Bromide

Bromide

SCHEMBL6522977

Br.OCCN1CCc2ccccc2C1

nearest known ligand 0.68

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 19)

geneUniProtsupporting neighboursconfidence
HTR1A known ✓ P08908 5/20 0.56
SLC6A4 known ✓ P31645 1/20 0.55
HDAC3 O15379 2/20 0.58
HDAC1 Q13547 2/20 0.58
HDAC8 Q9BY41 2/20 0.58
NCOR2 Q9Y618 2/20 0.58
KDM4E B2RXH2 2/20 0.57
ALDH1A1 P00352 1/20 0.57
HTR7 P34969 6/20 0.56
DRD3 P35462 5/20 0.56
HTR2A P28223 4/20 0.56
HTR2B P41595 4/20 0.56
DRD2 P14416 3/20 0.55
HRH1 P35367 2/20 0.55
ALOX15 P16050 1/20 0.54
HTR2C P28335 1/20 0.53
HDAC2 Q92769 1/20 0.52
MAOA P21397 1/20 0.52
MAOB P27338 1/20 0.52

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
SCHEMBL30381429 0.98 HDAC3 (0.59) HDAC3HDAC1HDAC8NCOR2KDM4E
SCHEMBL1193409 0.98 HDAC3 (0.59) HDAC3HDAC1HDAC8NCOR2KDM4E
Bromide SCHEMBL6523006 0.89 HTR1A (0.60) HDAC3HDAC1HDAC8NCOR2KDM4E
Acetic Acid SCHEMBL6524206 0.89 DRD2 (0.59) HDAC3HDAC1HDAC8NCOR2KDM4E
SCHEMBL6811660 0.88 SLC18A3 (0.52) HDAC3HDAC1HDAC8NCOR2HTR7
SCHEMBL16380575 0.87 CARM1 (0.52) HDAC3HDAC1HDAC8NCOR2KDM4E
SCHEMBL1828054 0.87 HTR1A (0.61) HDAC3HDAC1HDAC8NCOR2KDM4E
SCHEMBL30305062 0.87 HTR1A (0.61) HDAC3HDAC1HDAC8NCOR2KDM4E
Hydrochloric Acid SCHEMBL22527658 0.86 HTR1A (0.60) HDAC3HDAC1HDAC8NCOR2HTR7
Hydrochloric Acid SCHEMBL30541930 0.86 HTR1A (0.60) HDAC3HDAC1HDAC8NCOR2HTR7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2274056-B1 BLEACHING AGENT COMPRISING CATIONIC 3,4-DIHYDROISOCHINOLINIUM DERIVATIVES, SPECIFIC ALKANOLAMINES AND HYDROGEN PEROXYDE HENKEL AG & CO KGAA (DE) 2012-10-03 EP claimed
US-20110056508-A1 BLEACHING AGENT COMPRISING CATIONIC 3,4-DIHYDROISOQUINOLINE DERIVATIVES, SPECIAL ALKANOL AMINES AND HYDROGEN PEROXIDE GROSS WIBKE 2011-03-10 US claimed
US-20110056508-A1 BLEACHING AGENT COMPRISING CATIONIC 3,4-DIHYDROISOQUINOLINE DERIVATIVES, SPECIAL ALKANOL AMINES AND HYDROGEN PEROXIDE GROSS WIBKE 2011-03-10 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-20110056508-A1 BLEACHING AGENT COMPRISING CATIONIC 3,4-DIHYDROISOQUINOLINE DERIVATIVES, SPECIAL ALKANOL AMINES AND HYDROGEN PEROXIDE KRT18, H1-3, H1-2 HTR1A 715/4885SLC6A4 2770/4885HDAC3 95/4885

“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.