Bromide

Bromide

SCHEMBL6797578

Br.CN1C(=O)C(N)N=C(c2ccc(C(F)(F)F)cc2)c2ccccc21

nearest known ligand 0.73

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
PSEN1 known ✓ P49768 8/20 0.49
PSEN2 known ✓ P49810 8/20 0.49
APH1B known ✓ Q8WW43 8/20 0.49
NCSTN known ✓ Q92542 8/20 0.49
APH1A known ✓ Q96BI3 8/20 0.49
PSENEN known ✓ Q9NZ42 8/20 0.49
GABRP O00591 1/20 0.73
GABRD O14764 1/20 0.73
GABRA1 P14867 1/20 0.73
GABRB1 P18505 1/20 0.73
GABRG2 P18507 1/20 0.73
GABRB3 P28472 1/20 0.73
GABRA5 P31644 1/20 0.73
GABRA3 P34903 1/20 0.73
GABRA2 P47869 1/20 0.73
GABRB2 P47870 1/20 0.73
GABRA4 P48169 1/20 0.73
GABRE P78334 1/20 0.73
GABRA6 Q16445 1/20 0.73
GABRG1 Q8N1C3 1/20 0.73

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 SCHEMBL6797581 1.00 GABRP (0.73) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL4115829 0.99 GABRP (0.74) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL3287888 0.99 GABRP (0.74) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL3289463 0.99 GABRP (0.74) GABRPGABRDGABRA1GABRB1GABRG2
Bromide SCHEMBL6797572 0.96 GABRP (0.71) GABRPGABRDGABRA1GABRB1GABRG2
Bromide SCHEMBL3486697 0.87 GABRP (0.68) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL3487036 0.86 GABRP (0.70) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL3287133 0.85 GABRP (0.80) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL2923672 0.85 GABRA1 (1.00) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL1835654 0.85 GABRA1 (1.00) GABRPGABRDGABRA1GABRB1GABRG2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6713476-B2 SUBSTITUTED LACTAM; GAMMA-SECRETASE INHIBITOR; DECREASES PRODUCTION OF BETA-AMYLOID; TREATMENT FOR ALTZHEIMER'S AND DOWN'S SYNDROME DUPONT PHARMACEUTICALS COMPANY 2004-03-30 US disclosed
US-20020061874-A1 Substituted cycloalkyls as inhibitors of a beta protein production BRISTOL-MYERS SQUIBB PHARMA COMPANY 2002-05-23 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-20020061874-A1 Substituted cycloalkyls as inhibitors of a beta protein production APP, BACE1, APH1A PSEN1 6/4885PSEN2 8/4885APH1B 4/4885

“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.