Bromide

Bromide

SCHEMBL3916334

Cc1cc[n+](CCCCCC(=O)O)c2c(C)cccc12.[Br-]

nearest known ligand 0.54

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
POLB P06746 2/20 0.54
KDM4E B2RXH2 1/20 0.54
RECQL P46063 1/20 0.41
PARP1 P09874 1/20 0.36
PARP2 Q9UGN5 1/20 0.36
SMN1; SMN2 Q16637 2/20 0.36
KMT2A Q03164 2/20 0.36
MEN1 O00255 1/20 0.36
ALDH1A1 P00352 1/20 0.36
GFER P55789 1/20 0.36
HSD17B10 Q99714 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
EGFR P00533 2/20 0.36
MAPT P10636 2/20 0.36
RXFP1 Q9HBX9 1/20 0.36
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36
HDAC3 O15379 1/20 0.36
HDAC4 P56524 1/20 0.36
HDAC1 Q13547 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
SCHEMBL7069821 0.99 KDM4E (0.52) POLBKDM4ERECQLPARP1PARP2
SCHEMBL6833605 0.84 POLB (0.46) POLBKDM4ERECQLSMN1; SMN2KMT2A
Bromide SCHEMBL3915979 0.83 KDM4E (0.80) POLBKDM4ERECQLSMN1; SMN2KMT2A
SCHEMBL1105809 0.81 KDM4E (0.77) POLBKDM4ERECQLSMN1; SMN2KMT2A
Iodide SCHEMBL2057098 0.80 KDM4E (0.75) POLBKDM4ERECQLSMN1; SMN2KMT2A
SCHEMBL15419914 0.80 KDM4E (0.79) POLBKDM4ERECQLSMN1; SMN2KMT2A
Bromide SCHEMBL3916333 0.75 KDM4E (0.56) POLBKDM4ERECQLSMN1; SMN2KMT2A
SCHEMBL16663887 0.75 KDM4E (0.81) POLBKDM4ERECQLSMN1; SMN2KMT2A
SCHEMBL7069818 0.74 KDM4E (0.54) POLBKDM4ERECQLSMN1; SMN2KMT2A
Bromide SCHEMBL285416 0.72 POLB (0.72) POLBKDM4ESMN1; SMN2KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7563907-B2 Compounds based on polymethines DYOMICS GMBH (DE) 2009-07-21 US disclosed
US-20040260093-A1 Compound, especially marker-dye on the basis of polymethines DYOMICS GMBH (DE) 2004-12-23 US disclosed
US-20030165942-A1 Compound, especially marker-dye, on the basis of polymethines DYOMICS GMBH (DE) 2003-09-04 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 (2 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-20030165942-A1 Compound, especially marker-dye, on the basis of polymethines MKI67, CYBA, IK POLB 1040/4885KDM4E 2432/4885RECQL 1536/4885
US-20040260093-A1 Compound, especially marker-dye on the basis of polymethines MKI67, IK, CYBA POLB 838/4885KDM4E 2399/4885RECQL 1491/4885

“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.