SCHEMBL6298486

SCHEMBL6298486

CC(C)c1cc2nc(N)sc2cc1SC1=C(O)C[C@@](CCc2ccccc2)(C(C)C)OC1=O

nearest known ligand 0.35

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 3/20 0.35
LDHA P00338 9/20 0.33
LDHB P07195 4/20 0.33
DRD2 P14416 2/20 0.33
KCNH2 Q12809 1/20 0.33
CYP2D6 P10635 2/20 0.33
CYP2C9 P11712 1/20 0.32
CYP2C19 P33261 1/20 0.32
WRN Q14191 1/20 0.31
NPC1 O15118 1/20 0.30
SCN4A P35499 1/20 0.30
RAB9A P51151 1/20 0.30
SMN1; SMN2 Q16637 1/20 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
SCHEMBL6298488 1.00 CYP3A4 (0.35) CYP3A4LDHALDHBDRD2KCNH2
SCHEMBL6302772 0.94 GAA (0.31) NPC1SCN4ARAB9ASMN1; SMN2
SCHEMBL6302779 0.94 GAA (0.31) NPC1SCN4ARAB9ASMN1; SMN2
SCHEMBL6303150 0.90 CYP3A4 (0.33) CYP3A4LDHALDHBDRD2KCNH2
SCHEMBL6303151 0.90 CYP3A4 (0.33) CYP3A4LDHALDHBDRD2KCNH2
SCHEMBL6297753 0.89 DRD2 (0.32) DRD2KCNH2
SCHEMBL6302845 0.88 HSD11B1 (0.30) LDHALDHB
SCHEMBL6296814 0.85 LDHA (0.35) LDHALDHB
SCHEMBL6296817 0.85 LDHA (0.35) LDHALDHB
SCHEMBL6296818 0.84 GAA (0.30)

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 CYP3A4 247/4885LDHA 1807/4885LDHB 1604/4885
US-20050075390-A1 HIV protease inhibitors DNPEP, PREP, PEPD CYP3A4 273/4885LDHA 1791/4885LDHB 1624/4885

“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.