Bromide

Bromide

SCHEMBL303149

Br.Oc1ccc2c(c1)NCCO2

nearest known ligand 0.61

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
ALDH1A1 P00352 3/20 0.61
MAPT P10636 3/20 0.61
GAA P10253 2/20 0.61
HSD17B10 Q99714 2/20 0.61
PDE3B Q13370 2/20 0.44
PDE3A Q14432 2/20 0.44
DRD2 P14416 2/20 0.43
DRD4 P21917 1/20 0.43
PRKCI P41743 1/20 0.43
CYP3A4 P08684 1/20 0.42
BRD4 O60885 1/20 0.41
FABP6 P51161 1/20 0.39
TRPV1 Q8NER1 1/20 0.39
MAOA P21397 1/20 0.39
MAOB P27338 1/20 0.39
KDM4E B2RXH2 2/20 0.38
GLA P06280 2/20 0.38
HPGD P15428 2/20 0.38
DRD3 P35462 1/20 0.38
CASP1 P29466 1/20 0.38

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 SCHEMBL31327838 1.00 ALDH1A1 (0.61) ALDH1A1MAPTGAAHSD17B10PDE3B
SCHEMBL33867 0.98 ALDH1A1 (0.62) ALDH1A1MAPTGAAHSD17B10PDE3B
SCHEMBL29355887 0.98 ALDH1A1 (0.62) ALDH1A1MAPTGAAHSD17B10PDE3B
SCHEMBL9796104 0.96 ALDH1A1 (0.61) ALDH1A1MAPTGAAHSD17B10PDE3B
Hydrochloric Acid SCHEMBL31200757 0.96 ALDH1A1 (0.61) ALDH1A1MAPTGAAHSD17B10PDE3B
Hydrochloric Acid SCHEMBL31327837 0.96 ALDH1A1 (0.61) ALDH1A1MAPTGAAHSD17B10PDE3B
Sulfuric Acid SCHEMBL31327839 0.90 ALDH1A1 (0.54) ALDH1A1MAPTGAAHSD17B10PDE3B
SCHEMBL27505856 0.84 GAA (0.56) ALDH1A1MAPTGAAHSD17B10PDE3B
SCHEMBL2746377 0.83 ALDH1A1 (0.49) ALDH1A1MAPTGAAHSD17B10PDE3B
SCHEMBL8496939 0.82 ALDH1A1 (0.50) ALDH1A1MAPTGAAHSD17B10PDE3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4739272-A1 OXIDATIVE HAIR COLOURING COMPOSITION Wella Germany GmbH (DE) 2026-05-13 EP disclosed
WO-2025008339-A1 OXIDATIVE HAIR COLOURING COMPOSITION WELLA GERMANY GMBH (DE) 2025-01-09 WO disclosed
US-8242116-B2 Fused thiazole derivatives as kinase inhibitors UCB PHARMA S.A. (BE) 2012-08-14 US disclosed
US-8093238-B2 Fused thiazole derivatives as kinase inhibitors UCB PHARMA S.A. (BE) 2012-01-10 US disclosed
EP-2035436-B1 FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS UCB PHARMA SA (BE) 2011-05-25 EP disclosed
US-20100137302-A1 Fused Thiazole Derivatives as Kinase Inhibitors UCB PHARMA S.A. (BE) 2010-06-03 US disclosed
US-20100069361-A1 Fused Thiazole Derivatives as Kinase Inhibitors UCB PHARMA S.A. (BE) 2010-03-18 US disclosed
EP-2076512-A1 FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS UCB Pharma S.A. (BE) 2009-07-08 EP disclosed
WO-2009071895-A1 FUSED THIAZOLE AND THIOPHENE DERIVATIVES AS KINASE INHIBITORS UCB PHARMA S.A. (BE) 2009-06-11 WO disclosed
EP-2035436-A1 FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS UCB Pharma S.A. (BE) 2009-03-18 EP disclosed
WO-2008044022-A1 FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS UCB PHARMA S.A. (BE) 2008-04-17 WO disclosed
WO-2008001076-A1 FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS UCB PHARMA S.A. (BE) 2008-01-03 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 (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-20100069361-A1 Fused Thiazole Derivatives as Kinase Inhibitors JAK1, MTOR, MOK ALDH1A1 1714/4885MAPT 1997/4885GAA 1343/4885
US-20100137302-A1 Fused Thiazole Derivatives as Kinase Inhibitors PI4KA, PDPK1, PIK3CA ALDH1A1 2279/4885MAPT 955/4885GAA 1760/4885

“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.