Bromide

Bromide

SCHEMBL3203566

[Br-].[Cu+].[Cu]

nearest known ligand 0.00

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL118850 0.82
Bromide SCHEMBL3725335 0.82
Bromide SCHEMBL449 0.82
Bromide SCHEMBL360044 0.82
Bromide SCHEMBL3378419 0.67
Bromide SCHEMBL5672745 0.67
Bromide SCHEMBL11786078 0.67
Hydrochloric Acid SCHEMBL4185254 0.67
SCHEMBL1505844 0.67
Bromide SCHEMBL8112164 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109232887-A A kind of shape-memory polymer and preparation method thereof that crosslinking points are controllable 中国科学院成都有机化学有限公司 2019-01-18 CN claimed
CN-109232887-A A kind of shape-memory polymer and preparation method thereof that crosslinking points are controllable 中国科学院成都有机化学有限公司 2019-01-18 CN disclosed
US-7678869-B2 Atom or group transfer radical polymerization CARNEGIE MELLON UNIVERSITY (US) 2010-03-16 US disclosed
US-20060258826-A1 Atom or group transfer radical polymerization CARNEGIE MELLON UNIVERSITY 2006-11-16 US disclosed
EP-0966489-B1 IMPROVEMENTS IN ATOM OR GROUP TRANSFER RADICAL POLYMERIZATION UNIV CARNEGIE MELLON (US) 2006-11-15 EP disclosed
US-7125938-B2 Atom or group transfer radical polymerization CARNEGIE MELLON UNIVERSITY (US) 2006-10-24 US disclosed
US-20040204556-A1 Atom or group transfer radical polymerization MATYJASZEWSKI KRZYSZTOF (US) 2004-10-14 US disclosed
US-6541580-B1 Controlling living polymerization via e.g. polyphosphazene initiators CARNEGIE MELLON UNIVERSITY 2003-04-01 US disclosed
US-6512060-B1 Contacting at least one first molecule comprising one or more radically transferable atoms or groups, and at least one second molecule comprising one or more radically transferable atoms or groups with a system comprising: a transition metal, CARNEGIE MELLON UNIVERSITY 2003-01-28 US disclosed
US-5214044-A Antiallergens PFIZER INC. (US) 1993-05-25 US disclosed
US-5120747-A Antiallergens, antiinflammatory agent PFIZER INC. (US) 1992-06-09 US disclosed
EP-0470078-A1 1,4-DIHYDROPYRIDINES Pfizer Limited (GB) 1992-02-12 EP disclosed
US-5070205-A Chemical intermediate for anticoagulants PFIZER INC. (US) 1991-12-03 US disclosed
EP-0310386-B1 4-ARYL-5-CARBAMOYL-1,4-DIHYDROPYRIDINES Pfizer Limited (GB) 1991-11-06 EP disclosed
US-5063237-A Antiallergens and antiinflammatory agents PFIZER INC. (US) 1991-11-05 US disclosed
US-4963560-A ANTIALLERGENS, ANTIINFLAMMATORY AGENTS PFIZER INC. (US) 1990-10-16 US disclosed
WO-1990011280-A1 1,4-DIHYDROPYRIDINES PFIZER LIMITED (GB) 1990-10-04 WO disclosed
US-4935430-A Platelet activating factor antagonists PFIZER INC. (US) 1990-06-19 US disclosed
EP-0365140-A1 1,4-Dihydropyridine derivatives Pfizer Limited (GB) 1990-04-25 EP disclosed
EP-0310386-A2 4-Aryl-5-carbamoyl-1,4-dihydropyridines Pfizer Limited (GB) 1989-04-05 EP disclosed