Bromide

Bromide

SCHEMBL25307759

Br.COc1ccc(-c2cnc(CN)[nH]2)cc1

nearest known ligand 0.63

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
SCN10A Q9Y5Y9 9/20 0.56
SCN2A Q99250 2/20 0.54
CCNB2 O95067 2/20 0.43
CDK1 P06493 2/20 0.43
CCNB1 P14635 2/20 0.43
CCNB3 Q8WWL7 2/20 0.43
GSK3A P49840 1/20 0.43
GSK3B P49841 1/20 0.43
CDK5 Q00535 1/20 0.43
CDK5R1 Q15078 1/20 0.43
DYRK1A Q13627 1/20 0.43
SCN4A P35499 1/20 0.42
SCN5A Q14524 3/20 0.42
SCN1A P35498 1/20 0.41
KCNH2 Q12809 1/20 0.41
SCN9A Q15858 1/20 0.41
SCN8A Q9UQD0 1/20 0.41
RIPK1 Q13546 1/20 0.41
SSTR3 P32745 1/20 0.41
NPC1 O15118 1/20 0.41

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
SCHEMBL25834553 0.98 SCN10A (0.57) SCN10ASCN2ACCNB2CDK1CCNB1
Bromide SCHEMBL25435849 0.81 SCN10A (0.70) SCN10ASCN2ASCN5ASCN1AKCNH2
SCHEMBL25261968 0.80 LOXL2 (0.51) SCN10ASCN5A
SCHEMBL25303086 0.79 SCN10A (0.71) SCN10ASCN2ASCN5ASCN1AKCNH2
SCHEMBL8196299 0.77 LTA4H (0.64) SCN10ASCN2ACCNB2CDK1CCNB1
SCHEMBL20055405 0.77 TRPV1 (0.46) SCN10ACCNB2CDK1CCNB1CCNB3
SCHEMBL2562957 0.76 PDE10A (0.64) SCN2ARAB9A
SCHEMBL12648128 0.76 NLN (0.41) SCN10ASCN2ASCN5ASCN1AKCNH2
SCHEMBL20054552 0.76 NLN (0.43) SCN10ASCN5A
Bromide SCHEMBL16210189 0.75 SCN2A (0.54) SCN10ASCN2ACCNB2CDK1CCNB1

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-20250066370-A1 BICYCLIC TRIAZINE DERIVATIVES FOR THE TREATMENT OF CANCER DEUTSCHES KREBSFORSCH (DE) 2025-02-27 US disclosed
EP-4463458-A1 BICYCLIC TRIAZINE DERIVATIVES FOR THE TREATMENT OF CANCER Deutsches Krebsforschungszentrum (DE) 2024-11-20 EP disclosed
CN-118541372-A Bicyclic triazine derivatives for the treatment of cancer 德国癌症研究中心 2024-08-23 CN disclosed
WO-2023135057-A1 BICYCLIC TRIAZINE DERIVATIVES FOR THE TREATMENT OF CANCER DEUTSCHES KREBSFORSCHUNGSZENTRUM (DE) 2023-07-20 WO 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-20250066370-A1 BICYCLIC TRIAZINE DERIVATIVES FOR THE TREATMENT OF CANCER BRCA1, CCNY, CCND2 SCN10A 4532/4885SCN2A 3859/4885CCNB2 9/4885

“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.