Bromide

Bromide

SCHEMBL9192803

CCN1C(=CC(C)=Cc2sc3ccccc3[n+]2CC)Sc2ccccc21.[Br-]

nearest known ligand 0.98

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
▸ NSD2 O96028 1/20 0.98
▸ ALDH1A1 P00352 6/20 0.96
▸ MEN1 O00255 5/20 0.96
▸ KMT2A Q03164 5/20 0.96
▸ HTT P42858 5/20 0.96
▸ RAB9A P51151 5/20 0.96
▸ BLM P54132 4/20 0.96
▸ NPC1 O15118 4/20 0.96
▸ MAPT P10636 4/20 0.96
▸ POLB P06746 3/20 0.96
▸ APAF1 O14727 2/20 0.96
▸ THRB P10828 2/20 0.96
▸ PKM P14618 2/20 0.96
▸ RECQL P46063 2/20 0.96
▸ SMN1; SMN2 Q16637 2/20 0.96
▸ NPSR1 Q6W5P4 2/20 0.96
▸ TDP1 Q9NUW8 2/20 0.96
▸ PLA2G1B P04054 1/20 0.96
▸ MAPK1 P28482 1/20 0.96
▸ CDK5 Q00535 1/20 0.96

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 SCHEMBL29362921 1.00 NSD2 (0.98) NSD2ALDH1A1MEN1KMT2AHTT
SCHEMBL29349411 0.99 NSD2 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
SCHEMBL2409472 0.99 NSD2 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
SCHEMBL6426499 0.99 NSD2 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
SCHEMBL10035965 0.99 NSD2 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
Iodide SCHEMBL145357 0.98 MEN1 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
Iodide SCHEMBL5500973 0.98 MEN1 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
Iodide SCHEMBL145356 0.98 MEN1 (1.00) NSD2ALDH1A1MEN1KMT2AHTT
Hydrochloric Acid SCHEMBL9015126 0.98 NSD2 (0.98) NSD2ALDH1A1MEN1KMT2AHTT
Bromide SCHEMBL10431222 0.90 NSD2 (0.80) NSD2ALDH1A1MEN1KMT2AHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-3958991-A PHOTOCONDUCTOR EASTMAN KODAK COMPANY (US) 1976-05-25 — — US claimed
EP-0333435-B1 High contrast photographic element and emulsion and process for their use EASTMAN KODAK CO (US) 1995-12-13 — — EP disclosed
EP-0345025-B1 High contrast photographic recording material and emulsion and process for their development EASTMAN KODAK CO (US) 1994-03-09 — — EP disclosed
US-5126227-A High speed, low fogging, quality, efficiency EASTMAN KODAK COMPANY (US) 1992-06-30 — — US disclosed
US-5104769-A Negative working silver halide and arylhydrazide nucleating agent EASTMAN KODAK COMPANY (US) 1992-04-14 — — US disclosed
US-5041355-A High contrast photographic element including an aryl sulfonamidophenyl hydrazide containing ethyleneoxy groups EASTMAN KODAK COMPANY (US) 1991-08-20 — — US disclosed
US-4994365-A Nucleating agents EASTMAN KODAK COMPANY (US) 1991-02-19 — — US disclosed
US-4988604-A Silver halide elements for development with alkaline agent, multilayer, nucleation agent EASTMAN KODAK COMPANY (US) 1991-01-29 — — US disclosed
US-4975354-A Silver halide developed in presence of a hydrazone using an aqueous alkaline solution; black and white photography; lithography EASTMAN KODAK COMPANY (US) 1990-12-04 — — US disclosed
EP-0209012-B1 HIGH CONTRAST PHOTOGRAPHIC ELEMENTS EXHIBITING REDUCED PEPPER FOG EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1990-11-07 — — EP disclosed
US-4560638-A Halftone imaging silver halide emulsions, photographic elements, and processes which employ novel arylhydrazides EASTMAN KODAK COMPANY (US) 1985-12-24 — — US disclosed
US-4304769-A PESTICIDES EASTMAN KODAK COMPANY (US) 1981-12-08 — — US disclosed
US-4247627-A Photographic elements having hydrophilic colloid layers containing hydrophobic ultraviolet absorbers uniformly loaded in latex polymer particles EASTMAN KODAK COMPANY (US) 1981-01-27 — — US disclosed
US-4214047-A Photographic elements having hydrophilic colloid layers containing hydrophobic addenda uniformly loaded in latex polymer particles EASTMAN KODAK COMPANY (US) 1980-07-22 — — US disclosed
US-4203716-A Photographic elements having hydrophilic colloid layers containing hydrophobic addenda uniformly loaded in latex polymer particles EASTMAN KODAK COMPANY (US) 1980-05-20 — — US disclosed
US-4199363-A Processes for achieving uniform, efficient distribution of hydrophobic materials through hydrophilic colloid layers and loaded latex compositions EASTMAN KODAK COMPANY (US) 1980-04-22 — — US disclosed
US-4097284-A TRIMETHINECYANINE DYE AND A NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING A MERCAPTO FUJI PHOTO FILM CO., LTD. (JA) 1978-06-27 — — US disclosed
US-4004572-A Solar energy collection and retrieval employing reversible photochemical isomerization BATTELLE DEVELOPMENT CORPORATION (US) 1977-01-25 — — US disclosed
US-4004573-A Process and apparatus for solar energy collection and retrieval BATTELLE DEVELOPMENT CORPORATION (US) 1977-01-25 — — US disclosed
US-3979213-A METHINE DYES GILMAN JR PAUL B 1976-09-07 — — US disclosed
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