Cinnabaramide A

Cinnabaramide A

SCHEMBL208595

CCCCCCC1C(=O)NC2(C(O)C3C=CCCC3)C(=O)OC12C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PSMB5 P28074 16/20 1.00
PSMB1 P20618 10/20 1.00
PSMB2 P49721 10/20 1.00
PSMB11 A5LHX3 9/20 1.00
PSMA7 O14818 9/20 1.00
PSMA1 P25786 9/20 1.00
PSMA2 P25787 9/20 1.00
PSMA3 P25788 9/20 1.00
PSMA4 P25789 9/20 1.00
PSMB8 P28062 9/20 1.00
PSMB9 P28065 9/20 1.00
PSMA5 P28066 9/20 1.00
PSMB4 P28070 9/20 1.00
PSMB6 P28072 9/20 1.00
PSMB10 P40306 9/20 1.00
PSMB3 P49720 9/20 1.00
PSMA6 P60900 9/20 1.00
PSMA8 Q8TAA3 9/20 1.00
PSMB7 Q99436 9/20 1.00

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
Cinnabaramide A SCHEMBL1065927 1.00 PSMB5 (1.00) PSMB5PSMB1PSMB2PSMB11PSMA7
SCHEMBL13618112 1.00 PSMB5 (1.00) PSMB5PSMB1PSMB2PSMB11PSMA7
Cinnabaramide A SCHEMBL1065708 1.00 PSMB5 (1.00) PSMB5PSMB1PSMB2PSMB11PSMA7
Cinnabaramide A SCHEMBL1065711 1.00 PSMB5 (1.00) PSMB5PSMB1PSMB2PSMB11PSMA7
Cinnabaramide A SCHEMBL2714825 1.00 PSMB5 (1.00) PSMB5PSMB1PSMB2PSMB11PSMA7
Cinnabaramide A SCHEMBL16299663 1.00 PSMB5 (1.00) PSMB5PSMB1PSMB2PSMB11PSMA7
SCHEMBL12137121 0.96 PSMB5 (0.93) PSMB5PSMB1PSMB2PSMB11PSMA7
SCHEMBL12137120 0.96 PSMB5 (0.93) PSMB5PSMB1PSMB2PSMB11PSMA7
SCHEMBL6383689 0.92 PSMB5 (0.86) PSMB5PSMB1PSMB2PSMB11PSMA7
SCHEMBL8183419 0.92 PSMB5 (0.85) PSMB5PSMB1PSMB2PSMB11PSMA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8088923-B2 Cyclic-fused beta-lactones and their synthesis THE TEXAS A&M UNIVERSITY SYSTEM (US) 2012-01-03 US disclosed
US-20110015248-A1 SUBSTITUTED HETEROCYCLES INTERMED DISCOVERY GMBH (DE) 2011-01-20 US disclosed
EP-1597262-B1 SUBSTITUTED HETEROCYCLES INTERMED DISCOVERY GMBH (DE) 2009-11-11 EP disclosed
US-20090062547-A1 CYCLIC-FUSED BETA-LACTONES AND THEIR SYNTHESIS THE TEXAS A&M UNIVERSITY SYSTEM 2009-03-05 US disclosed
US-20060229353-A1 Substituted heterocycles INTERMED DISCOVERY GMBH (DE) 2006-10-12 US disclosed
EP-1597262-A2 SUBSTITUTED HETEROCYCLES Bayer HealthCare AG (DE) 2005-11-23 EP disclosed
WO-2004071382-A2 SUBSTITUTED HETEROCYCLES BAYER HEALTHCARE AG (DE) 2004-08-26 WO 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 (3 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-20090062547-A1 CYCLIC-FUSED BETA-LACTONES AND THEIR SYNTHESIS COASY, FASN, OTUB1 PSMB5 7/4885PSMB1 8/4885PSMB2 18/4885
US-20060229353-A1 Substituted heterocycles AHR, LTB4R, LTC4S PSMB5 1824/4885PSMB1 3721/4885PSMB2 3445/4885
US-20110015248-A1 SUBSTITUTED HETEROCYCLES AHR, LTB4R, LTC4S PSMB5 1824/4885PSMB1 3721/4885PSMB2 3445/4885

“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.