Bromide

Bromide

SCHEMBL39844

[Br-].[Br-].c1ccc([P+](Cc2ccc(C[P+](c3ccccc3)(c3ccccc3)c3ccccc3)cc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.73

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
SNCA P37840 2/20 0.73
HIF1A Q16665 1/20 0.55
ALDH1A1 P00352 2/20 0.42
CYP3A4 P08684 1/20 0.42
CYP1A2 P05177 2/20 0.41
CYP2D6 P10635 1/20 0.41
TSHR P16473 1/20 0.41
CYP2C19 P33261 1/20 0.41
APP P05067 1/20 0.40
EPHX1 P07099 1/20 0.39
SLC6A2 P23975 2/20 0.36
TAAR1 Q96RJ0 2/20 0.36
MAOA P21397 1/20 0.36
SLC6A4 P31645 1/20 0.36
SLC6A3 Q01959 1/20 0.36
SIGMAR1 Q99720 1/20 0.36
CYP2A6 P11509 1/20 0.36
ADORA2A P29274 1/20 0.36
ADORA1 P30542 1/20 0.36
CALM1 P0DP23 1/20 0.35

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 SCHEMBL2446696 0.95 SNCA (0.69) SNCAHIF1AALDH1A1CYP3A4CYP1A2
Iodide SCHEMBL9321342 0.95 SNCA (0.69) SNCAHIF1AALDH1A1CYP3A4CYP1A2
Bromide SCHEMBL163158 0.95 SNCA (0.67) SNCAHIF1AALDH1A1CYP1A2CYP2D6
Bromide SCHEMBL8331435 0.92 SNCA (0.64) SNCAHIF1AALDH1A1CYP3A4CYP1A2
Phosphine SCHEMBL27584733 0.92 SNCA (0.64) SNCAHIF1AALDH1A1CYP3A4CYP1A2
SCHEMBL29918368 0.92 SNCA (0.65) SNCAHIF1AALDH1A1CYP1A2CYP2D6
Bromide SCHEMBL7728204 0.91 SNCA (0.63) SNCAHIF1AALDH1A1CYP3A4TSHR
Bromide SCHEMBL2648850 0.90 SNCA (0.62) SNCAHIF1AALDH1A1CYP3A4CYP1A2
Bromide SCHEMBL28013112 0.90 SNCA (0.62) SNCAHIF1AALDH1A1CYP3A4CYP1A2
Bromide SCHEMBL28001010 0.90 SNCA (0.62) SNCAHIF1AALDH1A1CYP3A4CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 EP claimed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 EP claimed
US-5817430-A POLYARYLENEVINYLENE POLYMER XEROX CORPORATION (US) 1998-10-06 US claimed
US-5753757-A Electroluminescent polymer compositions and processes thereof XEROX CORPORATION (US) 1998-05-19 US claimed
US-5709976-A Coated papers XEROX CORPORATION (US) 1998-01-20 US claimed
EP-0615853-B1 Recording sheets containing phosphonium compounds XEROX CORP (US) 1996-10-16 EP claimed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 US claimed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 US claimed
CN-114496571-A Method for producing electrolytic capacitor 钰邦科技股份有限公司 2022-05-13 CN disclosed
US-10928728-B2 Photoactivable nitrogen bases BASF SE (DE) 2021-02-23 US disclosed
US-20210033972-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2021-02-04 US disclosed
US-20180217498-A1 PHOTOACTIVABLE NITROGEN BASES BASF SE (DE) 2018-08-02 US disclosed
US-9921477-B2 Photoactivable nitrogen bases BASE SE (DE) 2018-03-20 US disclosed
US-9142782-B2 Organic light-emitting material, device and method CAMBRIDGE DISPLAY TECHNOLOGY, LTD. (GB) 2015-09-22 US disclosed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 US disclosed
EP-0615853-A1 Recording sheets containing phosphonium compounds XEROX CORPORATION (US) 1994-09-21 EP disclosed
EP-0610283-A1 DNA BIS-INTERCALATORS ISIS INNOVATION LIMITED (GB) 1994-08-17 EP disclosed
US-5328961-A Electrically conductive polythiophenecarbonyl polymer networks FORD MOTOR COMPANY (US) 1994-07-12 US disclosed
US-5274046-A Electrically conductive polypyrrolecarbonyl polymer networks FORD MOTOR COMPANY (US) 1993-12-28 US disclosed
WO-1993008165-A1 DNA BIS-INTERCALATORS ISIS INNOVATION LIMITED (GB) 1993-04-29 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-20210033972-A1 PHOTOACTIVABLE NITROGEN BASES CBR1, ARNT, NR0B1 SNCA 2054/4885HIF1A 1258/4885ALDH1A1 1659/4885
US-10928728-B2 Photoactivable nitrogen bases CBR1, NR0B1, NR0B2 SNCA 1887/4885HIF1A 1136/4885ALDH1A1 1733/4885
US-20180217498-A1 PHOTOACTIVABLE NITROGEN BASES CBR1, NR0B1, NR0B2 SNCA 1887/4885HIF1A 1136/4885ALDH1A1 1733/4885

“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.