Bromide

Bromide

SCHEMBL9549584

CN(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)Cc1ccccc1.[Br-]

nearest known ligand 0.55

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 17)

geneUniProtsupporting neighboursconfidence
▸ CARM1 Q86X55 1/20 0.55
▸ PRMT6 Q96LA8 1/20 0.55
▸ PRMT8 Q9NR22 1/20 0.55
▸ SIGMAR1 Q99720 2/20 0.50
▸ HIF1A Q16665 1/20 0.48
▸ TSHR P16473 3/20 0.45
▸ ALDH1A1 P00352 3/20 0.45
▸ MAOB P27338 4/20 0.44
▸ LMNA P02545 3/20 0.44
▸ MAOA P21397 2/20 0.44
▸ USP2 O75604 1/20 0.44
▸ CYP3A4 P08684 1/20 0.44
▸ PYCR1 P32322 1/20 0.44
▸ SMN1; SMN2 Q16637 3/20 0.43
▸ BLM P54132 1/20 0.43
▸ AOC3 Q16853 1/20 0.42
▸ KDM4E B2RXH2 1/20 0.42

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
Hydrochloric Acid SCHEMBL9549758 0.96 CARM1 (0.55) CARM1PRMT6PRMT8SIGMAR1HIF1A
Phosphoric Acid SCHEMBL9549658 0.89 SIGMAR1 (0.47) CARM1PRMT6PRMT8SIGMAR1HIF1A
Acetic Acid SCHEMBL9549681 0.88 CARM1 (0.46) CARM1PRMT6PRMT8SIGMAR1TSHR
Bromide SCHEMBL143506 0.79 HIF1A (0.58) HIF1ATSHRALDH1A1LMNASMN1; SMN2
SCHEMBL7055109 0.78 CARM1 (0.75) CARM1PRMT6PRMT8SIGMAR1TSHR
SCHEMBL8297797 0.78 HTR2A (0.62) CARM1PRMT6PRMT8SIGMAR1TSHR
SCHEMBL14578374 0.76 CARM1 (0.60) CARM1PRMT6PRMT8SIGMAR1TSHR
SCHEMBL9750655 0.75 HTR2A (0.58) CARM1PRMT6PRMT8SIGMAR1TSHR
Iodide SCHEMBL9549744 0.75 HIF1A (0.58) HIF1ATSHRALDH1A1LMNASMN1; SMN2
Hydrochloric Acid SCHEMBL9549567 0.75 HIF1A (0.58) SIGMAR1HIF1ATSHRALDH1A1LMNA

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-5208317-A Molding materials of cured epoxy resins THE DOW CHEMICAL COMPANY (US) 1993-05-04 — — US disclosed
US-5109099-A ADVANCING EPOXY RESINS IN PRESENCE OF AMINO GROUP-CONTAINING PHOSPHONIUM CATALYST THE DOW CHEMICAL COMPANY (US) 1992-04-28 — — US disclosed
EP-0441243-A2 Precatalyzed catalyst compositions, process for preparing epoxy resins, curable compositions, articles resulting from curing the resultant compositions THE DOW CHEMICAL COMPANY (US) 1991-08-14 — — EP disclosed
US-4981926-A Rapid and selective curing using phosphonium catalyst containing an amine group; polyepoxides THE DOW CHEMICAL COMPANY (US) 1991-01-01 — — US disclosed
Send feedback