Bromide

Bromide

SCHEMBL15466254

Br.Clc1ccc2c(c1)CNC(c1ccncc1)c1cccn1-2

nearest known ligand 0.59

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 16)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 2/20 0.59
▸ SMN1; SMN2 Q16637 2/20 0.53
▸ TSHR P16473 2/20 0.53
▸ MAPK1 P28482 2/20 0.53
▸ KMT2A Q03164 12/20 0.49
▸ MEN1 O00255 11/20 0.49
▸ ATM Q13315 3/20 0.49
▸ HSD17B10 Q99714 2/20 0.49
▸ LMNA P02545 2/20 0.49
▸ KDM4E B2RXH2 1/20 0.43
▸ ALDH1A1 P00352 1/20 0.43
▸ HPGD P15428 1/20 0.43
▸ CASP1 P29466 1/20 0.43
▸ CASP7 P55210 1/20 0.43
▸ POLB P06746 1/20 0.40
▸ PTPN1 P18031 1/20 0.39

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
SCHEMBL13726616 0.99 L3MBTL1 (0.60) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
Bromide SCHEMBL15465949 0.91 L3MBTL1 (0.59) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
Bromide SCHEMBL15466167 0.77 L3MBTL1 (0.48) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL13726427 0.76 L3MBTL1 (0.49) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL13726870 0.76 L3MBTL1 (0.49) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL9289890 0.72 L3MBTL1 (0.57) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL15317613 0.71 TSHR (0.97) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL8534290 0.70 L3MBTL1 (0.55) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL9286188 0.70 L3MBTL1 (0.55) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A
SCHEMBL18215112 0.69 TSHR (0.71) L3MBTL1SMN1; SMN2TSHRMAPK1KMT2A

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-9493468-B2 Antifungal 5,6-dihydro-4H-pyrrolo[1,2-a][1,4]benzo-diazepines and 6H-pyrrolo[1,2-a][1,4]benzodiazepines substituted with heterocyclic derivatives JANSSEN PHARMACEUTICA NV (BE) 2016-11-15 — — US disclosed
US-20140045827-A1 NOVEL ANTIFUNGAL 5,6-DIHYDRO-4H-PYRROLO[1,2-a][1,4]BENZO-DIAZEPINES AND 6H-PYRROLO[1,2-a][1,4]BENZODIAZEPINES SUBSTITUTED WITH HETEROCYCLIC DERIVATIVES JANSSEN PHARMACEUTICA NV (BE) 2014-02-13 — — 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-20140045827-A1 NOVEL ANTIFUNGAL 5,6-DIHYDRO-4H-PYRROLO[1,2-a][1,4]BENZO-DIAZEPINES AND 6H-PYRROLO[1,2-a][1,4]BENZODIAZEPINES SUBSTITUTED WITH HETEROCYCLIC DERIVATIVES GABBR1, HRH4, CYP1B1 L3MBTL1 4609/4885SMN1; SMN2 4689/4885TSHR 2263/4885

“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.

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