Bromide

Bromide

SCHEMBL7873025

Cc1ccccc1[P+](c1ccccc1C)(c1ccccc1C)c1ccccc1C.[Br-]

nearest known ligand 0.50

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
ACHE known ✓ P22303 3/20 0.50
TSHR P16473 4/20 0.50
ALDH1A1 P00352 4/20 0.39
CA1 P00915 2/20 0.39
CA2 P00918 2/20 0.39
CA7 P43166 2/20 0.39
CA9 Q16790 2/20 0.39
ESR1 P03372 1/20 0.39
CYP3A4 P08684 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
CYP1A2 P05177 2/20 0.36
CYP2A6 P11509 2/20 0.36
MAPT P10636 1/20 0.33
HTT P42858 1/20 0.33
LMNA P02545 1/20 0.33
ALOX12 P18054 1/20 0.33
TAAR1 Q96RJ0 1/20 0.32
HSD17B10 Q99714 1/20 0.32
MAOA P21397 1/20 0.31
MAOB P27338 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
SCHEMBL30634705 0.97 TSHR (0.53) TSHRACHEALDH1A1CA1CA2
Fluoride Ion SCHEMBL943596 0.94 TSHR (0.50) TSHRACHEALDH1A1CA1CA2
Hydrochloric Acid SCHEMBL11444635 0.94 TSHR (0.50) TSHRACHEALDH1A1CA1CA2
Water SCHEMBL4384424 0.94 TSHR (0.50) TSHRACHEALDH1A1CA1CA2
SCHEMBL7874669 0.92 TSHR (0.47) TSHRACHEALDH1A1CA1CA2
Bromide SCHEMBL7886102 0.85 TSHR (0.41) TSHRACHEALDH1A1CA1CA2
SCHEMBL7874600 0.85 ACHE (0.41) TSHRACHEALDH1A1CA1CA2
Phenol SCHEMBL7872892 0.83 TSHR (0.39) TSHRACHEALDH1A1CA1CA2
Acetic Acid SCHEMBL1033265 0.81 ALDH1A1 (0.41) TSHRACHEALDH1A1CA1TDP1
Bromide SCHEMBL9067697 0.80 TSHR (0.47) TSHRACHEALDH1A1CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6316575-B1 MELT TRANSESTERIFICATION OF DIOL COMPOUND AND CARBOANTE COMPOUND USING CATALYST COMPRISING A PHOSPHORUS-CONTAINING BASIC COMPOUND QUATERNARY PHOSPHONIUM SALT TO FORM POLYCARBONATE IDEMITSU KOSAN CO., LTD. (JP) 2001-11-13 US claimed
US-5837425-A PRESENSITIZATION OF PLATES, SUPPORTS, MULTILAYER, EXPOSURE TO ACTINIC RADIATION OF FILMS, DEVELOPMENT OF PLATES WITH ALKALI FUJI PHOTO FILM CO., LTD. (JP) 1998-11-17 US disclosed
EP-0716347-A1 Developer for photosensitive lithographic printing plate FUJI PHOTO FILM CO., LTD. (JP) 1996-06-12 EP disclosed
EP-0516372-B1 Concentrated dampening water composition for lithographic printing FUJI PHOTO FILM CO LTD (JP) 1996-04-24 EP disclosed
US-5221330-A Hydrophilic film-forming polymer, buffer, water miscible organic solvent, micelle-forming compound, water FUJI PHOTO FILM CO., LTD. (JP) 1993-06-22 US disclosed
EP-0516372-A1 Concentrated dampening water composition for lithographic printing FUJI PHOTO FILM CO., LTD. (JP) 1992-12-02 EP disclosed