20 0.43
▸ PTPRC P08575 2/20 0.43

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
SCHEMBL30728578 1.00 POLB (0.48) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL11119821 0.97 POLB (0.46) POLBCDC25BEHMT2EHMT1MAOA
Propionitrile SCHEMBL8597970 0.81 DRD3 (0.46) CASP3KMT2AMEN1CA12CA9
SCHEMBL454827 0.75 POLB (0.67) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL134793 0.73 POLB (0.56) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL2022462 0.73 POLB (0.64) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL487827 0.71 POLB (0.48) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL14410649 0.71 POLB (0.48) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL1771 0.71 POLB (0.48) POLBCDC25BEHMT2EHMT1MAOA
SCHEMBL7563174 0.71 POLB (0.48) POLBCDC25BEHMT2EHMT1MAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117551023-A Preparation method and application of N-thio-phenyl phthalimide compound 太原理工大学 2024-02-13 — — CN claimed
CN-117447370-A Preparation method of aggregation-induced emission material tetraaryl divinyl sulfide 山西蓬勃健康科技有限公司 2024-01-26 — — CN claimed
CN-113264859-B Naphthalene sulfonamide isothiocyanate bifunctional micromolecules as well as preparation method and application thereof 宁夏医科大学 2023-02-07 — — CN claimed
CN-113264859-A Naphthalene sulfonamide isothiocyanate bifunctional micromolecules as well as preparation method and application thereof 宁夏医科大学 2021-08-17 — — CN claimed
JP-2007505922-A — — 2007-03-15 — — JP claimed
US-20060211728-A1 Thalidomide analogs P2D INC. 2006-09-21 — — US claimed
EP-1663223-A2 THALIDOMIDE ANALOGS AS TNF-ALPHA MODULATORS THE GOVERNMENT OF THE UNITED STATES OF AMERICA, represented by THE DEPARTMENT OF HEALTH & HUMAN SERVICES (US) 2006-06-07 — — EP claimed
WO-2005028436-A2 THALIDOMIDE ANALOGS AS TNF-ALPHA MODULATORS THE GOVERNMENT OF THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2005-03-31 — — WO claimed
US-4808696-A FROM DIANHYDRIDE AND/OR DIIMIDES AND ALKALI METAL SULFIDE GENERAL ELECTRIC COMPANY (US) 1989-02-28 — — US claimed
EP-0293693-A2 Method for making organobis(Thioether)s, and products obtained therefrom GENERAL ELECTRIC COMPANY (US) 1988-12-07 — — EP claimed
WO-2024094566-A1 INDACENE AND AZAINDACENE COMPOUNDS AND HIGHER HOMOLOGUES AND THE USE THEREOF Credoxys GmbH (DE) 2024-05-10 — — WO disclosed
CN-117551023-A Preparation method and application of N-thio-phenyl phthalimide compound 太原理工大学 2024-02-13 — — CN disclosed
CN-117551023-A Preparation method and application of N-thio-phenyl phthalimide compound 太原理工大学 2024-02-13 — — CN disclosed
CN-117447370-A Preparation method of aggregation-induced emission material tetraaryl divinyl sulfide 山西蓬勃健康科技有限公司 2024-01-26 — — CN disclosed
CN-113754621-B Synthesis method of 2,3',3,4' -diphenyl sulfone tetracarboxylic dianhydride 常州市阳光药业有限公司 2023-06-23 — — CN disclosed
EP-0293693-A2 Method for making organobis(Thioether)s, and products obtained therefrom GENERAL ELECTRIC COMPANY (US) 1988-12-07 — — EP disclosed
US-4729986-A AGRICULTURE E. I. DU PONT DE NEMOURS AND COMPANY (US) 1988-03-08 — — US disclosed
EP-0251086-A2 Antifungal carbinols THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1988-01-07 — — EP disclosed
US-4409018-A HERBICIDES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1983-10-11 — — US disclosed
EP-0041256-A1 Hexahydroisoindol derivatives, process for producing said compounds and herbicides containing said compounds Takeda Chemical Industries, Ltd. (JP) 1981-12-09 — — EP 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 (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-20060211728-A1 Thalidomide analogs TNF, TNFRSF1A, PGF POLB 2461/4885CDC25B 200/4885EHMT2 4195/4885

“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.

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