Bromide

Bromide

SCHEMBL6480413

Br.Cn1ccc2ccccc21

nearest known ligand 0.54

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
CDK4 P11802 4/20 0.54
CCND1 P24385 4/20 0.54
ALDH1A1 P00352 2/20 0.48
MAPT P10636 2/20 0.48
KDM4E B2RXH2 1/20 0.48
RXFP1 Q9HBX9 1/20 0.48
PRKCI P41743 1/20 0.48
HTR2A P28223 1/20 0.47
HTR2C P28335 1/20 0.47
NOTUM Q6P988 1/20 0.47
NQO2 P16083 1/20 0.47
CA12 O43570 2/20 0.45
CA9 Q16790 2/20 0.45
BRD4 O60885 1/20 0.45
BRPF1 P55201 1/20 0.45
KAT2B Q92831 1/20 0.45
BRD9 Q9H8M2 1/20 0.45
CYP2A6 P11509 2/20 0.44
HSD11B1 P28845 1/20 0.43
BIRC5 O15392 1/20 0.41

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 SCHEMBL31591097 1.00 CDK4 (0.54) CDK4CCND1ALDH1A1MAPTKDM4E
SCHEMBL29384135 0.97 CDK4 (0.56) CDK4CCND1ALDH1A1MAPTKDM4E
SCHEMBL29812 0.97 CDK4 (0.56) CDK4CCND1ALDH1A1MAPTKDM4E
Hydrochloric Acid SCHEMBL1356443 0.95 CDK4 (0.54) CDK4CCND1ALDH1A1MAPTKDM4E
Hydrochloric Acid SCHEMBL30610362 0.95 CDK4 (0.54) CDK4CCND1ALDH1A1MAPTKDM4E
Formaldehyde SCHEMBL27911684 0.91 CDK4 (0.50) CDK4CCND1ALDH1A1MAPTKDM4E
Dimethylamine SCHEMBL3332471 0.91 CDK4 (0.50) CDK4CCND1ALDH1A1MAPTKDM4E
Methylene Chloride SCHEMBL29003670 0.89 CDK4 (0.54) CDK4CCND1ALDH1A1MAPTKDM4E
SCHEMBL1606641 0.89 CDK4 (0.48) CDK4CCND1ALDH1A1MAPTKDM4E
SCHEMBL9245607 0.87 HTR2A (0.47) CDK4CCND1ALDH1A1MAPTKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050154039-A1 5-Sulphanyl-4h-1,2,4-triazole derivatives and their use as medicine IPSEN PHARMA S.A.S. (FR) 2005-07-14 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-20050154039-A1 5-Sulphanyl-4h-1,2,4-triazole derivatives and their use as medicine SSTR3, SSTR1, SSTR5 CDK4 384/4885CCND1 812/4885ALDH1A1 2784/4885

“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.