Bortezomib

Bortezomib

SCHEMBL466239

CC(C)CC(NC(=O)C(Cc1ccccc1)NC(=O)c1cnccn1)B(O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRM1PSMA1PSMA2PSMA3PSMA4PSMA5PSMA6PSMA7PSMA8PSMB1PSMB10PSMB11PSMB2PSMB3PSMB4PSMB5PSMB6PSMB7PSMB8PSMB9PSMC1PSMC2PSMC3PSMC4PSMC5PSMC6PSMD1PSMD11PSMD12PSMD13PSMD14PSMD2PSMD3PSMD4PSMD6PSMD7PSMD8SEM1

The experimentally established mechanism targets of Bortezomib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PSMB5 known ✓ P28074 16/20 1.00
PSMB8 known ✓ P28062 8/20 1.00
PSMB9 known ✓ P28065 8/20 1.00
PSMB6 known ✓ P28072 8/20 1.00
PSMB10 known ✓ P40306 8/20 1.00
PSMB11 known ✓ A5LHX3 7/20 1.00
PSMA7 known ✓ O14818 7/20 1.00
PSMB1 known ✓ P20618 7/20 1.00
PSMA1 known ✓ P25786 7/20 1.00
PSMA2 known ✓ P25787 7/20 1.00
PSMA3 known ✓ P25788 7/20 1.00
PSMA4 known ✓ P25789 7/20 1.00
PSMA5 known ✓ P28066 7/20 1.00
PSMB4 known ✓ P28070 7/20 1.00
PSMB3 known ✓ P49720 7/20 1.00
PSMB2 known ✓ P49721 7/20 1.00
PSMA6 known ✓ P60900 7/20 1.00
PSMA8 known ✓ Q8TAA3 7/20 1.00
PSMB7 known ✓ Q99436 7/20 1.00
PSMD11 known ✓ O00231 1/20 1.00

