Bromide

Bromide

SCHEMBL6049682

Br.N[C@@H](CCCCOc1ccc(Cc2ccccc2)cc1)C(=O)O

nearest known ligand 0.56

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 6)

geneUniProtsupporting neighboursconfidence
ITGB3 P05106 1/20 0.56
ITGA2B P08514 1/20 0.56
LTA4H P09960 16/20 0.55
L3MBTL1 Q9Y468 1/20 0.51
FFAR1 O14842 1/20 0.49
SLC5A1 P13866 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 SCHEMBL6049677 1.00 ITGB3 (0.56) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Bromide SCHEMBL6049795 0.99 ITGB3 (0.58) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Bromide SCHEMBL6049794 0.99 ITGB3 (0.58) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Bromide SCHEMBL6049776 0.99 ITGB3 (0.58) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Bromide SCHEMBL6049780 0.99 ITGB3 (0.58) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
SCHEMBL4105743 0.99 ITGB3 (0.57) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
SCHEMBL6552724 0.97 ITGB3 (0.59) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Hydrochloric Acid SCHEMBL6552412 0.96 ITGB3 (0.58) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Hydrochloric Acid SCHEMBL6550947 0.96 ITGB3 (0.58) ITGB3ITGA2BLTA4HL3MBTL1FFAR1
Bromide SCHEMBL6049771 0.96 LTA4H (0.56) ITGB3ITGA2BLTA4HL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6878723-B1 Carbocyclic and/or heterocyclic amino carboxylic acids, e.g., 2-aminomethyl-6-(p-benzylphenoxy)hexanoic acid; leukotriene A4 hydrolase; treating arthritis and psoriasis; hematoprotective and antimitotic agents INSTITUT NATIONAL DE LA SANTE ET DE LA RESCHERCHE MEDICALE (INSERM) (FR) 2005-04-12 US claimed
US-7094773-B2 LTA4 hydrolase inhibitors Institut National de la Santa et de la rescherche Medicale Bioprojet (FR) 2006-08-22 US disclosed
US-6878723-B1 Carbocyclic and/or heterocyclic amino carboxylic acids, e.g., 2-aminomethyl-6-(p-benzylphenoxy)hexanoic acid; leukotriene A4 hydrolase; treating arthritis and psoriasis; hematoprotective and antimitotic agents INSTITUT NATIONAL DE LA SANTE ET DE LA RESCHERCHE MEDICALE (INSERM) (FR) 2005-04-12 US disclosed
US-20050027013-A1 LTA4 hydrolase inhibitors DANVY DENIS (FR) 2005-02-03 US 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 (1 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-20050027013-A1 LTA4 hydrolase inhibitors LTA4H, LTC4S, LTB4R ITGB3 2057/4885ITGA2B 2512/4885LTA4H 1/4885

“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.