SCHEMBL378767

SCHEMBL378767

O=C(O)Cc1cc(I)c(O)c([N+](=O)[O-])c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
THRA P10827 3/20 0.51
THRB P10828 3/20 0.51
PPARG P37231 3/20 0.51
RXRA P19793 2/20 0.51
ITGB3 P05106 1/20 0.51
ITGAV P06756 1/20 0.51
LMNA P02545 2/20 0.44
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
HTT P42858 1/20 0.44
CYP1A2 P05177 3/20 0.43
CYP2C9 P11712 2/20 0.41
HPGD P15428 2/20 0.41
HIF1A Q16665 2/20 0.41
HSD17B10 Q99714 2/20 0.41
ABCB11 O95342 1/20 0.41
PGR P06401 1/20 0.41
POLB P06746 1/20 0.41
CHRM2 P08172 1/20 0.41
HTR1A P08908 1/20 0.41

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
SCHEMBL30448708 1.00 THRA (0.51) THRATHRBPPARGRXRAITGB3
SCHEMBL4036461 0.88 GPR35 (0.52) MEN1KMT2ACYP1A2CYP2C9HPGD
SCHEMBL5708442 0.86 MEN1 (0.43) THRATHRBPPARGRXRAITGB3
SCHEMBL7673210 0.83 MEN1 (0.39) THRATHRBPPARGRXRAITGB3
SCHEMBL11156541 0.83 TTR (0.53) LMNAMEN1KMT2ACYP1A2CYP2C9
SCHEMBL6647574 0.82 HSP90AB1 (0.49) THRATHRBPPARGRXRAITGB3
SCHEMBL8773706 0.80 THRB (0.71) THRATHRBPPARGRXRAITGB3
SCHEMBL5879457 0.78 ESR1 (0.39) THRATHRBPPARGRXRAITGB3
SCHEMBL11083679 0.77 MEN1 (0.44) LMNAMEN1KMT2AHTTCYP1A2
SCHEMBL1258900 0.77 MEN1 (0.44) LMNAMEN1KMT2AHTTCYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1524988-B1 USE OF A PROTEASOME INHIBITOR IN THE TREATMENT OF FIBROTIC DISEASES CHARITE UNIVERSITAETSMEDIZIN (DE) 2008-04-16 EP claimed
US-20060199772-A1 Use of a proteasome inhibitor in the treatment of endothelial dysfunction and/or in a low-dose proteasome inhibitor therapy CHARITE'-UNIVERSITAETSMEDIZIN BERLIN (DE) 2006-09-07 US claimed
US-20050222043-A1 Use of proteasome inhibitor in the treatment of fibrotic diseases CHARITE-UNIVERSITAETSMEDIZIN BERLIN (DE) 2005-10-06 US claimed
EP-1524977-A2 USE OF A PROTEASOME INHIBITOR IN THE TREATMENT OF ENDOTHELIAL DYSFUNCTION AND/OR IN A LOW-DOSE PROTEASOME INHIBITOR THERAPY Charité - Universitätsmedizin Berlin (DE) 2005-04-27 EP claimed
WO-2004012732-A2 USE OF A PROTEASOME INHIBITOR IN THE TREATMENT OF ENDOTHELIAL DYSFUNCTION AND/OR IN A LOW-DOSE PROTEASOME INHIBITOR THERAPY Charité-Universitätsmedizin Berlin (DE) 2004-02-12 WO claimed
US-12630643-B2 CD40 binding protein, bispecific conjugate thereof and method of treating cancer STRIKE PHARMA AB (SE) 2026-05-19 US disclosed
US-20260083778-A1 GENERATION OF CD4 T CELLS BOSTON MEDICAL CENTER CORPORATION (US) 2026-03-26 US disclosed
EP-4659813-A2 ENGINEERED IMMUNOGLOBULINS WITH ALTERED FCRN BINDING Universitetet I Oslo (NO) 2025-12-10 EP disclosed
EP-3835318-B1 FC-REGION VARIANTS WITH MODIFIED FCRN- AND MAINTAINED PROTEIN A-BINDING PROPERTIES HOFFMANN LA ROCHE (CH) 2025-10-29 EP disclosed
EP-3430039-B1 ENGINEERED IMMUNOGLOBULINS WITH ALTERED FCRN BINDING UNIV OSLO (NO) 2025-10-22 EP disclosed
US-20250263487-A1 METHODS TO MANIPULATE ALPHA-FETOPROTEIN (AFP) THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2025-08-21 US disclosed
US-20250248980-A1 IMMUNE MODULATORY AGENTS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2025-08-07 US disclosed
WO-1992001047-A1 METHODS FOR PRODUCING MEMBERS OF SPECIFIC BINDING PAIRS CAMBRIDGE ANTIBODY TECHNOLOGY LIMITED (GB) 1992-01-23 WO disclosed
WO-1991001368-A1 HAPTEN/ANTI-HAPTEN AFFINITY LINKING IN CELL SEPARATION DYNAL A.S. (NO) 1991-02-07 WO disclosed
WO-1991001335-A1 IgG3 ANTIBODIES WITH SHORTENED HINGE REGION AND A COMPLEMENT ACTIVATION TEST DYNAL A.S. (NO) 1991-02-07 WO disclosed
EP-0396505-A2 Monoclonal antibodies specific for an immunoglobulin isotype CIBA-GEIGY AG (CH) 1990-11-07 EP disclosed
EP-0334300-A1 The use of monoclonal antibodies and conjugates thereof as signals to direct sensitized effector cells to tumor sites NEORX CORPORATION (US) 1989-09-27 EP disclosed
EP-0267779-A2 Human pleiotropic immune factor and muteins thereof Schering Biotech Corporation (US) 1988-05-18 EP disclosed
US-4536479-A DETECTION ON NONIMMUNOGLOBOLIN ANALYTE E. I. DU PONT DE NEMOURS AND COMPANY (US) 1985-08-20 US disclosed
EP-0119629-A2 Use of anti-idiotype antibodies in immunoassay NEW ENGLAND NUCLEAR CORPORATION (US) 1984-09-26 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 (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-20250248980-A1 IMMUNE MODULATORY AGENTS IL2, IL17A, IL2RA THRA 1685/4885THRB 1234/4885PPARG 1491/4885
US-12630643-B2 CD40 binding protein, bispecific conjugate thereof and method of treating cancer CD40, CD40LG, IGSF11 THRA 200/4885THRB 265/4885PPARG 3103/4885
US-20260083778-A1 GENERATION OF CD4 T CELLS CD4, CD2, ICOS THRA 1808/4885THRB 1173/4885PPARG 3082/4885

“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.