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
Bortezomib SCHEMBL8036967 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL29377226 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL685473 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL192129 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL30316729 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL8035134 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL8049740 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL8099424 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL3676 1.00 PSMB5 (1.00) PSMB5LONP1PSMB8PSMB9PSMB6
Bortezomib SCHEMBL17075366 0.99 PSMB5 (0.98) PSMB5LONP1PSMB8PSMB9PSMB6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240148728-A1 NOVEL METHOD TO BLOCK INFLAMMATORY CELL DEATH AND IL-1BETA SECRETION CAUSED BY RIBOTOXINS AND UV IRRADIATION USING GENETIC AND CHEMICAL INHIBITORS OF ZAKA AND THE NLRP1 INFLAMMASOME AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2024-05-09 US claimed
EP-4297788-A1 NOVEL METHOD TO BLOCK INFLAMMATORY CELL DEATH AND IL-1BETA SECRETION CAUSED BY RIBOTOXINS AND UV IRRADIATION USING GENETIC AND CHEMICAL INHIBITORS OF ZAKA AND THE NLRP1 INFLAMMASOME Nanyang Technological University (SG) 2024-01-03 EP claimed
US-20230172933-A1 USE OF A COMPOUND OR COMPOSITION COMPRISING AN INHIBITOR OF NLRP1 INFLAMMASOME ACTIVATION FOR THE TREATMENT OF HUMAN AIRWAY INFLAMMATION NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2023-06-08 US claimed
WO-2022182292-A1 NOVEL METHOD TO BLOCK INFLAMMATORY CELL DEATH AND IL-1BETA SECRETION CAUSED BY RIBOTOXINS AND UV IRRADIATION USING GENETIC AND CHEMICAL INHIBITORS OF ZAKA AND THE NLRP1 INFLAMMASOME NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2022-09-01 WO claimed
WO-2021188052-A1 USE OF A COMPOUND OR COMPOSITION COMPRISING AN INHIBITOR OF NLRP1 INFLAMMASOME ACTIVATION FOR THE TREATMENT OF HUMAN AIRWAY INFLAMMATION NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2021-09-23 WO claimed
EP-3110828-B1 CONTINUOUS FLOW PEPTIDE SYNTHESIS UNIV SZEGEDI (HU) 2020-12-09 EP claimed
US-20180243217-A1 NANOPARTICLES COMPRISING A STABILIZED BORONIC ACID COMPOUND LEON-NANODRUGS GMBH (DE) 2018-08-30 US claimed
US-20170360872-A1 USE OF UBIQUITIN-PROTEASOME SYSTEM INHIBITORS FOR TREATMENT OF TUMORS ASSOCIATED WITH NEUROFIBROMATOSIS TYPE-2 BIOXCEL CORPORATION (US) 2017-12-21 US claimed
US-20250043014-A1 ANTIBODY MOLECULES TO APRIL AND USES THEREOF Visterra, Inc. (US) 2025-02-06 US disclosed
EP-4368185-A1 COMBINATION OF MENIN INHIBITOR(S) AND IMMUNOPROTEASE INHIBITOR(S) FOR TREATMENT OF LEUKEMIA Universitätsmedizin Greifswald (DE) 2024-05-15 EP disclosed
US-20240148728-A1 NOVEL METHOD TO BLOCK INFLAMMATORY CELL DEATH AND IL-1BETA SECRETION CAUSED BY RIBOTOXINS AND UV IRRADIATION USING GENETIC AND CHEMICAL INHIBITORS OF ZAKA AND THE NLRP1 INFLAMMASOME AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2024-05-09 US disclosed
CN-117820347-A Method for synthesizing bortezomib by continuous flow 深圳智微通科技有限公司 2024-04-05 CN disclosed
EP-4297788-A1 NOVEL METHOD TO BLOCK INFLAMMATORY CELL DEATH AND IL-1BETA SECRETION CAUSED BY RIBOTOXINS AND UV IRRADIATION USING GENETIC AND CHEMICAL INHIBITORS OF ZAKA AND THE NLRP1 INFLAMMASOME Nanyang Technological University (SG) 2024-01-03 EP disclosed
CN-110799193-B Copper and nickel catalyzed decarboxylation borylation 斯克利普斯研究院 2023-12-12 CN disclosed
WO-2011029802-A1 4-SUBSTITUTED PYRIDIN-3-YL-CARBOXAMIDE COMPOUNDS AND METHODS OF USE F. HOFFMANN-LA ROCHE AG (CH) 2011-03-17 WO disclosed
US-20110059961-A1 4-SUBSTITUTED PYRIDIN-3-YL-CARBOXAMIDE COMPOUNDS AND METHODS OF USE GENENTECH, INC. 2011-03-10 US disclosed
WO-2010105008-A2 COMBINATIONS OF PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND CHEMOTHERAPEUTIC AGENTS FOR THE TREATMENT OF HEMATOPOIETIC MALIGNANCIES GENENTECH, INC. (US) 2010-09-16 WO disclosed
US-20090131367-A1 Combinations of HDAC Inhibitors and Proteasome Inhibitors THE REGENTS OF THE UNIVERSITY OF COLORADO (US) 2009-05-21 US disclosed
WO-2009036281-A2 BORTEZOMIB AND PROCESS FOR PRODUCING SAME DR. REDDY'S LABORATORIES LTD. (IN) 2009-03-19 WO disclosed
WO-2003077928-A1 PEPTIDE ANALOGUES AND USES THEREOF ARIAD PHARMACEUTICALS, INC. (US) 2003-09-25 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-20090131367-A1 Combinations of HDAC Inhibitors and Proteasome Inhibitors HDAC6, HDAC5, HDAC1 PSMB5 25/4885PSMB8 39/4885PSMB9 52/4885
US-20180243217-A1 NANOPARTICLES COMPRISING A STABILIZED BORONIC ACID COMPOUND BCL6, BCL6B, MCL1 PSMB5 124/4885PSMB8 671/4885PSMB9 175/4885
US-20110059961-A1 4-SUBSTITUTED PYRIDIN-3-YL-CARBOXAMIDE COMPOUNDS AND METHODS OF USE PIM1, PIM3, PIM2 PSMB5 3575/4885PSMB8 4568/4885PSMB9 4664/4885

“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.