Bromide

Bromide

SCHEMBL2192386

Br.COc1ccc(Cc2nccn2C)cc1OC

nearest known ligand 0.54

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
ACHE known ✓ P22303 1/20 0.48
CA2 P00918 1/20 0.54
ALDH1A1 P00352 5/20 0.48
POLB P06746 5/20 0.48
GAA P10253 2/20 0.48
MPI P34949 1/20 0.48
APOBEC3G Q9HC16 1/20 0.48
LMNA P02545 3/20 0.48
MAPK1 P28482 3/20 0.48
USP2 O75604 2/20 0.48
CYP3A4 P08684 2/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
HIF1A Q16665 2/20 0.48
PDE10A Q9Y233 2/20 0.48
PDE2A O00408 1/20 0.48
ABCC4 O15439 1/20 0.48
PDE5A O76074 1/20 0.48
ABCB11 O95342 1/20 0.48
CYP1A2 P05177 1/20 0.48
CYP2D6 P10635 1/20 0.48

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
SCHEMBL1008065 0.98 CA2 (0.56) CA2ALDH1A1POLBGAAMPI
SCHEMBL16879029 0.86 MAPK1 (0.47) CA2ALDH1A1APOBEC3GLMNAMAPK1
SCHEMBL29002529 0.75 TSHR (0.46) ALDH1A1GAAMAPK1SMN1; SMN2TSHR
SCHEMBL4856194 0.74 TSHR (0.51) ALDH1A1MAPK1SMN1; SMN2TSHRRAB9A
SCHEMBL2095593 0.73 CA2 (1.00) CA2ALDH1A1POLBGAALMNA
SCHEMBL12409075 0.72 NPC1 (0.50) ALDH1A1POLBMAPK1USP2CYP2C9
SCHEMBL5601356 0.72 CHRNB2 (0.39) ALDH1A1POLBLMNAMAPK1CYP3A4
SCHEMBL3924901 0.71 CA2 (0.66) CA2ALDH1A1POLBLMNAMAPK1
SCHEMBL20204951 0.71 CYP11B1 (0.45) ALDH1A1POLBMAPTNPSR1MEN1
SCHEMBL20871500 0.71 CA2 (0.59) CA2ALDH1A1POLBSMN1; SMN2KDM4E

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-8980875-B2 Platinum-N-heterocyclic carbene derivatives, preparation thereof and therapeutic use thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2015-03-17 US disclosed
US-20130338128-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2013-12-19 US disclosed
US-8481522-B2 Platinum-N-heterocyclic carbene derivatives, preparation thereof and therapeutic use thereof SANOFI (FR) 2013-07-09 US disclosed
US-20110172199-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SANOFI-AVENTIS (FR) 2011-07-14 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 (2 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-20130338128-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SCO2, C3AR1, IDH1 ACHE 3731/4885CA2 554/4885ALDH1A1 1989/4885
US-20110172199-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SCO2, C3AR1, IDH1 ACHE 3731/4885CA2 554/4885ALDH1A1 1989/4885

“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.