Bromide

Bromide

SCHEMBL919214

Br.N[C@H](CCc1ccc(O)cc1)C(=O)O

nearest known ligand 0.65

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
HTR1A known ✓ P08908 1/20 0.45
ADRA2A known ✓ P08913 1/20 0.45
SLC6A2 known ✓ P23975 1/20 0.45
HTR3A known ✓ P46098 1/20 0.45
SLC7A5 Q01650 3/20 0.65
GRIK1 P39086 2/20 0.53
GRIA1 P42261 1/20 0.53
GRIA2 P42262 1/20 0.53
GRIA3 P42263 1/20 0.53
GRIA4 P48058 1/20 0.53
GRIK2 Q13002 1/20 0.53
GRIK3 Q13003 1/20 0.53
KIF11 P52732 1/20 0.51
GRM8 O00222 1/20 0.49
GRM4 Q14833 1/20 0.49
ANPEP P15144 2/20 0.48
ERAP2 Q6P179 2/20 0.48
ERAP1 Q9NZ08 2/20 0.48
LAP3 P28838 1/20 0.48
ENPEP Q07075 1/20 0.48

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 SCHEMBL29399073 1.00 SLC7A5 (0.65) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL1666620 0.98 SLC7A5 (0.67) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL9394667 0.98 SLC7A5 (0.67) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL1768639 0.98 SLC7A5 (0.67) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL1666513 0.89 SLC7A5 (0.56) SLC7A5GRIK1GRIA1GRIA2GRIA3
Homophenylalanine SCHEMBL1318350 0.87 SLC7A5 (0.73) SLC7A5GRIK1GRIA2KIF11ANPEP
SCHEMBL22851020 0.85 SLC7A5 (0.51) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL25356342 0.83 GRIK1 (0.54) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL3629108 0.83 GRIK1 (0.54) SLC7A5GRIK1GRIA1GRIA2GRIA3
SCHEMBL6377896 0.83 GRIK1 (0.54) SLC7A5GRIK1GRIA1GRIA2GRIA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7871998-B2 Diphenylazetidinone derivatives possessing cholesterol absorption inhibitory activity ASTRAZENECA AB (SE) 2011-01-18 US disclosed
US-20100099657-A2 Diphenylazetidinone Derivatives Possessing Cholesterol Absorption Inhibitory Activity ASTRAZENECA AB (SE) 2010-04-22 US disclosed
US-20080064676-A1 Diphenylazetidinone Derivatives Possessing Cholesterol Absorption Inhibitory Activity ASTRAZENECA AB (SE) 2008-03-13 US disclosed
EP-0662481-B1 Spiro piperidines and homologs promote release of growth hormone MERCK & CO INC (US) 1999-03-24 EP disclosed
US-5578593-A RELEASING GROWTH HORMONES FOR ANIMALS MERCK & CO., INC. (US) 1996-11-26 US disclosed
EP-0662481-A1 Spiro piperidines and homologs promote release of growth hormone MERCK & CO. INC. (US) 1995-07-12 EP disclosed
WO-1994019367-A1 SPIRO PIPERIDINES AND HOMOLOGS PROMOTE RELEASE OF GROWTH HORMONE MERCK & CO., INC. (US) 1994-09-01 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100099657-A2 Diphenylazetidinone Derivatives Possessing Cholesterol Absorption Inhibitory Activity CYP46A1, CYP51A1, DHCR7 HTR1A 3112/4885ADRA2A 1293/4885SLC6A2 1057/4885
US-20080064676-A1 Diphenylazetidinone Derivatives Possessing Cholesterol Absorption Inhibitory Activity CYP46A1, CYP51A1, DHCR7 HTR1A 3112/4885ADRA2A 1293/4885SLC6A2 1057/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.