Bumetanide

Bumetanide

SCHEMBL4018308

CCCCNc1cc(C(=O)O)cc(S(N)(=O)=O)c1Oc1ccccc1.NS(=O)(=O)c1cc(C(=O)O)c(NCc2ccco2)cc1Cl

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC12A1

The experimentally established mechanism targets of Bumetanide. 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
▸ CA2 P00918 3/20 0.67
▸ ALDH1A1 P00352 2/20 0.67
▸ KDM4E B2RXH2 1/20 0.67
▸ USP2 O75604 1/20 0.67
▸ LMNA P02545 1/20 0.67
▸ HPGD P15428 1/20 0.67
▸ TSHR P16473 1/20 0.67
▸ BLM P54132 1/20 0.67
▸ SLC12A2 P55011 1/20 0.67
▸ HIF1A Q16665 1/20 0.67
▸ NPSR1 Q6W5P4 1/20 0.67
▸ HSD17B10 Q99714 1/20 0.67
▸ CISD1 Q9NZ45 9/20 0.64
▸ CA12 O43570 2/20 0.64
▸ CA1 P00915 2/20 0.64
▸ CA6 P23280 2/20 0.64
▸ CA5A P35218 2/20 0.64
▸ CA7 P43166 2/20 0.64
▸ CA9 Q16790 2/20 0.64
▸ CA14 Q9ULX7 2/20 0.64

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
SCHEMBL11788072 0.84 ALDH1A1 (0.64) CA2ALDH1A1KDM4EUSP2LMNA
SCHEMBL19300067 0.83 ALDH1A1 (0.61) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL27525 0.82 KDM4E (1.00) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL29388271 0.82 KDM4E (1.00) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL4425232 0.82 KDM4E (1.00) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL23455698 0.81 KDM4E (0.98) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL2255359 0.81 KDM4E (0.98) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL6239781 0.81 KDM4E (0.98) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL251062 0.81 KDM4E (0.98) CA2ALDH1A1KDM4EUSP2LMNA
Bumetanide SCHEMBL28661289 0.81 KDM4E (0.98) CA2ALDH1A1KDM4EUSP2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103717597-B Heterocyclic compounds as kinase inhibitors 原真股份有限公司 2017-07-04 — — CN disclosed
CN-103492389-B Pyrazolo [4,3-d] pyrimidine as inhibitors of kinases 原真股份有限公司 2016-09-14 — — CN disclosed
EP-1414845-A4 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES (US) 2009-07-08 — — EP disclosed
EP-1404702-A4 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES INC (US) 2009-07-08 — — EP disclosed
EP-1379132-A4 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES (US) 2009-07-01 — — EP disclosed
EP-1951702-A2 DIURETIC-LIKE COMPOUND ANALOGS USEFUL FOR REGULATION OF CENTRAL NERVOUS SYSTEM DISORDERS NeuroTherapeutics Pharma, Inc. (US) 2008-08-06 — — EP disclosed
EP-1937242-A2 METHODS AND COMPOSITIONS FOR THE TREATMENT OF NEUROPSYCHIATRIC AND ADDICTIVE DISORDERS NeuroTherapeutics Pharma, Inc. (US) 2008-07-02 — — EP disclosed
WO-2007047447-A2 DIURETIC-LIKE COMPOUND ANALOGS USEFUL FOR REGULATION OF CENTRAL NERVOUS SYSTEM DISORDERS NEUROTHERAPEUTICS PHARMA, INC. (US) 2007-04-26 — — WO disclosed
WO-2007047698-A2 METHODS AND COMPOSITIONS FOR THE TREATMENT OF NEUROPSYCHIATRIC AND ADDICTIVE DISORDERS NEUROTHERAPEUTICS PHARMA, INC. (US) 2007-04-26 — — WO disclosed
US-20050038072-A1 Nitrogeneous cyclic ketone derivative, process for producing the same, and use TAKEDA CHEMICAL INDUSTRIES, LTD. 2005-02-17 — — US disclosed
EP-1460062-A1 NITROGENOUS CYCLIC KETONE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE Takeda Chemical Industries, Ltd. (JP) 2004-09-22 — — EP disclosed
EP-1414845-A2 HUMAN SECRETED PROTEINS Human Genome Sciences (US) 2004-05-06 — — EP disclosed
EP-1404702-A2 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES, INC. (US) 2004-04-07 — — EP disclosed
EP-1385381-A2 HUMAN SECRETED PROTEINS Human Genome Sciences, Inc. (US) 2004-02-04 — — EP disclosed
EP-1379132-A2 HUMAN SECRETED PROTEINS Human Genome Sciences (US) 2004-01-14 — — EP disclosed
WO-2003004623-A2 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES, INC. (US) 2003-01-16 — — WO disclosed
WO-2003004622-A2 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES, INC. (US) 2003-01-16 — — WO disclosed
WO-2003000865-A2 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES, INC. (US) 2003-01-03 — — WO disclosed
WO-2002102994-A2 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES, INC. (US) 2002-12-27 — — WO disclosed
WO-2002095010-A2 HUMAN SECRETED PROTEINS HUMAN GENOME SCIENCES, INC. (US) 2002-11-28 — — 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 (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-20050038072-A1 Nitrogeneous cyclic ketone derivative, process for producing the same, and use BDKRB1, BDKRB2, TACR1 CA2 1578/4885ALDH1A1 1984/4885KDM4E 2064/4885

“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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