SCHEMBL6296341

SCHEMBL6296341

CC(=O)Nc1nc(C=CC(=O)C(C)C)cs1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.57
HSD17B10 Q99714 2/20 0.57
MAPT P10636 1/20 0.57
L3MBTL1 Q9Y468 1/20 0.48
SMN1; SMN2 Q16637 2/20 0.46
KMT2A Q03164 1/20 0.46
ABL1 P00519 6/20 0.43
PI4KB Q9UBF8 1/20 0.43
NPC1 O15118 4/20 0.42
MAPK1 P28482 1/20 0.42
RAB9A P51151 3/20 0.41
LMNA P02545 1/20 0.41
POLB P06746 1/20 0.41
HDAC3 O15379 1/20 0.40
HDAC4 P56524 1/20 0.40
HDAC1 Q13547 1/20 0.40
HDAC7 Q8WUI4 1/20 0.40
HDAC2 Q92769 1/20 0.40
HDAC10 Q969S8 1/20 0.40
HDAC11 Q96DB2 1/20 0.40

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
SCHEMBL6296340 1.00 KDM4E (0.57) KDM4EHSD17B10MAPTL3MBTL1SMN1; SMN2
SCHEMBL4883820 0.84 KDM4E (0.61) KDM4EHSD17B10MAPTL3MBTL1SMN1; SMN2
SCHEMBL4883834 0.84 KDM4E (0.61) KDM4EHSD17B10MAPTL3MBTL1SMN1; SMN2
SCHEMBL9834015 0.78 KDM4E (0.61) KDM4EHSD17B10MAPTL3MBTL1SMN1; SMN2
SCHEMBL9834016 0.78 KDM4E (0.61) KDM4EHSD17B10MAPTL3MBTL1SMN1; SMN2
SCHEMBL6298271 0.77 HDAC1 (0.49) KDM4ESMN1; SMN2NPC1RAB9APOLB
SCHEMBL6298272 0.77 HDAC1 (0.49) KDM4ESMN1; SMN2NPC1RAB9APOLB
SCHEMBL973060 0.77 KDM4E (0.69) KDM4EHSD17B10MAPTL3MBTL1SMN1; SMN2
SCHEMBL6298520 0.76 HDAC1 (0.41) L3MBTL1SMN1; SMN2HDAC3HDAC4HDAC1
SCHEMBL6298523 0.76 HDAC1 (0.41) L3MBTL1SMN1; SMN2HDAC3HDAC4HDAC1

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 KDM4E 1555/4885HSD17B10 185/4885MAPT 1327/4885
US-20050075390-A1 HIV protease inhibitors DNPEP, PREP, PEPD KDM4E 1634/4885HSD17B10 212/4885MAPT 1198/4885

“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.