SCHEMBL2723964

SCHEMBL2723964

Cc1occc1B1OC(C)(C)C(C)(C)O1

nearest known ligand 0.40

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LPL P06858 12/20 0.40
LIPG Q9Y5X9 12/20 0.40
P2RX7 Q99572 1/20 0.37
KDM4E B2RXH2 1/20 0.32
LMNA P02545 1/20 0.32
ALOX5 P09917 1/20 0.32
CA1 P00915 2/20 0.32
CA2 P00918 2/20 0.32
CA9 Q16790 2/20 0.32
CA12 O43570 1/20 0.32
CA3 P07451 1/20 0.32
CA4 P22748 1/20 0.32
CA6 P23280 1/20 0.32
CA5A P35218 1/20 0.32
CA7 P43166 1/20 0.32
CA14 Q9ULX7 1/20 0.32
CA5B Q9Y2D0 1/20 0.32
MAPK1 P28482 1/20 0.32
F11 P03951 1/20 0.31

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
SCHEMBL826713 0.79 LPL (0.40) LPLLIPGP2RX7CA1CA2
SCHEMBL22886631 0.78 LPL (0.39) LPLLIPGP2RX7CA1CA2
SCHEMBL13906124 0.74
SCHEMBL14746261 0.73 LPL (0.36) LPLLIPGP2RX7CA1CA2
SCHEMBL12703333 0.73 LPL (0.42) LPLLIPGP2RX7CA1CA2
SCHEMBL5134635 0.72 F11 (0.38) LPLLIPGP2RX7KDM4ECA1
SCHEMBL23031438 0.71 LPL (0.40) LPLLIPGP2RX7CA1CA2
SCHEMBL13905386 0.71 KDM4E (0.32) KDM4ELMNAALOX5
SCHEMBL12566009 0.71 LPL (0.37) LPLLIPGP2RX7
SCHEMBL5899734 0.70 LPL (0.54) LPLLIPGP2RX7CA1CA2

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 73 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250313567-A1 IMIDAZOPYRIMIDINES AND TRIAZOLOPYRIMIDINES AS A2A / A2B INHIBITORS INCYTE CORPORATION 2025-10-09 US disclosed
US-20240374582-A1 SELECTIVE INHIBITORS OF ROCK1 AND ROCK2 PROTEIN KINASES AND THEIR USES THEREOF Genosco Inc. 2024-11-14 US disclosed
US-12116369-B2 Substituted pyrazolo[1,5-a]pyrimidines as glucocerebrosidase activators Bial—R&D Investments, S.A. (PT) 2024-10-15 US disclosed
CN-118666828-A Triazine compound and application thereof in medicines 广东东阳光药业股份有限公司 2024-09-20 CN disclosed
US-12064426-B2 Selective inhibitors of ROCK1 and ROCK2 protein kinases and uses thereof Genosco Inc. (US) 2024-08-20 US disclosed
CN-117903140-A Imidazopyrimidines and triazolopyrimidines as A2A/A2B inhibitors 因赛特公司 2024-04-19 CN disclosed
CN-117136186-A Selective inhibitors of ROCK1 and ROCK2 protein kinases and uses thereof 盖诺斯克公司 2023-11-28 CN disclosed
EP-4274825-A1 SELECTIVE INHIBITORS OF ROCK1 AND ROCK2 PROTEIN KINASES AND USES THEREOF Genosco Inc. (US) 2023-11-15 EP disclosed
US-20230357255-A1 IMIDAZOPYRIMIDINES AND TRIAZOLOPYRIMIDINES AS A2A / A2B INHIBITORS INCYTE CORPORATION 2023-11-09 US disclosed
US-11673894-B2 Imidazopyrimidines and triazolopyrimidines as A2A / A2B inhibitors INCYTE CORPORATION (US) 2023-06-13 US disclosed
WO-2009032653-A1 INHIBITORS OF AKT ACTIVITY SMITH KLINE BEECHAM CORPORATION (US) 2009-03-12 WO disclosed
WO-2009032653-A1 INHIBITORS OF AKT ACTIVITY SMITH KLINE BEECHAM CORPORATION (US) 2009-03-12 WO disclosed
WO-2009032651-A1 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORPORATION (US) 2009-03-12 WO disclosed
WO-2009032651-A1 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORPORATION (US) 2009-03-12 WO disclosed
WO-2009032652-A1 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORPORATION (US) 2009-03-12 WO disclosed
WO-2009032652-A1 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORPORATION (US) 2009-03-12 WO disclosed
EP-1720855-A4 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORP (US) 2008-12-17 EP disclosed
US-20070185152-A1 Inhibitors of akt activity SMITHKLINE BEECHAM CORPORATION 2007-08-09 US disclosed
EP-1720855-A1 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORPORATION (US) 2006-11-15 EP disclosed
WO-2005085227-A1 INHIBITORS OF AKT ACTIVITY SMITHKLINE BEECHAM CORPORATION (US) 2005-09-15 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 (7 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-12064426-B2 Selective inhibitors of ROCK1 and ROCK2 protein kinases and uses thereof ROCK2, ROCK1, MYLK3 LPL 4675/4885LIPG 2908/4885P2RX7 4381/4885
US-12116369-B2 Substituted pyrazolo[1,5-a]pyrimidines as glucocerebrosidase activators GBA1, GALC, GBA3 LPL 295/4885LIPG 1458/4885P2RX7 213/4885
US-20070185152-A1 Inhibitors of akt activity AKT1, AKT1S1, AKT2 LPL 3809/4885LIPG 4263/4885P2RX7 1783/4885
US-20230357255-A1 IMIDAZOPYRIMIDINES AND TRIAZOLOPYRIMIDINES AS A2A / A2B INHIBITORS ADORA2A, ADORA2B, ADORA1 LPL 4054/4885LIPG 3519/4885P2RX7 9/4885
US-11673894-B2 Imidazopyrimidines and triazolopyrimidines as A2A / A2B inhibitors ADORA2A, ADORA2B, ADORA1 LPL 4054/4885LIPG 3519/4885P2RX7 9/4885
US-20240374582-A1 SELECTIVE INHIBITORS OF ROCK1 AND ROCK2 PROTEIN KINASES AND THEIR USES THEREOF ROCK2, ROCK1, MYLK3 LPL 4709/4885LIPG 2967/4885P2RX7 4438/4885
US-20250313567-A1 IMIDAZOPYRIMIDINES AND TRIAZOLOPYRIMIDINES AS A2A / A2B INHIBITORS ADORA2A, ADORA2B, ADORA1 LPL 4054/4885LIPG 3519/4885P2RX7 9/4885

“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.