SCHEMBL6297901

SCHEMBL6297901

CCOC(=O)CC(=O)C[C@@](O)(CCc1cccc(F)c1C)C(C)C

nearest known ligand 0.39

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
NLRP3 Q96P20 4/20 0.39
ALDH1A1 P00352 4/20 0.36
KMT2A Q03164 2/20 0.35
TAAR1 Q96RJ0 2/20 0.34
LMNA P02545 2/20 0.34
CYP4F2 P78329 2/20 0.34
CYP4A11 Q02928 2/20 0.34
L3MBTL1 Q9Y468 2/20 0.34
SMN1; SMN2 Q16637 1/20 0.33
HSD11B1 P28845 1/20 0.32
KDM4E B2RXH2 1/20 0.32
POLB P06746 1/20 0.32
RIPK1 Q13546 1/20 0.32
MEN1 O00255 1/20 0.32
GAA P10253 1/20 0.32
MAPT P10636 1/20 0.32

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
SCHEMBL6297903 1.00 NLRP3 (0.39) NLRP3ALDH1A1KMT2ATAAR1LMNA
SCHEMBL6302907 0.91 SMN1; SMN2 (0.33) NLRP3ALDH1A1KMT2ATAAR1LMNA
SCHEMBL6297747 0.85 TNF (0.31) ALDH1A1KMT2AKDM4EMEN1
SCHEMBL6297748 0.85 TNF (0.31) ALDH1A1KMT2AKDM4EMEN1
SCHEMBL6296311 0.83 CYP4F2 (0.53) NLRP3ALDH1A1KMT2ALMNACYP4F2
SCHEMBL6296312 0.83 CYP4F2 (0.53) NLRP3ALDH1A1KMT2ALMNACYP4F2
SCHEMBL6699504 0.83 CYP4F2 (0.53) NLRP3ALDH1A1KMT2ALMNACYP4F2
SCHEMBL6296487 0.83 EPHX2 (0.46) ALDH1A1KMT2ACYP4F2CYP4A11L3MBTL1
SCHEMBL6693500 0.81 SLC13A5 (0.40) SMN1; SMN2POLBRIPK1
SCHEMBL6302674 0.81 SLC13A5 (0.40) SMN1; SMN2POLBRIPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040106606-A1 HIV protease inhibitors BOYER FREDERICK EARL (US) 2004-06-03 US claimed
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 claimed
EP-1112269-A2 HIV PROTEASE INHIBITORS WARNER-LAMBERT COMPANY (US) 2001-07-04 EP claimed
WO-2000015634-A2 HIV PROTEASE INHIBITORS WARNER-LAMBERT COMPANY (US) 2000-03-23 WO claimed
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 NLRP3 659/4885ALDH1A1 1219/4885KMT2A 2939/4885
US-20050075390-A1 HIV protease inhibitors DNPEP, PREP, PEPD NLRP3 602/4885ALDH1A1 1309/4885KMT2A 2859/4885

“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.