Bromide

Bromide

SCHEMBL7687716

Br.O=S(=O)(NCCCc1ccccc1)c1cc(Cl)c2cccnc2c1O

nearest known ligand 0.50

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
HTR1A known ✓ P08908 1/20 0.45
SLC6A2 known ✓ P23975 1/20 0.45
ALDH1A1 P00352 6/20 0.50
KDM4E B2RXH2 4/20 0.50
TDP1 Q9NUW8 3/20 0.50
CYP3A4 P08684 2/20 0.50
CYP1A2 P05177 1/20 0.50
CYP2C9 P11712 1/20 0.50
MAPK1 P28482 1/20 0.50
CYP2C19 P33261 1/20 0.50
SMN1; SMN2 Q16637 2/20 0.49
TP53 P04637 2/20 0.46
GAA P10253 1/20 0.46
MMP14 P50281 2/20 0.45
KMT2A Q03164 5/20 0.45
MEN1 O00255 4/20 0.45
HSP90AA1 P07900 4/20 0.45
MMP9 P14780 3/20 0.45
ALOX15B O15296 1/20 0.45
NR1I2 O75469 1/20 0.45

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
SCHEMBL7787448 0.86 KDM4E (0.64) ALDH1A1KDM4ETDP1CYP3A4SMN1; SMN2
SCHEMBL7684993 0.86 ALDH1A1 (0.48) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL7691072 0.85 KMT2A (0.62) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL7691423 0.83 TDP1 (0.50) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL7686834 0.80 ALDH1A1 (0.52) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL7685023 0.78 ALDH1A1 (0.61) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL8311550 0.77 MAPT (0.49) ALDH1A1SMN1; SMN2GAAMAPTHTT
SCHEMBL10908982 0.73 MEN1 (0.64) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL7689196 0.73 KDM4E (0.64) ALDH1A1KDM4ETDP1CYP3A4CYP1A2
SCHEMBL7684587 0.73 KDM4E (0.64) ALDH1A1KDM4ETDP1CYP3A4CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6211376-B1 HERPES VIRUS, CYTOMEGALO VIRUS, VARICELLA-ZOSTER VIRUS,EPSTEIN-BARR VIRUS PHARMACIA & UPJOHN COMPANY 2001-04-03 US claimed
EP-0927164-A1 8-HYDROXY-7-SUBSTITUTED QUINOLINES AS ANTI-VIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 1999-07-07 EP claimed
WO-1998011073-A1 8-HYDROXY-7-SUBSTITUTED QUINOLINES AS ANTI-VIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 1998-03-19 WO claimed
US-6500842-B1 N-((4-CHLOROPHENYL)METHYL)-8-HYDROXY-7-QUINOLINECARBOXAMIDE ADMINISTERED AS VIRICIDES AGAINST HERPES VIRUS PHARMACIA & UPJOHN COMPANY 2002-12-31 US disclosed
US-6310211-B1 ANTI-VIRAL ACTIVITY AGAINST HERPES VIRUS, CYTOMEGALOVIRUS. MANY OF THESE COMPOUNDS ARE ALSO ACTIVE AGAINST VARICELLA ZOSTER VIRUS, EPSTEIN-BARR VIRUS, HERPES SIMPLEX VIRUS AND HUMAN HERPES VIRUS TYPE 8 PHARMACIA & UPJOHN COMPANY 2001-10-30 US disclosed
US-6252080-B1 HERPES, CYTOMEGALO VIRUS PHARMACIA & UPJOHN COMPANY 2001-06-26 US disclosed
US-6211376-B1 HERPES VIRUS, CYTOMEGALO VIRUS, VARICELLA-ZOSTER VIRUS,EPSTEIN-BARR VIRUS PHARMACIA & UPJOHN COMPANY 2001-04-03 US disclosed
EP-0927164-A1 8-HYDROXY-7-SUBSTITUTED QUINOLINES AS ANTI-VIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 1999-07-07 EP disclosed
WO-1998011073-A1 8-HYDROXY-7-SUBSTITUTED QUINOLINES AS ANTI-VIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 1998-03-19 WO disclosed