Bromide

Bromide

SCHEMBL5259259

COc1ccc(C(=O)C[n+]2cccc3ccccc32)cc1.[Br-]

nearest known ligand 0.73

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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
KMT2A Q03164 10/20 0.73
MEN1 O00255 7/20 0.73
KDM4E B2RXH2 7/20 0.73
ALDH1A1 P00352 3/20 0.72
MAPT P10636 3/20 0.64
NPC1 O15118 1/20 0.64
RAB9A P51151 1/20 0.64
HTT P42858 2/20 0.63
MITF O75030 1/20 0.63
TDP1 Q9NUW8 2/20 0.62
LMNA P02545 1/20 0.62
ATM Q13315 1/20 0.60
SMN1; SMN2 Q16637 1/20 0.59
APOBEC3A P31941 2/20 0.58
APOBEC3G Q9HC16 2/20 0.58
USP2 O75604 1/20 0.58
KEAP1 Q14145 1/20 0.58
NFE2L2 Q16236 1/20 0.58
GAA P10253 1/20 0.54
HPGD P15428 1/20 0.51

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 SCHEMBL5257417 0.86 KMT2A (0.73) KMT2AMEN1KDM4EALDH1A1MAPT
Bromide SCHEMBL5257392 0.86 KMT2A (0.67) KMT2AMEN1KDM4EALDH1A1MAPT
Bromide SCHEMBL3624435 0.85 KMT2A (1.00) KMT2AMEN1KDM4EALDH1A1MAPT
Bromide SCHEMBL6228650 0.84 KMT2A (1.00) KMT2AMEN1KDM4EALDH1A1MAPT
SCHEMBL13119940 0.83 KMT2A (0.97) KMT2AMEN1KDM4EALDH1A1MAPT
SCHEMBL30636590 0.82 KMT2A (0.97) KMT2AMEN1KDM4EALDH1A1MAPT
SCHEMBL1128535 0.82 KMT2A (0.97) KMT2AMEN1KDM4EALDH1A1MAPT
Bromide SCHEMBL5258726 0.82 KMT2A (0.78) KMT2AMEN1KDM4EALDH1A1MAPT
Bromide SCHEMBL5257467 0.82 KMT2A (1.00) KMT2AMEN1KDM4EALDH1A1MAPT
Bromide SCHEMBL5258388 0.80 KMT2A (0.71) KMT2AMEN1KDM4EALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1578424-A4 SUBSTITUTED 1-BENZOYL-3-CYANO-PYRROLO 1,2-A| QUINOLINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS CYTOVIA INC (US) 2007-08-08 EP disclosed
US-7135480-B2 Anticarcinogenic agents; colon, lymphoma, lung, prostate and breast cancers CYTOVIA, INC. (US) 2006-11-14 US disclosed
EP-1578424-A2 SUBSTITUTED 1-BENZOYL-3-CYANO-PYRROLO 1,2-A] QUINOLINES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS Cytovia, Inc. (US) 2005-09-28 EP disclosed
US-20050014759-A1 Substituted 1-benzoyl-3-cyano-pyrrolo [1,2-a] quinolines and analogs as activators of caspases and inducers of apoptosis CYTOVIA, INC. 2005-01-20 US disclosed
WO-2004055163-A2 SUBSTITUTED 1-BENZOYL-3-CYANO-PYRROLO[1,2-A]QUINOLINES CYTOVIA, INC. (US) 2004-07-01 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-20050014759-A1 Substituted 1-benzoyl-3-cyano-pyrrolo [1,2-a] quinolines and analogs as activators of caspases and inducers of apoptosis CASP3, CASP7, CASP1 KMT2A 1411/4885MEN1 2503/4885KDM4E 570/4885

“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.