Bromide

Bromide

SCHEMBL6883560

C1=CN(c2ccccn2)CN1c1ccccn1.[Br-].[Br-].[Cu+2]

nearest known ligand 0.44

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
PLD1 Q13393 1/20 0.44
KDM4E B2RXH2 1/20 0.43
CRBN Q96SW2 1/20 0.42
SMN1; SMN2 Q16637 2/20 0.41
GRIN2D O15399 1/20 0.41
GRIN3B O60391 1/20 0.41
GRIN1 Q05586 1/20 0.41
GRIN2A Q12879 1/20 0.41
GRIN2B Q13224 1/20 0.41
GRIN2C Q14957 1/20 0.41
GRIN3A Q8TCU5 1/20 0.41
POLB P06746 1/20 0.39
EP300 Q09472 1/20 0.39
KAT2B Q92831 1/20 0.39
ALDH1A1 P00352 2/20 0.39
HPGD P15428 2/20 0.39
HSD17B10 Q99714 2/20 0.39
PDCD1 Q15116 1/20 0.39
CD274 Q9NZQ7 1/20 0.39
ALOX5 P09917 1/20 0.39

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
SCHEMBL1140766 0.96 PLD1 (0.47) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
Hydrochloric Acid SCHEMBL3827230 0.94 PLD1 (0.46) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL27850842 0.86 KCNH2 (0.42) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL14500987 0.82 SMN1; SMN2 (0.42) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL30657008 0.76 KDM4E (0.40) PLD1KDM4ECRBNSMN1; SMN2POLB
SCHEMBL27735766 0.75 PLD1 (0.35) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL27508033 0.72 PLD1 (0.46) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL6499166 0.71 PLD1 (0.44) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL16637698 0.71 PLD1 (0.44) PLD1KDM4ECRBNSMN1; SMN2GRIN2D
SCHEMBL30565007 0.71 PLD1 (0.44) PLD1KDM4ECRBNSMN1; SMN2GRIN2D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6815562-B2 REACTION OF NITROHALOGENS WITH ANILINES, A BASE AND A CATALYST, HYDROGENATION, BAYER AKTIENGESELLSCHAFT (DE) 2004-11-09 US claimed
US-20040143138-A1 Process for the preparation of nitrodiphenylamines LANXESS DEUTSCHLAND GMBH (DE) 2004-07-22 US claimed
US-6815562-B2 REACTION OF NITROHALOGENS WITH ANILINES, A BASE AND A CATALYST, HYDROGENATION, BAYER AKTIENGESELLSCHAFT (DE) 2004-11-09 US disclosed
US-20040143138-A1 Process for the preparation of nitrodiphenylamines LANXESS DEUTSCHLAND GMBH (DE) 2004-07-22 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-20040143138-A1 Process for the preparation of nitrodiphenylamines HNMT, PNMT, NNMT PLD1 3036/4885KDM4E 1382/4885CRBN 873/4885

“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.