Bromide

Bromide

SCHEMBL4940305

Br.CCCCn1c2c(sc1=N)CCCC2

nearest known ligand 0.49

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
CYP1A1 P04798 2/20 0.48
CYP1B1 Q16678 2/20 0.48
RAB9A P51151 12/20 0.48
NPC1 O15118 8/20 0.48
LMNA P02545 7/20 0.48
SMN1; SMN2 Q16637 7/20 0.48
HTT P42858 7/20 0.48
SLC2A1 P11166 5/20 0.48
MEN1 O00255 4/20 0.48
KMT2A Q03164 4/20 0.48
NPSR1 Q6W5P4 4/20 0.48
ALDH1A1 P00352 3/20 0.48
KDM4E B2RXH2 3/20 0.48
PAX8 Q06710 2/20 0.48
NTSR1 P30989 2/20 0.48
NR2F2 P24468 2/20 0.47
CYP3A4 P08684 2/20 0.46
MAPT P10636 2/20 0.46
TP53 P04637 1/20 0.46
ALOX15 P16050 1/20 0.46

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
Bromide SCHEMBL962536 0.79 CYP1A1 (0.47) CYP1A1CYP1B1RAB9ANPC1LMNA
SCHEMBL944243 0.77 RAB9A (0.38) CYP1A1CYP1B1RAB9ANPC1LMNA
Bromide SCHEMBL30145064 0.75 CYP1A1 (0.62) CYP1A1CYP1B1SMN1; SMN2HTTMEN1
SCHEMBL3750688 0.74 RAB9A (0.41) RAB9ANPC1LMNASMN1; SMN2HTT
SCHEMBL5049693 0.74 SMN1; SMN2 (0.43) CYP1A1CYP1B1RAB9ANPC1LMNA
SCHEMBL19610233 0.73 CYP1A1 (0.61) CYP1A1CYP1B1SMN1; SMN2HTTMEN1
Bromide SCHEMBL4939908 0.72 CYP1A1 (0.46) CYP1A1CYP1B1RAB9ASMN1; SMN2MEN1
SCHEMBL6738331 0.70 CYP1A1 (0.45) CYP1A1CYP1B1SMN1; SMN2MEN1KMT2A
Bromide SCHEMBL4940376 0.69 SLC2A1 (0.52) CYP1A1CYP1B1RAB9ANPC1LMNA
SCHEMBL22749443 0.69 SMN1; SMN2 (0.64) CYP1A1CYP1B1RAB9ALMNASMN1; 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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080319032-A1 TETRAHYDROBENZOTHIAZOLE ANALOGUES AS NEUROPROTECTIVE AGENTS GREIG NIGEL H 2008-12-25 US disclosed
US-20040067991-A1 Tetrahydrobenzothiazole analogues as neuroprotective agents GOVERNMENT OF THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES, THE 2004-04-08 US disclosed
EP-1303502-A2 TETRAHYDROBENZOTHIAZOLE ANALOGUES AS NEUROPROTECTIVE AGENTS THE GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2003-04-23 EP disclosed
WO-2002004409-A2 TETRAHYDROBENZOTHIAZOLE ANALOGUES AS NEUROPROTECTIVE AGENTS US GOV HEALTH & HUMAN SERV (US) 2002-01-17 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 (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-20040067991-A1 Tetrahydrobenzothiazole analogues as neuroprotective agents BAX, BAD, BCL2 CYP1A1 2492/4885CYP1B1 1165/4885RAB9A 3179/4885
US-20080319032-A1 TETRAHYDROBENZOTHIAZOLE ANALOGUES AS NEUROPROTECTIVE AGENTS BAX, BAD, BCL2 CYP1A1 2492/4885CYP1B1 1165/4885RAB9A 3179/4885

“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.