Bromide

Bromide

SCHEMBL4392734

Br.NC1=NCCN1Cc1ccccc1

nearest known ligand 0.70

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 13)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 2/20 0.53
HTR1D known ✓ P28221 1/20 0.45
HTR1B known ✓ P28222 1/20 0.45
CHRNB2 P17787 2/20 0.60
CHRNA4 P43681 2/20 0.60
CHRNA1 P02708 1/20 0.60
CHRNA3 P32297 1/20 0.60
CHRNA7 P36544 1/20 0.60
GAA P10253 1/20 0.47
GFER P55789 1/20 0.47
TYMP P19971 1/20 0.46
CYP1A2 P05177 1/20 0.45
CYP2D6 P10635 1/20 0.45

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
SCHEMBL10076926 0.98 CHRNB2 (0.62) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
SCHEMBL11064695 0.82 CHRNB2 (0.69) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
Hydrochloric Acid SCHEMBL10795479 0.81 CHRNB2 (0.68) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
Hydrochloric Acid SCHEMBL28478794 0.79 CHRNB2 (0.61) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
SCHEMBL8369049 0.79 CHRNA1 (0.43) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
SCHEMBL24467444 0.78 CHRNA1 (0.52) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
SCHEMBL10480710 0.76 CYP2D6 (0.46) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
SCHEMBL1974393 0.76 HTR1D (0.52) SIGMAR1GAAGFERCYP1A2CYP2D6
Desnitroimidacloprid SCHEMBL29823081 0.76 CHRNB2 (1.00) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7
SCHEMBL4102420 0.75 HTR1D (0.55) CHRNB2CHRNA4CHRNA1CHRNA3CHRNA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1919921-B1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2012-06-27 EP disclosed
US-7494984-B2 Substituted imidazo[1,2-a]pyrimidines as HIV viral DNA integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2009-02-24 US disclosed
EP-1919921-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS Bristol-Myers Squibb Company (US) 2008-05-14 EP disclosed
WO-2007027754-A1 BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-08 WO disclosed
US-20070049606-A1 Bicyclic heterocycles as HIV-integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2007-03-01 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-20070049606-A1 Bicyclic heterocycles as HIV-integrase inhibitors CCNI, APOBEC3C, CDKN1A SIGMAR1 3960/4885HTR1D 2854/4885HTR1B 3012/4885

“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.