SCHEMBL133934

SCHEMBL133934

O=C1NC(=O)c2c(CCCCCCBr)cccc21

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 2/20 0.38
KDM4E B2RXH2 4/20 0.38
ALDH1A1 P00352 4/20 0.38
GAA P10253 1/20 0.38
HPGD P15428 1/20 0.38
HSD17B10 Q99714 1/20 0.38
PARP1 P09874 4/20 0.37
CASP3 P42574 5/20 0.34
CASP7 P55210 2/20 0.34
CASP2 P42575 1/20 0.34
CASP6 P55212 1/20 0.34
CASP8 Q14790 1/20 0.34
GSK3A P49840 1/20 0.34
CDK5 Q00535 1/20 0.34
CDK5R1 Q15078 1/20 0.34
NPSR1 Q6W5P4 2/20 0.33
PDGFRA P16234 1/20 0.33
FER P16591 1/20 0.33
LTK P29376 1/20 0.33
CDK8 P49336 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
SCHEMBL9152783 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL4206081 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL4909203 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL4026807 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL8938070 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL31036258 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL9151570 1.00 GSK3B (0.38) GSK3BKDM4EALDH1A1GAAHPGD
SCHEMBL1234203 0.98 GSK3B (0.39) GSK3BKDM4EALDH1A1GAAHPGD
Phthalimide SCHEMBL8559536 0.97 GSK3B (0.44) GSK3BKDM4EALDH1A1GAAHPGD
Phthalimide SCHEMBL8558696 0.96 GSK3B (0.43) GSK3BKDM4EALDH1A1GAAHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114773222-A Synthetic method of azo micromolecules for zinc oxide nanoparticle stable ligand 宁波大学 2022-07-22 CN claimed
EP-4700124-A2 OLIGONUCLEOTIDE-LIGAND CONJUGATES AND PROCESS FOR THEIR PREPARATION Alnylam Pharmaceuticals, Inc. (US) 2026-02-25 EP disclosed
US-20250075208-A1 OLIGONUCLEOTIDE-LIGAND CONJUGATES AND PROCESS FOR THEIR PREPARATION BANK OF AMERICA, N.A. 2025-03-06 US disclosed
EP-4496590-A1 PROTEOLYSIS TARGETING CHIMERA (PROTAC) MOLECULE FOR DEGRADATION OF ENL AND CANCER THERAPY Baylor College of Medicine (US) 2025-01-29 EP disclosed
US-12173288-B2 Oligonucleotide-ligand conjugates and process for their preparation ALNYLAM PHARMACEUTICALS, INC. (US) 2024-12-24 US disclosed
CN-114773222-B Synthesis method of azo micromolecules for zinc oxide nanoparticle stable ligand 宁波大学 2024-04-09 CN disclosed
WO-2023183412-A1 PROTEOLYSIS TARGETING CHIMERA (PROTAC) MOLECULE FOR DEGRADATION OF ENL AND CANCER THERAPY BAYLOR COLLEGE OF MEDICINE (US) 2023-09-28 WO disclosed
US-20220348914-A1 OLIGONUCLEOTIDE-LIGAND CONJUGATES AND PROCESS FOR THEIR PREPARATION BANK OF AMERICA, N.A. 2022-11-03 US disclosed
EP-4039278-A1 OLIGONUCLEOTIDE-LIGAND CONJUGATES AND PROCESS FOR THEIR PREPARATION Alnylam Pharmaceuticals, Inc. (US) 2022-08-10 EP disclosed
CN-114773222-A Synthetic method of azo micromolecules for zinc oxide nanoparticle stable ligand 宁波大学 2022-07-22 CN disclosed
EP-0728139-A1 AMINE-DERIVATIZED NUCLEOSIDES AND OLIGONUCLEOSIDES ISIS PHARMACEUTICALS, INC. (US) 1996-08-28 EP disclosed
US-5543507-A BONDING STRANDS OR ONE STRAND AT DIFFERENT SITES; RNA MIMICS FIXED IN SPATIAL CONFORMATION; NUCLEASE RESISTANT MIMICS OF BINDING RECEPTORS FOR NUCLEIC ACID-BINDING PROTEINS; 5-LIPOXYGENASE INHIBITORS; DIAGNOSIS; ANALYZING ISIS PHARMACEUTICALS, INC. (US) 1996-08-06 US disclosed
EP-0635023-A4 COVALENTLY CROSS-LINKED OLIGONUCLEOTIDES. ISIS PHARMACEUTICALS INC (US) 1996-03-20 EP disclosed
US-5424451-A Used as cholinesterase activity inhibitors MEDIOLANUM FARMACEUTICI S.P.A. (IT) 1995-06-13 US disclosed
WO-1995006659-A1 AMINE-DERIVATIZED NUCLEOSIDES AND OLIGONUCLEOSIDES ISIS PHARMACEUTICALS, INC. (US) 1995-03-09 WO disclosed
EP-0635023-A1 COVALENTLY CROSS-LINKED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 1995-01-25 EP disclosed
US-5302593-A Aminoalkylcarbamic esters of eseroline suitable for use as chlorinesterase activity inhibitors MEDIOLANUM FARMACEUTICI S.P.A. (IT) 1994-04-12 US disclosed
EP-0575954-A1 Aminoalkylcarbamic esters of eseroline suitable for use as cholinesterase acitivity inhibitors and relative preparation process MEDIOLANUM FARMACEUTICI S.P.A. (IT) 1993-12-29 EP disclosed
WO-1993018052-A1 COVALENTLY CROSS-LINKED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 1993-09-16 WO disclosed
US-4705892-A Process for preparing alpha,omega-diamino acids MERCK & CO., INC. (US) 1987-11-10 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 (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-20220348914-A1 OLIGONUCLEOTIDE-LIGAND CONJUGATES AND PROCESS FOR THEIR PREPARATION IGF2R, IRS1, INSR GSK3B 4633/4885KDM4E 4685/4885ALDH1A1 1084/4885
US-12173288-B2 Oligonucleotide-ligand conjugates and process for their preparation IGF2R, IRS1, INSR GSK3B 4633/4885KDM4E 4685/4885ALDH1A1 1084/4885
US-20250075208-A1 OLIGONUCLEOTIDE-LIGAND CONJUGATES AND PROCESS FOR THEIR PREPARATION IGF2R, IRS1, INSR GSK3B 4633/4885KDM4E 4685/4885ALDH1A1 1084/4885

“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.