Bromide

Bromide

SCHEMBL5552297

Br.N=C(N)SCc1ccccc1OC(F)(F)F

nearest known ligand 0.53

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 13)

geneUniProtsupporting neighboursconfidence
HTT P42858 4/20 0.53
HPGD P15428 1/20 0.53
IDO1 P14902 10/20 0.51
LMNA P02545 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
TAAR1 Q96RJ0 2/20 0.51
NOS1 P29475 2/20 0.46
NOS3 P29474 1/20 0.46
NOS2 P35228 1/20 0.46
SLC11A2 P49281 2/20 0.44
GRIN2B Q13224 2/20 0.44
GRIN1 Q05586 1/20 0.44
MAPT P10636 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 SCHEMBL4437731 0.82 IDO1 (0.59) HTTHPGDIDO1LMNASMN1; SMN2
SCHEMBL3693822 0.80 IDO1 (0.61) HTTHPGDIDO1LMNASMN1; SMN2
Bromide SCHEMBL2810146 0.78 IDO1 (0.71) HTTHPGDIDO1LMNASMN1; SMN2
SCHEMBL22190951 0.78 IDO1 (0.57) HTTHPGDIDO1LMNASMN1; SMN2
Bromide SCHEMBL17260892 0.76 IDO1 (0.56) HTTHPGDIDO1LMNASMN1; SMN2
SCHEMBL2812696 0.76 IDO1 (0.74) HTTHPGDIDO1LMNASMN1; SMN2
Bromide SCHEMBL4445139 0.75 IDO1 (0.48) HTTHPGDIDO1LMNASMN1; SMN2
SCHEMBL13007589 0.74 IDO1 (0.57) HTTHPGDIDO1LMNASMN1; SMN2
Hydrochloric Acid SCHEMBL22263112 0.74 IDO1 (0.75) HTTHPGDIDO1LMNASMN1; SMN2
SCHEMBL14089893 0.74 IDO1 (0.53) HTTHPGDIDO1LMNASMN1; 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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070015805-A1 Process for preparing 3-arylmethylthio- and 3-heteroarylmethylthio-4,5-dihydroisoxazoline derivatives BAYER CROPSCIENCE GMBH (DE) 2007-01-18 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-20070015805-A1 Process for preparing 3-arylmethylthio- and 3-heteroarylmethylthio-4,5-dihydroisoxazoline derivatives CYP3A7, KMO, CYP4X1 HTT 3186/4885HPGD 3786/4885IDO1 24/4885

“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.