Bromide

Bromide

SCHEMBL7138690

Br.CCCN(C)CCc1c(C)[nH]c2ccc(NC(=O)c3ccc(F)cc3)cc12

nearest known ligand 0.80

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
HTR1F known ✓ P30939 4/20 0.80
HTR1A known ✓ P08908 2/20 0.50
HTR1D known ✓ P28221 2/20 0.50
HTR1B known ✓ P28222 2/20 0.50
MAPT P10636 6/20 0.53
HTR2A P28223 1/20 0.50
HTR2C P28335 1/20 0.50
HTR7 P34969 1/20 0.50
HTR2B P41595 1/20 0.50
HTR6 P50406 1/20 0.50
HTR4 Q13639 1/20 0.50
ALDH1A1 P00352 3/20 0.46
HPGD P15428 1/20 0.46
NPSR1 Q6W5P4 2/20 0.45
LMNA P02545 1/20 0.45
KMT2A Q03164 3/20 0.43
RAB9A P51151 3/20 0.43
NPC1 O15118 2/20 0.43
MEN1 O00255 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42

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
SCHEMBL8598857 0.99 HTR1F (0.81) HTR1FMAPTHTR1AHTR1DHTR1B
SCHEMBL7144771 0.92 HTR1F (0.83) HTR1FMAPTHTR1AHTR1DHTR1B
SCHEMBL7143303 0.89 HTR1F (1.00) HTR1FMAPTHTR1AHTR1DHTR1B
SCHEMBL7140234 0.89 HTR1F (0.77) HTR1FMAPTHTR1AHTR1DHTR1B
Hydrochloric Acid SCHEMBL7138726 0.88 HTR1F (0.98) HTR1FMAPTHTR1AHTR1DHTR1B
Hydrochloric Acid SCHEMBL7140335 0.88 HTR1F (0.76) HTR1FMAPTHTR1AHTR1DHTR1B
SCHEMBL8196218 0.87 HTR1F (0.75) HTR1FMAPTHTR1AHTR1DHTR1B
SCHEMBL8569631 0.85 HTR1F (0.71) HTR1FMAPTHTR1AHTR1DHTR1B
SCHEMBL7141203 0.84 HTR1F (0.73) HTR1FMAPTHTR1AHTR1DHTR1B
Malonic Acid SCHEMBL8215354 0.84 HTR1F (0.70) HTR1FMAPTHTR1AHTR1DHTR1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0768301-B1 N-(2-substituted-3-(2-aminoethyl)-1H-indol-5-yl)-amides as new 5-HT1F agonists LILLY CO ELI (US) 2003-04-02 EP disclosed
US-6380201-B1 Methods of treating or ameliorating the symptoms of common cold or allergic rhinitis with serotonin 5-HT1F agonists ELI LILLY AND COMPANY 2002-04-30 US disclosed
US-6126932-A INSOLUBLE POLYMER BEARING PENDANT SIDE CHAINS, SAID SIDE CHAINS EACH TERMINATING WITH THE 1-(3-(1-PYRROLIDINYL)-PROPYL)-3-ETHYLCARBODIIMIDE MOIETY. ELI LILLY AND COMPANY (US) 2000-10-03 US disclosed
EP-0994109-A2 1-(3-(1-Pyrrolidinyl)propyl)-3-ethylcarbodiimide and a solid phase coupling agent ELI LILLY AND COMPANY (US) 2000-04-19 EP disclosed
US-5998630-A A 1-(3-(1-PYRROLIDINYL)PROPY)-3-ETHYLCARBODIIMIDE ELI LILLY AND COMPANY (US) 1999-12-07 US disclosed
US-5962473-A Methods of treating or ameliorating the symptoms of common cold or allergic rhinitis with serotonin 5-HT1F ELI LILLY AND COMPANY (US) 1999-10-05 US disclosed
US-5942536-A USEFUL FOR TREATING MIGRAINE ELI LILLY AND COMPANY (US) 1999-08-24 US disclosed
EP-0824917-A2 Use of a serotonin 5-HTlf agonist in the manufacture of a medicament for treating or ameliorating the symptoms of common cold or allergic rhinitis ELI LILLY AND COMPANY (US) 1998-02-25 EP disclosed
WO-1997013512-A1 N-[2-SUBSTITUTED-3-(2-AMINOETHYL)-1H-INDOL-5-YL]-AMIDES: NEW 5-HT1F AGONISTS ELI LILLY AND COMPANY (US) 1997-04-17 WO disclosed
EP-0768301-A1 N-(2-substituted-3-(2-aminoethyl)-1H-indol-5-yl)-amides as new 5-HT1F agonists ELI LILLY AND COMPANY (US) 1997-04-16 EP disclosed