Bromide

Bromide

SCHEMBL3866348

Br.N=c1sc2ccccc2n1CC(=O)c1ccc(C2CCCC2)cc1

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 20)

geneUniProtsupporting neighboursconfidence
CYP1A1 P04798 2/20 0.42
CYP1B1 Q16678 2/20 0.42
HAO1 Q9UJM8 1/20 0.41
APAF1 O14727 1/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
KMT2A Q03164 3/20 0.41
ALDH1A1 P00352 2/20 0.41
MEN1 O00255 2/20 0.41
MAPT P10636 2/20 0.41
TP53 P04637 1/20 0.41
CYP3A4 P08684 1/20 0.41
ALOX15 P16050 1/20 0.41
TSHR P16473 1/20 0.41
MAPK1 P28482 1/20 0.41
HSD17B10 Q99714 1/20 0.41
HDAC6 Q9UBN7 1/20 0.41
RAB9A P51151 5/20 0.40
NPC1 O15118 3/20 0.40
LMNA P02545 1/20 0.40
RAD52 P43351 1/20 0.40

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 SCHEMBL11013141 0.83 RAB9A (0.56) SMN1; SMN2KMT2AMEN1MAPTHSD17B10
SCHEMBL13647019 0.81 RAB9A (0.54) SMN1; SMN2KMT2AMEN1MAPTHSD17B10
Bromide SCHEMBL11207242 0.81 CXCR3 (0.57) KMT2AMEN1MAPTTSHRRAB9A
Bromide SCHEMBL3868794 0.81 RAB9A (0.44) CYP1A1CYP1B1SMN1; SMN2KMT2AALDH1A1
SCHEMBL11210832 0.79 CXCR3 (0.59) KMT2AMEN1MAPTRAB9ANPC1
SCHEMBL13650902 0.79 NPC1 (0.57) CYP1A1CYP1B1SMN1; SMN2KMT2AALDH1A1
Bromide SCHEMBL11013450 0.73 CXCR3 (0.60) SMN1; SMN2KMT2AALDH1A1MEN1MAPT
Hydrochloric Acid SCHEMBL6186863 0.70 HTR2A (0.52) SMN1; SMN2KMT2AALDH1A1TSHRRAB9A
SCHEMBL11007835 0.70 GAA (0.46) SMN1; SMN2KMT2AALDH1A1MEN1MAPT
Bromide SCHEMBL962370 0.67 ALDH1A1 (0.57) SMN1; SMN2KMT2AALDH1A1MEN1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7601846-B2 Compounds having activity as inhibitors of apoptosis THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2009-10-13 US disclosed
US-20060122178-A1 Compounds having activity as inhibitors of apoptosis REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE 2006-06-08 US 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-20060122178-A1 Compounds having activity as inhibitors of apoptosis BAD, CASP3, BAX CYP1A1 2365/4885CYP1B1 2548/4885HAO1 4026/4885

“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.