Bromide

Bromide

SCHEMBL1200232

Br.COC(=O)[C@@H](N)CC(F)(F)CC(C)C

nearest known ligand 0.41

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 7)

geneUniProtsupporting neighboursconfidence
MMP8 P22894 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.31
SLC7A5 Q01650 1/20 0.31
KIF11 P52732 1/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 1/20 0.31
SCN9A Q15858 3/20 0.30

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 SCHEMBL1200230 1.00 MMP8 (0.33) MMP8SMN1; SMN2SLC7A5KIF11CA1
SCHEMBL3216912 0.98 MMP8 (0.34) MMP8SMN1; SMN2SLC7A5KIF11CA1
SCHEMBL3216921 0.98 MMP8 (0.34) MMP8SMN1; SMN2SLC7A5KIF11CA1
Hydrochloric Acid SCHEMBL3871144 0.96 MMP8 (0.33) MMP8SMN1; SMN2SLC7A5KIF11CA1
Hydrochloric Acid SCHEMBL3871148 0.96 MMP8 (0.33) MMP8SMN1; SMN2SLC7A5KIF11CA1
Bromide SCHEMBL1199537 0.84 CA1 (0.35) SMN1; SMN2KIF11CA1CA2
Bromide SCHEMBL1199534 0.84 CA1 (0.35) SMN1; SMN2KIF11CA1CA2
SCHEMBL18124775 0.81 CA1 (0.36) SMN1; SMN2KIF11CA1CA2
SCHEMBL8213669 0.81 CA1 (0.36) SMN1; SMN2KIF11CA1CA2
SCHEMBL27857476 0.81 CA1 (0.36) SMN1; SMN2KIF11CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140221478-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS VIROBAY, INC. (US) 2014-08-07 US disclosed
US-8748649-B2 Di-fluoro containing compounds as cysteine protease inhibitors VIROBAY, INC. (US) 2014-06-10 US disclosed
US-8680152-B2 Cathepsin inhibitors for the treatment of bone cancer and bone cancer pain VIROBAY, INC. (US) 2014-03-25 US disclosed
US-20140018421-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS VIROBAY, INC. (US) 2014-01-16 US disclosed
US-8367732-B2 Di-fluoro containing compounds as cysteine protease inhibitors VIROBAY, INC. (US) 2013-02-05 US disclosed
US-20120282267-A1 CATHEPSIN INHIBITORS FOR THE TREATMENT OF BONE CANCER AND BONE CANCER PAIN VIROBAY, INC. (US) 2012-11-08 US disclosed
WO-2012151319-A1 CATHEPSIN INHIBITORS FOR THE TREATMENT OF BONE CANCER AND BONE CANCER PAIN VIROBAY, INC. (US) 2012-11-08 WO disclosed
US-20110172310-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS VIROBAY, INC. (US) 2011-07-14 US disclosed
US-7893112-B2 N-(1-cyanocyclopropyl)-4,4-difluoro-2(S)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino)octamide; rheumatoid arthritis, multiple sclerosis, myasthenia gravis, psoriasis, pemphigus vulgaris, Graves' disease, myasthenia gravis, lupus, asthma, pain, atherosclerosis; cathepsins B, K, L, F, and S inhibitors VIROBAY, INC. (US) 2011-02-22 US disclosed
EP-2262370-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS Virobay, Inc. (US) 2010-12-22 EP disclosed
WO-2009123623-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS VIROBAY, INC. (US) 2009-10-08 WO disclosed
US-20080293819-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS VIROBAY, INC. (US) 2008-11-27 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 (5 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-20080293819-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS CTSF, CTSZ, CTSS MMP8 316/4885SMN1; SMN2 4663/4885SLC7A5 494/4885
US-20120282267-A1 CATHEPSIN INHIBITORS FOR THE TREATMENT OF BONE CANCER AND BONE CANCER PAIN CTSS, CTSB, CTSK MMP8 49/4885SMN1; SMN2 4734/4885SLC7A5 965/4885
US-20140221478-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS CTSF, CTSZ, CTSS MMP8 316/4885SMN1; SMN2 4663/4885SLC7A5 494/4885
US-20110172310-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS CTSF, CTSZ, CTSS MMP8 316/4885SMN1; SMN2 4663/4885SLC7A5 494/4885
US-20140018421-A1 DI-FLUORO CONTAINING COMPOUNDS AS CYSTEINE PROTEASE INHIBITORS CTSF, CTSZ, CTSS MMP8 316/4885SMN1; SMN2 4663/4885SLC7A5 494/4885

“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.