Bromide

Bromide

SCHEMBL6830776

Br.CCCCCCCCCCCCCCCCC(CCCN(C)C)=C(C)C(N)=O

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

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
DNM1 Q05193 6/20 0.47
FAAH O00519 3/20 0.39
PAOX Q6QHF9 1/20 0.39
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
TP53 P04637 1/20 0.39
CYP1A2 P05177 1/20 0.39
CYP3A4 P08684 1/20 0.39
CYP2C19 P33261 1/20 0.39
SOAT1 P35610 1/20 0.39
THRB P10828 1/20 0.39
FNTA P49354 1/20 0.39
FNTB P49356 1/20 0.39
PGGT1B P53609 1/20 0.39
CES2 O00748 3/20 0.38
CES1 P23141 3/20 0.38
PPARG P37231 3/20 0.37
PPARD Q03181 3/20 0.37
PPARA Q07869 3/20 0.37
TSHR P16473 2/20 0.37

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
SCHEMBL6829879 0.98 DNM1 (0.49) DNM1FAAHPAOXMEN1KMT2A
SCHEMBL16913010 0.98 DNM1 (0.49) DNM1FAAHPAOXMEN1KMT2A
Hydrochloric Acid SCHEMBL30596838 0.95 DNM1 (0.46) DNM1FAAHPAOXMEN1KMT2A
SCHEMBL27647689 0.86 CES2 (0.50) FAAHMEN1KMT2ATP53CYP1A2
SCHEMBL3467535 0.86 CES2 (0.50) FAAHMEN1KMT2ATP53CYP1A2
SCHEMBL4085870 0.86 CES2 (0.50) FAAHMEN1KMT2ATP53CYP1A2
SCHEMBL27988309 0.86 CES2 (0.50) FAAHMEN1KMT2ATP53CYP1A2
SCHEMBL3466717 0.86 CES2 (0.50) FAAHMEN1KMT2ATP53CYP1A2
SCHEMBL250174 0.86 CES2 (0.50) FAAHMEN1KMT2ATP53CYP1A2
SCHEMBL10592271 0.84 CES2 (0.48) FAAHMEN1KMT2ATP53CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6822061-B2 FOR USE AS FLUID LOSS CONTROL HALLIBURTON ENERGY SERVICES, INC. 2004-11-23 US claimed
US-6743288-B2 FLUID LOSS CONTROL AGENT ACRYLIC TERPOLYMERS HALLIBURTON ENERGY SERVICES, INC. 2004-06-01 US claimed
US-20030096945-A1 Well cement additives, compositions and methods EOFF LARRY S (US) 2003-05-22 US claimed
US-20030094122-A1 Well cement additives, compositions and methods EOFF LARRY S (US) 2003-05-22 US claimed
US-6822061-B2 FOR USE AS FLUID LOSS CONTROL HALLIBURTON ENERGY SERVICES, INC. 2004-11-23 US disclosed
US-6743288-B2 FLUID LOSS CONTROL AGENT ACRYLIC TERPOLYMERS HALLIBURTON ENERGY SERVICES, INC. 2004-06-01 US disclosed
US-20030096945-A1 Well cement additives, compositions and methods EOFF LARRY S (US) 2003-05-22 US disclosed
US-20030094122-A1 Well cement additives, compositions and methods EOFF LARRY S (US) 2003-05-22 US disclosed
US-6497283-B1 CEMENTING USING SLURRY OF WATER, HYDRAULIC CEMENT AND FLUID LOSS CONTROL TERPOLYMER COMPRISING A VINYLSULFONIC ACID, 2-ALLYLOXY-2-HYDROXY-1-PROPANESULFONIC ACID OR 2-ACRYLAMIDO-2-METHYLPROPANESULFONIC ACID MONOMER HALLIBURTON ENERGY SERVICES, INC. 2002-12-24 US disclosed