Bromide

Bromide

SCHEMBL22263123

Br.Br.N=C(N)SCCc1ccccc1CSC(=N)N

nearest known ligand 0.59

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 18)

geneUniProtsupporting neighboursconfidence
NOS1 P29475 6/20 0.59
IDO1 P14902 8/20 0.59
HTT P42858 4/20 0.59
LMNA P02545 3/20 0.59
SMN1; SMN2 Q16637 2/20 0.59
TAAR1 Q96RJ0 2/20 0.59
BLM P54132 1/20 0.56
NPSR1 Q6W5P4 1/20 0.56
HPGD P15428 1/20 0.56
CYP2D6 P10635 2/20 0.53
NOS3 P29474 2/20 0.53
NOS2 P35228 2/20 0.53
NPC1 O15118 1/20 0.53
CYP3A4 P08684 1/20 0.53
RAB9A P51151 1/20 0.53
HIF1A Q16665 1/20 0.53
SLC11A2 P49281 2/20 0.50
MAPT P10636 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
SCHEMBL22275669 0.98 NOS1 (0.61) NOS1IDO1HTTLMNASMN1; SMN2
Bromide SCHEMBL20920202 0.90 NOS1 (0.53) NOS1IDO1HTTLMNASMN1; SMN2
Bromide SCHEMBL2810146 0.89 IDO1 (0.71) NOS1IDO1HTTLMNASMN1; SMN2
SCHEMBL2812696 0.87 IDO1 (0.74) NOS1IDO1HTTLMNASMN1; SMN2
Bromide SCHEMBL4448055 0.85 NOS1 (0.51) NOS1IDO1HTTLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL22263112 0.85 IDO1 (0.75) NOS1IDO1HTTLMNASMN1; SMN2
SCHEMBL3683034 0.83 NOS1 (0.53) NOS1IDO1HTTLMNASMN1; SMN2
SCHEMBL14068683 0.79 NOS1 (0.59) NOS1IDO1HTTLMNASMN1; SMN2
SCHEMBL9190886 0.79 NOS1 (0.59) NOS1IDO1HTTLMNASMN1; SMN2
SCHEMBL9194773 0.79 NOS1 (0.59) NOS1IDO1HTTLMNASMN1; 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-20250092020-A1 IDO/TDO Inhibitor GENERAL INCORPORATED ASSOCIATION PHARMA VALLEY PROJECT SUPPORTING ORGANIZATION (JP) 2025-03-20 US disclosed
US-12209079-B2 IDO/TDO inhibitor GENERAL INCORPORATED ASSOCIATION PHARMA VALLEY PROJECT SUPPORTING ORGANIZATION (JP) 2025-01-28 US disclosed
US-20220380305-A1 IDO/TDO Inhibitor CANBAS CO., LTD. 2022-12-01 US disclosed
US-20200239452-A1 IDO/TDO Inhibitor CANBAS CO., LTD. (JP) 2020-07-30 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 (4 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-12209079-B2 IDO/TDO inhibitor IDO1, IDO2, TDO2 NOS1 233/4885IDO1 1/4885HTT 71/4885
US-20200239452-A1 IDO/TDO Inhibitor IDO1, IDO2, TDO2 NOS1 233/4885IDO1 1/4885HTT 71/4885
US-20250092020-A1 IDO/TDO Inhibitor IDO1, IDO2, TDO2 NOS1 233/4885IDO1 1/4885HTT 71/4885
US-20220380305-A1 IDO/TDO Inhibitor IDO1, IDO2, TDO2 NOS1 174/4885IDO1 1/4885HTT 100/4885

“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.