SCHEMBL6296830

SCHEMBL6296830

CC(C)C(=O)C=Cc1ccc(F)c(C(F)(F)F)c1

nearest known ligand 0.48

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
APP P05067 7/20 0.48
MAOA P21397 2/20 0.41
MAOB P27338 2/20 0.41
HDAC8 Q9BY41 1/20 0.41
ITGB2 P05107 1/20 0.40
ICAM1 P05362 1/20 0.40
ITGAL P20701 1/20 0.40
GPR183 P32249 1/20 0.39
TAS1R3 Q7RTX0 2/20 0.39
TAS1R1 Q7RTX1 2/20 0.39
TAS1R2 Q8TE23 2/20 0.39
CYP1A2 P05177 1/20 0.38
PTGS2 P35354 1/20 0.38
BACE1 P56817 1/20 0.38
POLB P06746 1/20 0.38
PKM P14618 1/20 0.38
AR P10275 1/20 0.37

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
SCHEMBL6296829 1.00 APP (0.48) APPMAOAMAOBHDAC8ITGB2
SCHEMBL16141410 0.83 IAPP (0.51) APPMAOAMAOBCYP1A2PTGS2
SCHEMBL6298371 0.83 PTGS2 (0.52) APPMAOAMAOBCYP1A2PTGS2
SCHEMBL6298372 0.83 PTGS2 (0.52) APPMAOAMAOBCYP1A2PTGS2
SCHEMBL692664 0.81 KDM4E (0.50) APPMAOAMAOBHDAC8ITGB2
SCHEMBL692665 0.81 KDM4E (0.50) APPMAOAMAOBHDAC8ITGB2
SCHEMBL3277179 0.80 APP (0.48) APPMAOAMAOBHDAC8GPR183
SCHEMBL29470166 0.80 KDR (0.51) APPMAOAMAOBHDAC8GPR183
Hydrochloric Acid SCHEMBL6821092 0.80 KDM4E (0.49) APPMAOAMAOBHDAC8ITGB2
SCHEMBL3277180 0.80 APP (0.48) APPMAOAMAOBHDAC8GPR183

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-20050075390-A1 HIV protease inhibitors AGOURON PHARMACEUTICALS, INC. 2005-04-07 US disclosed
US-6852711-B2 Novel dihydropyrones with tethered heterocycles having improved pharmacologic properties which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The dihydropyrones are useful in the development of therapies for AGOURON PHARMACEUTICALS, INC. (US) 2005-02-08 US disclosed
US-20040106606-A1 HIV protease inhibitors BOYER FREDERICK EARL (US) 2004-06-03 US disclosed
US-6528510-B1 Dihydropyrones with tethered heterocycles; 3-(2-tert-Butyl-4-hydroxymethyl-5-methyl-phenylsulfanyl)-4-hydroxy-6 -isopropyl-6-(2-pyridin-4-yl-ethyl)-5,6-dihydro-pyran - 2-one; WARNER-LAMBERT COMPANY 2003-03-04 US disclosed
EP-1112269-A2 HIV PROTEASE INHIBITORS WARNER-LAMBERT COMPANY (US) 2001-07-04 EP disclosed
WO-2000015634-A2 HIV PROTEASE INHIBITORS WARNER-LAMBERT COMPANY (US) 2000-03-23 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 (2 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-20040106606-A1 HIV protease inhibitors DNPEP, PREP, PEPD APP 123/4885MAOA 2457/4885MAOB 2137/4885
US-20050075390-A1 HIV protease inhibitors DNPEP, PREP, PEPD APP 124/4885MAOA 2595/4885MAOB 2303/4885

“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.