Bromide

Bromide

SCHEMBL2246198

Br.O=c1[nH]ccc2cnccc12

nearest known ligand 0.52

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
▸ PARP1 P09874 3/20 0.52
▸ KDM4C Q9H3R0 3/20 0.49
▸ KDM4A O75164 1/20 0.49
▸ KDM4B O94953 1/20 0.49
▸ KDM5C P41229 1/20 0.49
▸ KDM5B Q9UGL1 1/20 0.49
▸ KDM3A Q9Y4C1 1/20 0.49
▸ GSK3B P49841 2/20 0.42
▸ JAK2 O60674 2/20 0.42
▸ AURKA O14965 1/20 0.42
▸ DAPK3 O43293 1/20 0.42
▸ ROCK2 O75116 1/20 0.42
▸ CHEK2 O96017 1/20 0.42
▸ CDK1 P06493 1/20 0.42
▸ PIM1 P11309 1/20 0.42
▸ FGFR1 P11362 1/20 0.42
▸ PRKACA P17612 1/20 0.42
▸ RPS6KB1 P23443 1/20 0.42
▸ CDK2 P24941 1/20 0.42
▸ MARK3 P27448 1/20 0.42

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
SCHEMBL30692017 0.98 PARP1 (0.53) PARP1KDM4CKDM4AKDM4BKDM5C
SCHEMBL243725 0.98 PARP1 (0.53) PARP1KDM4CKDM4AKDM4BKDM5C
SCHEMBL1159186 0.82 PARP1 (0.53) PARP1KDM4CKDM4AKDM4BKDM5C
SCHEMBL28693642 0.75 CHEK1 (0.49) PARP1KDM4CROCK2PRKACAPRKCD
SCHEMBL1934489 0.74 AURKA (0.46) GSK3BJAK2AURKADAPK3ROCK2
SCHEMBL21224465 0.74 PARP1 (0.52) PARP1KDM4CKDM4AKDM4BKDM5C
Bromide SCHEMBL27922950 0.71 IMPDH2 (0.56) GSK3BJAK2AURKADAPK3ROCK2
Bromide SCHEMBL2722104 0.71 PDE3B (0.48) PIM1MAPTPDE3BPDE3ADAO
SCHEMBL3394071 0.71 PARP1 (0.60) PARP1KDM4CKDM4AKDM4BKDM5C
SCHEMBL13859948 0.70 IMPDH2 (0.50) PARP1KDM4CKDM4AKDM4BKDM5C

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-20110190263-A1 COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY IRM LLC (BM) 2011-08-04 — — US disclosed
EP-2252613-A1 COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY IRM, LLC (BM) 2010-11-24 — — EP disclosed
WO-2009105717-A1 COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY IRM LLC (BM) 2009-08-27 — — 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 (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-20110190263-A1 COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY GPR119, GPR65, GPR39 PARP1 3416/4885KDM4C 3813/4885KDM4A 3612/4885

“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.

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