Bromide

Bromide

SCHEMBL6837017

COc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1N.[Br-]

nearest known ligand 0.56

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 18)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.56
SNCA P37840 2/20 0.44
ALDH1A1 P00352 5/20 0.42
CYP3A4 P08684 1/20 0.42
ADRA2B P18089 1/20 0.42
PTGS1 P23219 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
MEN1 O00255 1/20 0.41
MAPT P10636 1/20 0.41
THRB P10828 1/20 0.41
KMT2A Q03164 1/20 0.41
APP P05067 1/20 0.40
LDHA P00338 1/20 0.39
LMNA P02545 1/20 0.38
HTT P42858 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
TRAP1 Q12931 1/20 0.38
IDO1 P14902 1/20 0.38

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 SCHEMBL29880790 0.86 LDHA (0.53) SNCAALDH1A1TDP1MAPTKMT2A
Bromide SCHEMBL4260842 0.86 LDHA (0.53) SNCAALDH1A1TDP1MAPTKMT2A
SCHEMBL30596298 0.84 LDHA (0.54) SNCAALDH1A1TDP1MAPTKMT2A
Hydrochloric Acid SCHEMBL10424163 0.83 LDHA (0.53) SNCAALDH1A1TDP1MAPTKMT2A
Bromide SCHEMBL10721589 0.82 MEN1 (0.47) GAASNCAALDH1A1MEN1MAPT
Bromide SCHEMBL5407745 0.82 KDM1A (0.46) SNCAALDH1A1LDHALMNAHTT
Hydrochloric Acid SCHEMBL3536559 0.80 KDM1A (0.45) SNCAALDH1A1MEN1MAPTKMT2A
Bromide SCHEMBL5440664 0.80 SNCA (0.45) SNCALDHA
Hydrochloric Acid SCHEMBL5417557 0.79 KDM1A (0.46) SNCAALDH1A1LDHALMNAHTT
Bromide SCHEMBL7084184 0.79 SNCA (0.44) SNCACYP3A4KMT2ALDHATRAP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6759555-B2 CONDENSING (3,4,5-TRIMETHOXYBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE WITH 3-NITRO-4-METHOXYBENZALDEHYDE, REDUCING THE NITRO INTERMEDIATE TO FORM 2-METHOXY-5-(2-(3,4,5-TRIMETHOXYPHENYL)-ETHENYL)ANILINE AVENTIS PHARMA S.A. (FR) 2004-07-06 US disclosed
US-20030220404-A1 Process for the preparation of combretastatins AVENTIS PHARMA S.A. (FR) 2003-11-27 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-20030220404-A1 Process for the preparation of combretastatins TGFB2, HMGCR, TGFB1 GAA 1300/4885SNCA 3598/4885ALDH1A1 2753/4885

“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.