Bromide

Bromide

SCHEMBL17508351

Br.Cc1ccc2nc3ccccc3cc2c1C

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
▸ ACHE known ✓ P22303 1/20 0.50
▸ P2RY12 known ✓ Q9H244 1/20 0.44
▸ ALDH1A1 P00352 3/20 0.50
▸ HPGD P15428 3/20 0.50
▸ KDM4E B2RXH2 3/20 0.50
▸ GLA P06280 2/20 0.50
▸ GAA P10253 2/20 0.50
▸ NPC1 O15118 1/20 0.50
▸ LMNA P02545 1/20 0.50
▸ POLB P06746 1/20 0.50
▸ PTBP1 P26599 1/20 0.50
▸ RAB9A P51151 1/20 0.50
▸ KMT2A Q03164 1/20 0.50
▸ RCE1 Q9Y256 1/20 0.50
▸ MAPT P10636 1/20 0.50
▸ PDE10A Q9Y233 1/20 0.49
▸ CYP1A2 P05177 3/20 0.48
▸ CYP2A6 P11509 1/20 0.48
▸ TSHR P16473 1/20 0.48
▸ TDP1 Q9NUW8 1/20 0.47

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
SCHEMBL30164507 0.98 ALDH1A1 (0.52) ALDH1A1HPGDKDM4EGLAGAA
SCHEMBL2773901 0.98 ALDH1A1 (0.52) ALDH1A1HPGDKDM4EGLAGAA
SCHEMBL29033070 0.96 ALDH1A1 (0.50) ALDH1A1HPGDKDM4EGLAGAA
Iodide SCHEMBL3905318 0.96 ALDH1A1 (0.50) ALDH1A1HPGDKDM4EGLAGAA
Biphenyl SCHEMBL28506015 0.93 PDE10A (0.54) ALDH1A1HPGDKDM4EGLAGAA
Boric Acid SCHEMBL30999668 0.91 ALDH1A1 (0.46) ALDH1A1HPGDKDM4EGLAGAA
Quinaldine SCHEMBL27595746 0.89 CYP1A2 (0.59) ALDH1A1HPGDKDM4EGLAGAA
SCHEMBL28328127 0.87 ALDH1A1 (0.42) ALDH1A1HPGDKDM4EGLAGAA
Nitric Acid SCHEMBL9696991 0.86 KDM4E (0.48) ALDH1A1HPGDKDM4EGLAGAA
Phenylboronic Acid SCHEMBL28563406 0.86 ALDH1A1 (0.41) ALDH1A1HPGDKDM4EGLAGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108350466-B Methods and compositions for determining pH 芝加哥大学 2022-06-24 — — CN disclosed
US-9676767-B2 Indoloacridine-containing derivative, preparation process and use thereof, and organic luminescent device BOE TECHNOLOGY GROUP CO., LTD. (CN) 2017-06-13 — — US disclosed
US-20160046621-A1 INDOLOACRIDINE-CONTAINING DERIVATIVE, PREPARATION PROCESS AND USE THEREOF, AND ORGANIC LUMINESCENT DEVICE BOE TECHNOLOGY GROUP CO., LTD. (CN) 2016-02-18 — — 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-20160046621-A1 INDOLOACRIDINE-CONTAINING DERIVATIVE, PREPARATION PROCESS AND USE THEREOF, AND ORGANIC LUMINESCENT DEVICE AHR, CDYL, SLC18A1 ACHE 114/4885P2RY12 451/4885ALDH1A1 1979/4885

“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.

Send feedback