Bromide

Bromide

SCHEMBL2636355

Br.CC(C)(C)OC(=O)N1CCC(NC(=O)Cc2ccc(Br)cc2)CC1

nearest known ligand 0.56

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
SIGMAR1 known ✓ Q99720 1/20 0.55
MEN1 O00255 2/20 0.56
KMT2A Q03164 2/20 0.56
FPR2 P25090 4/20 0.54
FPR3 P25089 2/20 0.54
GPR119 Q8TDV5 2/20 0.53
EPHX1 P07099 1/20 0.52
ALDH1A1 P00352 4/20 0.49
USP30 Q70CQ3 1/20 0.48
HTT P42858 2/20 0.48
NPC1 O15118 1/20 0.48
MAPT P10636 1/20 0.48
MAPK1 P28482 1/20 0.48
RAB9A P51151 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
EPHX2 P34913 1/20 0.47
CA12 O43570 1/20 0.47
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47

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
SCHEMBL2636671 0.99 MEN1 (0.57) MEN1KMT2ASIGMAR1FPR2FPR3
SCHEMBL654137 0.87 LMNA (0.60) MEN1KMT2ASIGMAR1GPR119EPHX1
SCHEMBL3642671 0.87 MEN1 (0.57) MEN1KMT2ASIGMAR1GPR119EPHX1
SCHEMBL4213092 0.86 ALDH1A1 (0.67) MEN1KMT2ASIGMAR1GPR119EPHX1
SCHEMBL23387204 0.85 ALDH1A1 (0.68) MEN1KMT2AGPR119EPHX1ALDH1A1
SCHEMBL3639970 0.84 GPR119 (0.56) MEN1KMT2AGPR119EPHX1ALDH1A1
SCHEMBL5013239 0.83 ALDH1A1 (0.51) MEN1KMT2AFPR2FPR3GPR119
SCHEMBL27706952 0.83 SIGMAR1 (0.59) MEN1KMT2ASIGMAR1GPR119EPHX1
SCHEMBL22255024 0.81 ALDH1A1 (0.60) MEN1KMT2ASIGMAR1FPR2FPR3
SCHEMBL18129124 0.81 FPR2 (0.49) FPR2FPR3GPR119EPHX1ALDH1A1

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-8754095-B2 Substituted N-heterocycloalkyl bipyrrolidinylphenyl amide derivatives, preparation and therapeutic use thereof SANOFI (FR) 2014-06-17 US disclosed
EP-2569297-A1 SUBSTITUTED N-HETEROCYCLOALKYL BIPYRROLIDINYLPHENYL AMIDE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI (FR) 2013-03-20 EP disclosed
US-20130059891-A1 SUBSTITUTED N-HETEROCYCLOALKYL BIPYRROLIDINYLPHENYL AMIDE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI (FR) 2013-03-07 US disclosed
WO-2011143161-A1 SUBSTITUTED N-HETEROCYCLOALKYL BIPYRROLIDINYLPHENYL AMIDE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI (FR) 2011-11-17 WO 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-20130059891-A1 SUBSTITUTED N-HETEROCYCLOALKYL BIPYRROLIDINYLPHENYL AMIDE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF HRH3, HRH4, HRH1 SIGMAR1 128/4885MEN1 3792/4885KMT2A 489/4885

“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.