Bromide

Bromide

SCHEMBL11288446

Br.C=CCN1CCc2cc(O)c(O)cc2C(c2ccccc2)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
▸ KDM4E B2RXH2 5/20 1.00
▸ BLM P54132 4/20 1.00
▸ PMP22 Q01453 4/20 1.00
▸ LMNA P02545 3/20 1.00
▸ DRD1 P21728 11/20 0.98
▸ MAPT P10636 5/20 0.98
▸ MTOR P42345 3/20 0.98
▸ CYP2D6 P10635 3/20 0.98
▸ THPO P40225 3/20 0.98
▸ HIF1A Q16665 3/20 0.98
▸ HSD17B10 Q99714 3/20 0.98
▸ TDP1 Q9NUW8 1/20 0.98
▸ DRD2 P14416 6/20 0.83
▸ DRD5 P21918 1/20 0.72
▸ GMNN O75496 2/20 0.68
▸ GAA P10253 1/20 0.68
▸ PKM P14618 1/20 0.68
▸ GFER P55789 1/20 0.68
▸ CYP1A2 P05177 2/20 0.66
▸ CYP3A4 P08684 2/20 0.66

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
SCHEMBL7390591 0.99 DRD1 (1.00) KDM4EBLMPMP22LMNADRD1
Hydrochloric Acid SCHEMBL7203243 0.98 DRD1 (1.00) KDM4EBLMPMP22LMNADRD1
SCHEMBL10745918 0.85 DRD1 (0.75) KDM4EBLMPMP22LMNADRD1
Hydrochloric Acid SCHEMBL10747243 0.84 DRD1 (0.76) KDM4EBLMPMP22LMNADRD1
SCHEMBL11605631 0.84 DRD2 (0.76) KDM4EBLMPMP22LMNADRD1
Bromide SCHEMBL11539891 0.84 KDM4E (0.72) KDM4EBLMPMP22LMNADRD1
Hydrochloric Acid SCHEMBL10345839 0.83 DRD1 (0.74) KDM4EBLMPMP22LMNADRD1
SCHEMBL14510732 0.82 DRD1 (0.82) KDM4EBLMPMP22LMNADRD1
Bromide SCHEMBL11721722 0.82 KDM4E (0.71) KDM4EBLMPMP22LMNADRD1
SCHEMBL11157379 0.81 DRD1 (0.70) KDM4EBLMPMP22LMNADRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190015423-A1 REGULATION OF GENE EXPRESSION BY MODULATING PRIMARY CILIA LENGTH NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2019-01-17 — — US claimed
EP-2806276-A1 Method for post mortem diagnosis of Alzheimer's Disease (AD) Red Bull GmbH (AT) 2014-11-26 — — EP claimed
US-20190015423-A1 REGULATION OF GENE EXPRESSION BY MODULATING PRIMARY CILIA LENGTH NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2019-01-17 — — US disclosed
EP-2806276-A1 Method for post mortem diagnosis of Alzheimer's Disease (AD) Red Bull GmbH (AT) 2014-11-26 — — EP disclosed
US-4342686-A Intermediates for preparing 6-lower alkyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines SMITHKLINE CORPORATION (US) 1982-08-03 — — US disclosed
US-4265889-A DOPAMINERGIC, HYPOTENSIVE SMITHKLINE CORPORATION (US) 1981-05-05 — — US disclosed
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