Bromide

Bromide

SCHEMBL190865

CN(C)CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

nearest known ligand 0.60

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
▸ CHRM2 known ✓ P08172 1/20 0.39
▸ CHRM4 known ✓ P08173 1/20 0.39
▸ CHRM5 known ✓ P08912 1/20 0.39
▸ CHRM1 known ✓ P11229 1/20 0.39
▸ CHRM3 known ✓ P20309 1/20 0.39
▸ HRH2 known ✓ P25021 1/20 0.39
▸ OPRM1 known ✓ P35372 1/20 0.39
▸ HTR2A P28223 3/20 0.60
▸ HRH1 P35367 3/20 0.60
▸ HIF1A Q16665 1/20 0.54
▸ SIGMAR1 Q99720 1/20 0.46
▸ CYP1A2 P05177 2/20 0.42
▸ CYP2D6 P10635 2/20 0.42
▸ TSHR P16473 2/20 0.42
▸ ALDH1A1 P00352 1/20 0.42
▸ CYP2C19 P33261 1/20 0.42
▸ TAAR1 Q96RJ0 1/20 0.42
▸ LSS P48449 1/20 0.41
▸ CHRNA7 P36544 1/20 0.39
▸ LMNA P02545 1/20 0.39

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
Bromide SCHEMBL246032 0.98 HTR2A (0.58) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Bromide SCHEMBL28158895 0.96 HTR2A (0.56) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Iodide SCHEMBL4110593 0.96 HTR2A (0.60) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Hydrochloric Acid SCHEMBL8861752 0.96 HTR2A (0.60) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Bromide SCHEMBL8909571 0.94 HTR2A (0.53) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Bromide SCHEMBL8782143 0.92 HTR2A (0.52) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Bromide SCHEMBL9147651 0.91 HTR2A (0.50) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Hydrochloric Acid SCHEMBL9549516 0.90 HTR2A (0.53) HTR2AHRH1HIF1ASIGMAR1CYP1A2
Bromide SCHEMBL143506 0.88 HIF1A (0.58) HTR2AHRH1HIF1ACYP1A2CYP2D6
Acetic Acid SCHEMBL9549706 0.86 HTR2A (0.50) HTR2AHRH1HIF1ASIGMAR1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9708284-B2 Process for the preparation of olopatadine and sylil intermediates thereof LABORATORIO CHIMICO INTERNAZIONALE S.P.A. (IT) 2017-07-18 — — US claimed
CN-105849095-A A process for the preparation of olopatadine and sylil intermediates thereof 化学实验室国际股份公司 2016-08-10 — — CN claimed
US-9000195-B2 Process for obtaining olopatadine and intermediates CRYSTAL PHARMA, S.A.U. (ES) 2015-04-07 — — US claimed
EP-2666770-A1 Process for obtaining olopatadine and intermediates Crystal Pharma S.A.U (ES) 2013-11-27 — — EP claimed
EP-2145882-B1 Process for obtaining olopatadine and intermediates CRYSTAL PHARMA SAU (ES) 2013-08-21 — — EP claimed
US-20120004426-A1 PROCESS FOR OBTAINING OLOPATADINE AND INTERMEDIATES RAGACTIVES, S.L.U. (ES) 2012-01-05 — — US claimed
JP-2011528017-A — — 2011-11-10 — — JP claimed
WO-2011128911-A2 IMPROVED PROCESS FOR LL-[(Z)-3-(DIMETHYLAMINO)PROPYIIDENEL-6-LL- DIHYDRODIBENZ[B,EL OXEPIN-2-ACETICACID MSN LABORATORIES LIMITED (IN) 2011-10-20 — — WO claimed
WO-2010007056-A1 PROCESS FOR OBTAINING OLOPATADINE AND INTERMEDIATES RAGACTIVES, S.L.U. (ES) 2010-01-21 — — WO claimed
EP-2145882-A1 Process for obtaining olopatadine and intermediates Ragactives, S.L.U. (ES) 2010-01-20 — — EP claimed
US-6248161-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT-PACKARD COMPANY 2001-06-19 — — US claimed
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-5760809-A INK JET PRINTING XEROX CORPORATION (US) 1998-06-02 — — US claimed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 — — EP claimed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 — — EP 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
EP-0615853-A1 Recording sheets containing phosphonium compounds XEROX CORPORATION (US) 1994-09-21 — — EP claimed

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-20120004426-A1 PROCESS FOR OBTAINING OLOPATADINE AND INTERMEDIATES OXER1, AOC3, OPRD1 CHRM2 29/4885CHRM4 124/4885CHRM5 175/4885

“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.

Send feedback