Bromide

Bromide

SCHEMBL1940375

Br.c1cc(-c2cc(C3CCNCC3)n[nH]2)ccn1

nearest known ligand 0.58

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
MKNK1 Q9BUB5 4/20 0.58
MKNK2 Q9HBH9 4/20 0.58
CDC7 O00311 1/20 0.47
MAPK11 Q15759 2/20 0.44
MAPK14 Q16539 2/20 0.44
MAPK13 O15264 1/20 0.39
RAF1 P04049 1/20 0.39
MAPK9 P45984 1/20 0.39
MAPK12 P53778 1/20 0.39
TLR9 Q9NR96 2/20 0.38
TLR8 Q9NR97 2/20 0.38
TLR7 Q9NYK1 2/20 0.38
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
CHEK1 O14757 1/20 0.37
RPS6KA3 P51812 1/20 0.36
HRH4 Q9H3N8 1/20 0.36
PKN2 Q16513 1/20 0.36
BRAF P15056 1/20 0.36
PDPK1 O15530 1/20 0.36

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
SCHEMBL6032677 0.98 MKNK1 (0.60) MKNK1MKNK2CDC7MAPK11MAPK14
SCHEMBL27696604 0.84 POLB (0.51) MKNK1MKNK2MEN1KMT2APOLB
Hydrochloric Acid SCHEMBL3881594 0.83 POLB (0.50) MKNK1MKNK2MEN1KMT2APOLB
SCHEMBL20134937 0.82 SMN1; SMN2 (0.49) MKNK1MKNK2MEN1KMT2ACHEK1
SCHEMBL2755249 0.82 MKNK1 (0.49) MKNK1MKNK2MEN1KMT2APOLB
SCHEMBL31601884 0.81 ALDH1A1 (0.51) MKNK1MKNK2PKN2PIM1
SCHEMBL31601724 0.81 HTR2C (0.53) MKNK1MKNK2MEN1KMT2APOLB
SCHEMBL31601661 0.81 ALDH1A1 (0.51) MKNK1MKNK2PKN2PIM1
SCHEMBL31601739 0.80 TLR7 (0.47) MKNK1MKNK2TLR9TLR8TLR7
SCHEMBL31601793 0.80 MKNK1 (0.45) MKNK1MKNK2CDC7TLR9TLR8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1622616-B1 INHIBITORS OF AKT ACTIVITY MERCK SHARP & DOHME (US) 2011-06-15 EP disclosed
US-7579355-B2 Inhibitors of Akt activity MERCK & CO., INC. (US) 2009-08-25 US disclosed
US-20070043001-A1 Inhibitors of akt activity MERCK SHARP & DOHME CORP. 2007-02-22 US disclosed
CN-1809354-A Inhibitors of Akt activity MERCK & CO INC (US) 2006-07-26 CN disclosed
EP-1622616-A2 INHIBITORS OF AKT ACTIVITY Merck & Co., Inc. (US) 2006-02-08 EP disclosed
WO-2004096131-A2 INHIBITORS OF AKT ACTIVITY MERCK & CO., INC. (US) 2004-11-11 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 (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-20070043001-A1 Inhibitors of akt activity MTMR1, PIK3CA, PLK1 MKNK1 22/4885MKNK2 21/4885CDC7 156/4885

“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.