Bromide

Bromide

SCHEMBL1731183

Br.N=C1c2nc(C3CC3)ccc2CN1CC(=O)c1ccc(OCC(=O)O)c(C2CCCC2)c1

nearest known ligand 0.44

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 12)

geneUniProtsupporting neighboursconfidence
PTGDR2 Q9Y5Y4 15/20 0.44
PTGDR Q13258 6/20 0.44
PTGER2 P43116 1/20 0.43
PTPN1 P18031 1/20 0.34
KDM4E B2RXH2 2/20 0.33
MAPT P10636 2/20 0.33
RAB9A P51151 2/20 0.33
NPC1 O15118 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.32
SLC6A9 P48067 1/20 0.32
ITGB3 P05106 1/20 0.31
ITGA2B P08514 1/20 0.31

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
SCHEMBL27527319 0.84 KDM4E (0.34) KDM4EMAPTRAB9ANPC1SMN1; SMN2
Bromide SCHEMBL1732707 0.83 F2R (0.36) KDM4EMAPTRAB9ANPC1
Bromide SCHEMBL1731434 0.79 ITGB3 (0.33) KDM4EMAPTRAB9ANPC1SMN1; SMN2
Bromide SCHEMBL5482783 0.78 PTGDR2 (0.33) PTGDR2KDM4EMAPTRAB9ANPC1
Bromide SCHEMBL1732483 0.76 PDE4B (0.34) PTGDR2KDM4EMAPTRAB9ANPC1
Bromide SCHEMBL1730802 0.75 F2R (0.37) KDM4EMAPTRAB9ANPC1
Bromide SCHEMBL1730266 0.75 KDM4E (0.34) KDM4EMAPTRAB9ANPC1
Bromide SCHEMBL1730053 0.75 F2R (0.52) PTGDR2PTGDRPTGER2
Bromide SCHEMBL1729980 0.75 KHK (0.32) KDM4EMAPTRAB9ANPC1
Bromide SCHEMBL1729690 0.74 F2R (0.35) KDM4EMAPTRAB9ANPC1SMN1; 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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1391451-B1 2-IMINOPYRROLIDINE DERIVATES EISAI R&D MAN CO LTD (JP) 2011-11-23 EP disclosed
US-7244730-B2 2-iminopyrrolidine derivatives EISAI CO., LTD (JP) 2007-07-17 US disclosed
US-20050245592-A1 2-Iminopyrrolidine derivatives EISAI R&D MANAGEMENT CO., LTD. (JP) 2005-11-03 US disclosed
US-20050004204-A1 2-Iminopyrrolidine derivatives EISAI R&D MANAGEMENT CO., LTD. (JP) 2005-01-06 US disclosed
EP-1391451-A1 2-IMINOPYRROLIDINE DERIVATES Eisai Co., Ltd. (JP) 2004-02-25 EP 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-20050245592-A1 2-Iminopyrrolidine derivatives H1-2, H1-3, H1-0 PTGDR2 549/4885PTGDR 487/4885PTGER2 1044/4885
US-20050004204-A1 2-Iminopyrrolidine derivatives H1-2, H1-3, H1-0 PTGDR2 544/4885PTGDR 488/4885PTGER2 1028/4885

“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.