Bromide

Bromide

SCHEMBL3204595

Br.CC(=N)Nc1ccc2[nH]c(-c3cccc(C(F)(F)F)c3)nc2c1

nearest known ligand 0.47

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
KDM4E B2RXH2 6/20 0.47
MEN1 O00255 4/20 0.47
KMT2A Q03164 4/20 0.47
ALDH1A1 P00352 3/20 0.47
SMN1; SMN2 Q16637 3/20 0.47
HPGD P15428 2/20 0.47
HSD17B10 Q99714 2/20 0.47
POLB P06746 2/20 0.47
TP53 P04637 2/20 0.47
CYP1A2 P05177 2/20 0.45
CYP3A4 P08684 2/20 0.45
CYP2C9 P11712 2/20 0.45
CYP2C19 P33261 1/20 0.45
PARP1 P09874 1/20 0.45
PIN1 Q13526 1/20 0.45
PDPK1 O15530 1/20 0.44
NPBWR1 P48145 1/20 0.44
NPC1 O15118 2/20 0.44
THRB P10828 2/20 0.44
RAB9A P51151 2/20 0.44

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
SCHEMBL6518096 0.99 KDM4E (0.48) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL13343686 0.82 KDM4E (0.53) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL13420281 0.82 KDM4E (0.51) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL13343681 0.78 KDM4E (0.50) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL3201303 0.77 NPBWR1 (0.58) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
Hydrochloric Acid SCHEMBL3202338 0.77 KDM4E (0.49) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL13420244 0.77 EGFR (0.54) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL3203000 0.76 KDM4E (0.46) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL3182326 0.76 KDM4E (0.56) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2
SCHEMBL3198870 0.75 MEN1 (0.57) KDM4EMEN1KMT2AALDH1A1SMN1; SMN2

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-20100120802-A1 Novel Anti-Inflammatory and Analgesic Heterocyclic Amidines that Inhibit Nitrogen Oxide (NO) Production MAKOVEC FRANCESCO 2010-05-13 US disclosed
US-7674809-B2 Anti-inflammatory and analgesic heterocyclic amidines that inhibit nitrogen oxide (NO) production ROTTAPHARM S.P.A. (IT) 2010-03-09 US disclosed
US-20050197331-A1 Novel anti-inflammatory and analgesic heterocyclic amidines that inhibit nitrogen oxide (NO) production ROTTAPHARM SPA 2005-09-08 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-20100120802-A1 Novel Anti-Inflammatory and Analgesic Heterocyclic Amidines that Inhibit Nitrogen Oxide (NO) Production NOS3, NOS1, NOS2 KDM4E 3052/4885MEN1 3366/4885KMT2A 3630/4885
US-20050197331-A1 Novel anti-inflammatory and analgesic heterocyclic amidines that inhibit nitrogen oxide (NO) production NOS3, NOS1, NOS2 KDM4E 3052/4885MEN1 3366/4885KMT2A 3630/4885

“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.