Bromide

Bromide

SCHEMBL2521169

CC(Br)c1ccccc1.CCCCC(CCCC)c1ccnc(-c2cc(C(CCCC)CCCC)ccn2)c1.[Br-].[Br-].[Fe+2]

nearest known ligand 0.35

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
OPRM1 known ✓ P35372 1/20 0.31
POLB P06746 2/20 0.35
ALDH1A1 P00352 2/20 0.35
MAPT P10636 1/20 0.35
KDM4C Q9H3R0 2/20 0.33
KDM5A P29375 1/20 0.32
KDM5B Q9UGL1 1/20 0.32
PDE4D Q08499 1/20 0.31
PTGES O14684 2/20 0.31
ALOX5 P09917 2/20 0.31
PPARG P37231 2/20 0.31
KDM4A O75164 1/20 0.31
OPRD1 P41143 1/20 0.31
OPRK1 P41145 1/20 0.31
OPRL1 P41146 1/20 0.31
CYP17A1 P05093 1/20 0.31
KDM4E B2RXH2 1/20 0.31
TACR3 P29371 1/20 0.31
CYP1A2 P05177 1/20 0.31
CYP2D6 P10635 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
Bromide SCHEMBL2514869 0.86 CCR1 (0.35) POLBALDH1A1MAPTKDM5AKDM5B
SCHEMBL175672 0.83 CCR1 (0.38) POLBALDH1A1MAPTKDM5AKDM5B
SCHEMBL145233 0.78 CCR1 (0.33) POLBALDH1A1MAPTCYP1A2CYP2D6
SCHEMBL174988 0.77 NR1I2 (0.39) KDM5AKDM4E
SCHEMBL3040111 0.77 NR1I2 (0.39) POLBALDH1A1MAPTKDM4CKDM5A
SCHEMBL13039644 0.76 LNPEP (0.37) MAPTKDM4ETDP1
SCHEMBL2511650 0.74 KDM5A (0.35) POLBALDH1A1KDM4CKDM5AKDM5B
SCHEMBL5974098 0.72 NR1I2 (0.47) KDM5AKDM4E
Chloromethane SCHEMBL6909514 0.71 CYP1A2 (0.38) POLBKDM4ECYP1A2CYP2D6CYP19A1
SCHEMBL6682502 0.70 POLB (0.47) POLBALDH1A1MAPTOPRM1OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8034971-B2 Method for producing 1,2-phenylethane compound using atom transfer radical coupling reaction NIPPON SODA CO., LTD. (JP) 2011-10-11 US disclosed
US-20090275772-A1 Metrod for Producing 1,2-Phenylethane Compound Using Atom Transfer Radical Coupling Reaction NIPPON SODA CO., LTD. (JP) 2009-11-05 US disclosed
US-7579401-B2 Block polymer of polymethoxypolyethylene glycol monomethyl methacrylate and polystyrene; LiClO4 a lithium salt as electrolyte; living copolymerization, block polymerization; excellent thermal characteristics, physical characteristics, and ionic conductivity; secondary batteries NIPPON SODA CO., LTD. (JP) 2009-08-25 US disclosed
EP-1997798-A1 METHOD FOR PRODUCING 1,2-PHENYLETHANE COMPOUND USING ATOM TRANSFER RADICAL COUPLING REACTION Nippon Soda Co., Ltd. (JP) 2008-12-03 EP disclosed
EP-1553117-B1 SOLID POLYMER ELECTROLYTE NIPPON SODA CO (JP) 2007-01-17 EP disclosed
US-20050256256-A1 Block polymer of polymethoxypolyethylene glycol monomethyl methacrylate and polystyrene; LiClO4 a lithium salt as electrolyte; living copolymerization, block polymerization; excellent thermal characteristics, physical characteristics, and ionic conductivity; secondary batteries NIPPON SODA CO., LTD (JP) 2005-11-17 US disclosed
EP-1553117-A1 SOLID POLYMER ELECTROLYTE NIPPON SODA CO., LTD. (JP) 2005-07-13 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-20090275772-A1 Metrod for Producing 1,2-Phenylethane Compound Using Atom Transfer Radical Coupling Reaction ROS1, MET, MT-CO1 OPRM1 772/4885POLB 1242/4885ALDH1A1 74/4885

“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.