Bromide

Bromide

SCHEMBL3389414

[Br-].c1ccc([P+](c2ccccc2)(c2ccccc2)C2CCC2)cc1

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 2/20 0.35
SLC18A2 Q05940 1/20 0.34
CYP1A2 P05177 1/20 0.32
CYP2D6 P10635 1/20 0.32
GAA P10253 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.32
RECQL P46063 1/20 0.32
CA1 P00915 1/20 0.32
IDO1 P14902 1/20 0.31

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
Hydrochloric Acid SCHEMBL7631802 0.95 HIF1A (0.35) HIF1ASLC18A2CYP1A2CYP2D6GAA
Bromide SCHEMBL2447458 0.95 GAA (0.36) HIF1ACYP2D6GAAL3MBTL1IDO1
Iodide SCHEMBL7626801 0.95 HIF1A (0.35) HIF1ASLC18A2CYP1A2CYP2D6GAA
Bromide SCHEMBL7633092 0.93 IDO1 (0.38) HIF1AGAAL3MBTL1IDO1
Bromide SCHEMBL2445980 0.93 IDO1 (0.38) HIF1AGAAL3MBTL1IDO1
Bromide SCHEMBL3322091 0.93 IDO1 (0.38) HIF1AGAAL3MBTL1IDO1
SCHEMBL31321441 0.92 GAA (0.38) HIF1ACYP2D6GAAL3MBTL1IDO1
Bromide SCHEMBL1082615 0.92 HIF1A (0.36) HIF1AIDO1
Bromide SCHEMBL10533526 0.91 IDO1 (0.37) HIF1ACYP1A2GAAL3MBTL1IDO1
Iodide SCHEMBL6591776 0.90 GAA (0.36) HIF1ACYP2D6GAAL3MBTL1IDO1

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9481828-B2 Liquid Crystal compound containing cyclobutyl group and difluoromethyleneoxy linking group, and preparation method and use thereof SHIJIAZHUANG CHENGZHI YONGHUA DISPLAY MATERIAL CO., LTD. (CN) 2016-11-01 US disclosed
US-20150284632-A1 Liquid Crystal Compound Containing Cyclobutyl Group and Difluoromethyleneoxy Linking Group, and Preparation Method and Use Thereof SHIJIAZHUANG CHENGZHI YONGHUA DISPLAY MATERIALS CO., LTD. (CN) 2015-10-08 US disclosed
US-8455466-B2 Vitamin d analogues, compositions comprising said analogues and their use LEO PHARMA A/S (DK) 2013-06-04 US disclosed
EP-1556345-B1 VITAMIN D ANALOGUES, COMPOSITIONS COMPRISING SAID ANALOGUES AND THEIR USE LEO PHARMA AS (DK) 2010-12-15 EP disclosed
US-20060166949-A1 Vitamin d analogues, compositions comprising said analogues and their use LEO PHARMA A/S (DE) 2006-07-27 US disclosed
CN-1705643-A Vitamin D analogues, compositions comprising said analogues and their use LEO PHARMA AS (DK) 2005-12-07 CN disclosed
EP-1556345-A1 VITAMIN D ANALOGUES, COMPOSITIONS COMPRISING SAID ANALOGUES AND THEIR USE Leo Pharma A/S (DK) 2005-07-27 EP disclosed
WO-2004037781-A1 VITAMIN D ANALOGUES, COMPOSITIONS COMPRISING SAID ANALOGUES AND THEIR USE LEO PHARMA A/S (DK) 2004-05-06 WO disclosed
EP-0780452-B1 Aqueous paint TOYO SEIKAN KAISHA LTD (JP) 2002-03-06 EP disclosed
US-5763507-A EPOXY ACRYLATE RESIN TOYO SEIKAN KAISHA, LTD. (JP) 1998-06-09 US disclosed
EP-0780452-A2 Aqueous paint TOYO SEIKAN KAISHA LIMITED (JP) 1997-06-25 EP disclosed
US-5310854-A Solvent, coatings for beverage cans THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
EP-0329021-B1 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds DOW CHEMICAL CO (US) 1994-01-26 EP disclosed
US-5206312-A Polysiloxanes hydrosilated with unsaturated aromatic alcohols and siloxy-containing compounds having hydroxy groups to advance polyepoxides and epoxy resins; electronics; coatings; composites THE DOW CHEMICAL COMPANY (US) 1993-04-27 US disclosed
WO-1991016888-A1 SPIRO[BENZOFURANCYCLOALKANE]CARBOXAMIDES AS 5HT3 ANTAGONISTS RHONE-POULENC RORER INTERNATIONAL (HOLDINGS), INC. (US) 1991-11-14 WO disclosed
EP-0329021-A2 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-08-23 EP disclosed
US-4808692-A Preparation of advanced epoxy resins from epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-02-28 US disclosed
US-4206140-A INSECTICIDES, ANTHELMINTICS ROUSSEL UCLAF (FR) 1980-06-03 US disclosed
US-4101574-A Cyclopropanecarboxylic acid chlorides ROUSSEL UCLAF (FR) 1978-07-18 US disclosed
US-3997586-A Cyclopropanecarboxylic acids and esters ROUSSEL-UCLAF (FR) 1976-12-14 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 (2 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-20150284632-A1 Liquid Crystal Compound Containing Cyclobutyl Group and Difluoromethyleneoxy Linking Group, and Preparation Method and Use Thereof CFB, CFL1, FASTKD1 HIF1A 4619/4885SLC18A2 4136/4885CYP1A2 1641/4885
US-20060166949-A1 Vitamin d analogues, compositions comprising said analogues and their use VDR, CYP2R1, CYP24A1 HIF1A 1273/4885SLC18A2 3621/4885CYP1A2 117/4885

“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.