Bromide

Bromide

SCHEMBL3889460

Br.Cc1cccc(C(=O)C(Br)c2cc(C)nc(C)c2)c1

nearest known ligand 0.46

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
SLC6A2 known ✓ P23975 2/20 0.43
SLC6A3 known ✓ Q01959 2/20 0.43
SLC6A4 known ✓ P31645 1/20 0.39
ENPP3 O14638 2/20 0.44
ALPL P05186 2/20 0.44
XIAP P98170 2/20 0.44
PARP1 P09874 1/20 0.44
GRM5 P41594 1/20 0.43
CHRNA1 P02708 1/20 0.43
CHRNG P07510 1/20 0.43
CHRNB1 P11230 1/20 0.43
CHRNB2 P17787 1/20 0.43
CHRNB4 P30926 1/20 0.43
CHRNA3 P32297 1/20 0.43
CHRNA4 P43681 1/20 0.43
CHRND Q07001 1/20 0.43
GBA1 P04062 1/20 0.42
ELANE P08246 3/20 0.42
HDAC8 Q9BY41 1/20 0.41
HDAC6 Q9UBN7 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
Bromide SCHEMBL3888884 0.85 PARP1 (0.41) ENPP3ALPLXIAPPARP1GRM5
Bromide SCHEMBL3894636 0.84 TPMT (0.38) LMNARAB9AHPGDSMN1; SMN2MAPT
SCHEMBL6602649 0.83 TPMT (0.39) ENPP3ALPLXIAPLMNARAB9A
SCHEMBL17762880 0.83 PARP1 (0.50) PARP1SLC6A2SLC6A3CHRNA1CHRNG
Bromide SCHEMBL6283062 0.82 NT5E (0.51) PARP1GRM5SLC6A2SLC6A3CHRNA1
SCHEMBL7143390 0.81 NT5E (0.52) PARP1GRM5SLC6A2SLC6A3CHRNA1
Bromide SCHEMBL6284648 0.79 NPC1 (0.50) GRM5ELANELMNARAB9AMAPT
SCHEMBL7148265 0.77 NPC1 (0.51) PARP1GRM5ELANELMNARAB9A
Bromide SCHEMBL3888871 0.77 PARP1 (0.39) PARP1SLC6A2SLC6A3CHRNA1CHRNG
Bromide SCHEMBL3889498 0.77 PARP1 (0.42) PARP1SLC6A2SLC6A3CHRNA1CHRNG

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 8 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-1205478-A1 p38MAP KINASE INHIBITORS Takeda Chemical Industries, Ltd. (JP) 2002-05-15 EP 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 SLC6A2 4327/4885SLC6A3 4560/4885SLC6A4 4742/4885
US-20040053973-A1 Substituted 1,3-thiazole compounds, their production and use MAPK1, MAP4K2, MAPK4 SLC6A2 3311/4885SLC6A3 1948/4885SLC6A4 1822/4885
US-20040097555-A1 Concomitant drugs TNF, CHUK, CNKSR1 SLC6A2 2202/4885SLC6A3 3378/4885SLC6A4 2106/4885

“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.