Bromide

Bromide

SCHEMBL8053180

Cc1ccccc1[P+](Cc1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

nearest known ligand 0.47

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 0.47
HIF1A Q16665 1/20 0.40
SCN4A P35499 2/20 0.36
TAAR1 Q96RJ0 4/20 0.35
SLC6A2 P23975 2/20 0.35
SIGMAR1 Q99720 2/20 0.35
MAOA P21397 1/20 0.35
SLC6A4 P31645 1/20 0.35
SLC6A3 Q01959 1/20 0.35
CYP2A6 P11509 1/20 0.35
ADORA2A P29274 1/20 0.35
ADORA1 P30542 1/20 0.35
CYP1A2 P05177 1/20 0.34
TRAP1 Q12931 1/20 0.34
SLC18A2 Q05940 1/20 0.33
CYP2D6 P10635 1/20 0.33
EPHX1 P07099 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
ALDH1A1 P00352 1/20 0.33
LMNA P02545 1/20 0.33

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 SCHEMBL9850761 0.96 SNCA (0.44) SNCAHIF1ASCN4ATAAR1SLC6A2
Hydrochloric Acid SCHEMBL28196291 0.93 SNCA (0.42) SNCAHIF1ASCN4ATAAR1SLC6A2
Hydrochloric Acid SCHEMBL11410207 0.93 SNCA (0.44) SNCAHIF1ASCN4ATAAR1SLC6A2
Bromide SCHEMBL6060755 0.90 SNCA (0.39) SNCASCN4ATAAR1SLC6A2SIGMAR1
Iodide SCHEMBL6060968 0.86 TAAR1 (0.39) SNCASCN4ATAAR1SLC6A2SIGMAR1
Hydrochloric Acid SCHEMBL6060719 0.86 TAAR1 (0.39) SNCASCN4ATAAR1SLC6A2SIGMAR1
Hydrochloric Acid SCHEMBL28678048 0.84 SNCA (0.41) SNCAHIF1ASCN4ATAAR1SLC6A2
Bromide SCHEMBL163158 0.80 SNCA (0.67) SNCAHIF1ATAAR1SLC6A2SIGMAR1
Bromide SCHEMBL7197753 0.79 SNCA (0.37) SNCATAAR1CYP2A6CYP1A2LMNA
Phosphoric Acid SCHEMBL7195799 0.79 LAP3 (0.40) L3MBTL1ALDH1A1LMNANPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11319276-B2 Preparation of diesters of (meth)acrylic acid from epoxides EVONIK OPERATIONS GMBH (DE) 2022-05-03 US disclosed
US-10676571-B2 Polyetherimides with improved melt stability SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2020-06-09 US disclosed
EP-3652141-A1 PREPARATION OF DIESTERS OF (METH)ACRYLIC ACID FROM EPOXIDES Evonik Degussa GmbH (DE) 2020-05-20 EP disclosed
WO-2020035561-A1 PREPARATION OF DIESTERS OF (METH)ACRYLIC ACID FROM EPOXIDES EVONIK OPERATIONS GMBH (DE) 2020-02-20 WO disclosed
EP-2904032-B1 METHODS OF MANUFACTURE OF BIS(PHTHALIMIDE)S AND POLYETHERIMIDES, AND BIS(PHTHALIMIDE)S, AND POLYETHERIMIDES FORMED THEREFROM SABIC GLOBAL TECHNOLOGIES BV (NL) 2018-03-07 EP disclosed
EP-3077445-A1 POLYETHERIMIDES WITH IMPROVED MELT STABILITY SABIC Global Technologies B.V. (NL) 2016-10-12 EP disclosed
WO-2016033156-A1 IRON-CATALYZED OXIDATIVE POLYMERIZATION OF PHENOLS SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2016-03-03 WO disclosed
EP-2904032-A2 METHODS OF MANUFACTURE OF BIS(PHTHALIMIDE)S AND POLYETHERIMIDES, AND BIS(PHTHALIMIDE)S, AND POLYETHERIMIDES FORMED THEREFROM SABIC Global Technologies B.V. (NL) 2015-08-12 EP disclosed
WO-2015084781-A1 POLYETHERIMIDES WITH IMPROVED MELT STABILITY SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2015-06-11 WO disclosed
US-20150152224-A1 POLYETHERIMIDES WITH IMPROVED MELT STABILITY SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2015-06-04 US disclosed
US-20140099510-A1 METHODS OF MANUFACTURE OF BIS(PHTHALIMIDE)S AND POLYETHERIMIDES, AND BIS(PHTHALIMIDE)S, AND POLYETHERIMIDES FORMED THEREFROM SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2014-04-10 US disclosed
WO-2014055856-A2 METHODS OF MANUFACTURE OF BIS(PHTHALIMIDE)S AND POLYETHERIMIDES, AND BIS(PHTHALIMIDE)S, AND POLYETHERIMIDES FORMED THEREFROM SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2014-04-10 WO disclosed
EP-1021426-A4 CATALYTIC ASYMMETRIC EPOXIDATION UNIV COLORADO STATE RES FOUND (US) 2000-07-26 EP disclosed
EP-1021426-A1 CATALYTIC ASYMMETRIC EPOXIDATION COLORADO STATE UNIVERSITY RESEARCH FOUNDATION (US) 2000-07-26 EP disclosed
WO-1998015544-A1 CATALYTIC ASYMMETRIC EPOXIDATION COLORADO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1998-04-16 WO disclosed
EP-0220810-A1 Insecticidal ethers IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1987-05-06 EP 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-11319276-B2 Preparation of diesters of (meth)acrylic acid from epoxides MMAB, EPHX2, MTHFD2 SNCA 4528/4885HIF1A 246/4885SCN4A 4555/4885

“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.