Bromide

Bromide

SCHEMBL3888884

Br.Cc1cccc(C(=O)C(Br)c2ccnc(C)c2)c1

nearest known ligand 0.42

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
PSEN1 known ✓ P49768 4/20 0.40
PSEN2 known ✓ P49810 4/20 0.40
APH1B known ✓ Q8WW43 4/20 0.40
NCSTN known ✓ Q92542 4/20 0.40
APH1A known ✓ Q96BI3 4/20 0.40
PSENEN known ✓ Q9NZ42 4/20 0.40
SLC6A2 known ✓ P23975 1/20 0.40
SLC6A3 known ✓ Q01959 1/20 0.40
PARP1 P09874 1/20 0.41
CHRNA1 P02708 1/20 0.40
CHRNG P07510 1/20 0.40
CHRNB1 P11230 1/20 0.40
CHRNB2 P17787 1/20 0.40
CHRNB4 P30926 1/20 0.40
CHRNA3 P32297 1/20 0.40
CHRNA4 P43681 1/20 0.40
CHRND Q07001 1/20 0.40
ENPP3 O14638 1/20 0.39
ALPL P05186 1/20 0.39
XIAP P98170 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
Bromide SCHEMBL3888186 0.87 PSEN1 (0.40) PSEN1PSEN2APH1BNCSTNAPH1A
Bromide SCHEMBL3888871 0.87 PARP1 (0.39) PARP1CHRNA1CHRNGCHRNB1CHRNB2
Bromide SCHEMBL3889498 0.87 PARP1 (0.42) PARP1CHRNA1CHRNGCHRNB1CHRNB2
SCHEMBL5114755 0.85 PARP1 (0.40) PARP1CHRNA1CHRNGCHRNB1CHRNB2
SCHEMBL6505647 0.85 PARP1 (0.43) PARP1CHRNA1CHRNGCHRNB1CHRNB2
Bromide SCHEMBL3889460 0.85 ENPP3 (0.44) PARP1CHRNA1CHRNGCHRNB1CHRNB2
Bromide SCHEMBL6283062 0.85 NT5E (0.51) PARP1CHRNA1CHRNGCHRNB1CHRNB2
SCHEMBL7143390 0.83 NT5E (0.52) PARP1CHRNA1CHRNGCHRNB1CHRNB2
SCHEMBL17762880 0.82 PARP1 (0.50) PARP1CHRNA1CHRNGCHRNB1CHRNB2
Bromide SCHEMBL5200336 0.81 NPC1 (0.57) NPC1RAB9AKCNK3KCNK9GRM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7495018-B2 Substituted 1,3-thiazole compounds, their production and use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-02-24 US disclosed
US-6962933-B1 Method for inhibiting p38 MAP kinase or TNF-α production using a 1,3-thiazole TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2005-11-08 US disclosed
US-20050080113-A1 Medicinal compositions TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2005-04-14 US disclosed
US-20040097555-A1 Concomitant drugs TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2004-05-20 US disclosed
EP-1402900-A1 MEDICINAL COMPOSITIONS Takeda Chemical Industries, Ltd. (JP) 2004-03-31 EP disclosed
US-20040053973-A1 Substituted 1,3-thiazole compounds, their production and use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2004-03-18 US disclosed
EP-1354603-A1 CONCOMITANT DRUGS Takeda Chemical Industries, Ltd. (JP) 2003-10-22 EP disclosed
EP-1268474-A2 SUBSTITUTED 1,3-THIAZOLE COMPOUNDS, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 2003-01-02 EP disclosed
EP-1205478-A1 p38MAP KINASE INHIBITORS Takeda Chemical Industries, Ltd. (JP) 2002-05-15 EP disclosed
WO-2001074811-A2 SUBSTITUTED 1,3-THIAZOLE COMPOUNDS, THEIR PRODUCTION AND USE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-10-11 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 (3 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-20050080113-A1 Medicinal compositions TNF, TRAF6, MMP8 PSEN1 3987/4885PSEN2 4121/4885APH1B 2830/4885
US-20040053973-A1 Substituted 1,3-thiazole compounds, their production and use MAPK1, MAP4K2, MAPK4 PSEN1 3982/4885PSEN2 3444/4885APH1B 4707/4885
US-20040097555-A1 Concomitant drugs TNF, CHUK, CNKSR1 PSEN1 3612/4885PSEN2 3079/4885APH1B 3839/4885

“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.