Bromide

Bromide

SCHEMBL6283092

Br.O=C(c1ccccc1Cl)C(Br)c1cccnc1

nearest known ligand 0.49

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 1/20 0.40
SLC6A4 known ✓ P31645 1/20 0.40
SLC6A3 known ✓ Q01959 1/20 0.40
CYP11B2 P19099 1/20 0.49
SMN1; SMN2 Q16637 4/20 0.46
HPGD P15428 2/20 0.43
NPC1 O15118 1/20 0.43
TP53 P04637 1/20 0.43
RAB9A P51151 1/20 0.43
ALDH1A1 P00352 5/20 0.41
HTT P42858 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
LMNA P02545 1/20 0.41
PLAU P00749 1/20 0.41
ELANE P08246 1/20 0.41
VNN1 O95497 1/20 0.41
KCNA5 P22460 2/20 0.40
CFTR P13569 1/20 0.40
GOPC Q9HD26 1/20 0.40
KCNN4 O15554 1/20 0.40

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
SCHEMBL7143404 0.99 CYP11B2 (0.50) CYP11B2SMN1; SMN2HPGDNPC1TP53
Bromide SCHEMBL6280880 0.84 JAK2 (0.49) CYP11B2SMN1; SMN2ALDH1A1LMNAPLAU
Bromide SCHEMBL6284630 0.83 GAA (0.49) SMN1; SMN2ALDH1A1HTTLMNAPLAU
SCHEMBL7148504 0.82 JAK2 (0.50) CYP11B2SMN1; SMN2ALDH1A1LMNAPLAU
SCHEMBL7149098 0.81 GAA (0.50) SMN1; SMN2ALDH1A1HTTLMNAPLAU
Bromide SCHEMBL6282444 0.79 SMN1; SMN2 (0.50) SMN1; SMN2ALDH1A1HTTTDP1LMNA
Bromide SCHEMBL6284312 0.78 CYP19A1 (0.51) CYP11B2SMN1; SMN2NPC1RAB9AALDH1A1
SCHEMBL7140967 0.77 SMN1; SMN2 (0.51) SMN1; SMN2ALDH1A1HTTTDP1LMNA
SCHEMBL7144713 0.77 CYP19A1 (0.53) CYP11B2SMN1; SMN2NPC1RAB9AALDH1A1
SCHEMBL3377623 0.75 CES2 (0.47) SMN1; SMN2HPGDRAB9AALDH1A1PLAU

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
EP-1027050-B1 1,3-THIAZOLES AS ADENOSINE A3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF ALLERGY, ASTHMA AND DIABETES TAKEDA CHEMICAL INDUSTRIES LTD (JP) 2004-01-14 EP 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 (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-20050080113-A1 Medicinal compositions TNF, TRAF6, MMP8 SLC6A2 4327/4885SLC6A4 4742/4885SLC6A3 4560/4885
US-20040097555-A1 Concomitant drugs TNF, CHUK, CNKSR1 SLC6A2 2202/4885SLC6A4 2106/4885SLC6A3 3378/4885

“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.