Bromide

Bromide

SCHEMBL2647553

FC(F)(F)c1cccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1.[Br-]

nearest known ligand 0.54

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 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 2/20 0.54
HTR2B P41595 2/20 0.54
HTR2C P28335 1/20 0.54
ACP3 P15309 2/20 0.50
TAAR1 Q96RJ0 1/20 0.49
SIGMAR1 Q99720 2/20 0.48
TP53 P04637 1/20 0.48
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2D6 P10635 1/20 0.48
TSHR P16473 1/20 0.48
CYP2C19 P33261 1/20 0.48
SLC6A4 P31645 2/20 0.48
MAPT P10636 2/20 0.48
LMNA P02545 1/20 0.48
ADRA2C P18825 1/20 0.48
ADRA1A P35348 1/20 0.48
DRD3 P35462 1/20 0.48
OPRK1 P41145 1/20 0.48
IDO1 P14902 2/20 0.47

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 SCHEMBL7782825 0.97 HTR2A (0.54) HTR2AHTR2BHTR2CACP3TAAR1
Bromide SCHEMBL9538904 0.86 SNCA (0.46) HTR2AHTR2BHTR2CSNCA
Iodide SCHEMBL16398702 0.83 TACR1 (0.45) HTR2AHTR2BHTR2CSNCA
Bromide SCHEMBL6524406 0.82 SNCA (0.55) TAAR1SIGMAR1CYP1A2CYP2D6TSHR
Bromide SCHEMBL1840962 0.81 SNCA (0.56) ACP3TAAR1TSHRMAPTIDO1
Bromide SCHEMBL29255353 0.80 HTR2A (0.62) HTR2AHTR2BHTR2CACP3TAAR1
Hydrochloric Acid SCHEMBL5149449 0.78 SNCA (0.52) TAAR1SIGMAR1CYP1A2CYP2D6TSHR
Bromide SCHEMBL1352977 0.77 SNCA (0.47) TAAR1IDO1PPARGPPARAMEN1
Hydrochloric Acid SCHEMBL9419870 0.77 SNCA (0.53) ACP3TAAR1TSHRMAPTIDO1
Bromide SCHEMBL163158 0.75 SNCA (0.67) TAAR1SIGMAR1CYP1A2CYP2D6TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114249718-A Sulfonium salt derivative and preparation method and medical application thereof 中国药科大学 2022-03-29 CN claimed
CN-114249718-B Sulfonium salt derivative, preparation method and medical application thereof 中国药科大学 2023-09-22 CN disclosed
CN-114249718-A Sulfonium salt derivative and preparation method and medical application thereof 中国药科大学 2022-03-29 CN disclosed
EP-3426634-A1 DISUBTITUTED AZETIDINES, PYRROLIDINES, PIPERIDINES AND AZEPANES AS INHIBITORS OF MONOAMINE OXIDASE B FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES University of Ljubljana (SI) 2019-01-16 EP disclosed
WO-2018055096-A1 DISUBTITUTED AZETIDINES, PYRROLIDINES, PIPERIDINES AND AZEPANES AS INHIBITORS OF MONOAMINE OXIDASE B FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES UNIVERSITY OF LJUBLJANA (SI) 2018-03-29 WO disclosed
US-8722709-B2 Mineralocorticoid receptor antagonists BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2014-05-13 US disclosed
EP-2638012-A1 PYRIDYL UREAS AS MINERALOCORTICOID RECEPTOR ANTAGONISTS Boehringer Ingelheim International GmbH (DE) 2013-09-18 EP disclosed
US-20120289551-A1 MINERALOCORTICOID RECEPTOR ANTAGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH 2012-11-15 US disclosed
WO-2012064631-A1 PYRIDYL UREAS AS MINERALOCORTICOID RECEPTOR ANTAGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-05-18 WO disclosed
EP-0818197-B1 Heterocyclic condensed pyridines as CETP inhibitors BAYER AG (DE) 2003-11-12 EP disclosed
EP-0968162-A1 5-HYDROXYALKYL SUBSTITUTED PHENYLS AND THEIR USE IN MEDICAMENTS FOR THE TREATMENT OF ARTERIOSCLEROSIS AND HYPERLIPOPROTEINAEMIA BAYER AG (DE) 2000-01-05 EP disclosed
EP-0934274-A1 SUBSTITUTED PYRIDINES AND BIPHENYLS AS ANTI-HYPERCHOLESTERINEMIC, ANTI-HYPERLIPOPROTEINEMIC AND ANTI-HYPERGLYCEMIC AGENTS Bayer Corporation (US) 1999-08-11 EP disclosed
US-5932587-A FOR TREATMENT OF DISLIPIDAEMIA, ARTERIOSCLEROSIS BAYER AKTIENGESELLSCHAFT (DE) 1999-08-03 US disclosed
US-5925645-A ARTERIOSCLEROSIS BAYER AKTIENGESELLSCHAFT (DE) 1999-07-20 US disclosed
WO-1998034895-A1 5-HYDROXYALKYL SUBSTITUTED PHENYLS AND THEIR USE IN MEDICAMENTS FOR THE TREATMENT OF ARTERIOSCLEROSIS AND HYPERLIPOPROTEINAEMIA BAYER AKTIENGESELLSCHAFT (DE) 1998-08-13 WO disclosed
EP-0825185-A1 Pyridine fused to a bicyclic ring BAYER AG (DE) 1998-02-25 EP disclosed
WO-1998004528-A2 SUBSTITUTED PYRIDINES AND BIPHENYLS AS ANTI-HYPERCHOLESTERINEMIC, ANTI-HYPERLIPOPROTEINEMIC AND ANTI-HYPERGLYCEMIC AGENTS BAYER CORPORATION (US) 1998-02-05 WO disclosed
EP-0818197-A1 Heterocyclic condensed pyridines as CETP inhibitors BAYER AG (DE) 1998-01-14 EP disclosed
EP-0796846-A1 2-Aryl substituted pyridines BAYER AG (DE) 1997-09-24 EP disclosed
US-5266593-A Substituted pyran derivatives having antiinfective activity E. R. SQUIBB & SONS, INC. (US) 1993-11-30 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 (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-20120289551-A1 MINERALOCORTICOID RECEPTOR ANTAGONISTS NR3C2, MC2R, AVPR2 HTR2A 324/4885HTR2B 357/4885HTR2C 302/4885

“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.