Bromide

Bromide

SCHEMBL6428082

Br.CCC1SC(NC2CC3CCC2C3)=NC1=O

nearest known ligand 0.36

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 19)

geneUniProtsupporting neighboursconfidence
JAK2 O60674 2/20 0.36
JAK1 P23458 2/20 0.36
TAS1R3 Q7RTX0 1/20 0.33
TAS1R1 Q7RTX1 1/20 0.33
TAS1R2 Q8TE23 1/20 0.33
P2RX7 Q99572 1/20 0.33
GABBR2 O75899 3/20 0.33
GABBR1 Q9UBS5 3/20 0.33
MEN1 O00255 1/20 0.33
ALDH1A1 P00352 1/20 0.33
KMT2A Q03164 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
CNR2 P34972 1/20 0.33
EPHX2 P34913 2/20 0.33
PDGFRB P09619 3/20 0.32
PDGFRA P16234 3/20 0.32
PANK3 Q9H999 1/20 0.32
BRS3 P32247 2/20 0.32
JAK3 P52333 1/20 0.32

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
SCHEMBL1382870 0.99 JAK2 (0.36) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL10285219 0.88 JAK2 (0.35) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1605212 0.84 JAK2 (0.36) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1605209 0.84 JAK2 (0.36) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1605427 0.83 JAK2 (0.35) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1605303 0.83 JAK2 (0.35) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1605306 0.83 JAK2 (0.35) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1604882 0.82 EPHX2 (0.36) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL10284770 0.81 EPHX2 (0.35) JAK2JAK1TAS1R3TAS1R1TAS1R2
SCHEMBL1605816 0.81 EPHX1 (0.40) JAK2JAK1P2RX7GABBR2GABBR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050239853-A1 New compounds BIOVITRUM AB (SE) 2005-10-27 US claimed
WO-2005075471-A2 THIAZOL-COMPOUNDS AS 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITORS BIOVITRUM AB (SE) 2005-08-18 WO claimed
US-20050239853-A1 New compounds BIOVITRUM AB (SE) 2005-10-27 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 (1 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-20050239853-A1 New compounds HSD11B1, CYP11B1, HSD3B1 JAK2 4247/4885JAK1 3780/4885TAS1R3 4345/4885

“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.