SCHEMBL4132567

SCHEMBL4132567

CC(C)(C)OC(=O)N[C@@H]1CN(C(=O)OCc2ccccc2)CC[C@H]1F

nearest known ligand 0.55

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PDE4B Q07343 1/20 0.55
SMN1; SMN2 Q16637 3/20 0.49
NPC1 O15118 2/20 0.49
RAB9A P51151 2/20 0.49
HTT P42858 1/20 0.48
CYP2C19 P33261 1/20 0.47
USP30 Q70CQ3 1/20 0.47
L3MBTL1 Q9Y468 2/20 0.44
KMT2A Q03164 1/20 0.44
HSD11B1 P28845 1/20 0.44
GRIN2B Q13224 1/20 0.44
DPP4 P27487 1/20 0.43
KCNH2 Q12809 1/20 0.43
DPP7 Q9UHL4 1/20 0.43

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
SCHEMBL17426118 1.00 PDE4B (0.55) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL4132542 1.00 PDE4B (0.55) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL21335543 1.00 PDE4B (0.55) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL28950424 1.00 PDE4B (0.55) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL11916326 1.00 PDE4B (0.55) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL23191704 1.00 PDE4B (0.55) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL14801009 0.93 SMN1; SMN2 (0.53) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL1468571 0.92 USP30 (0.52) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL1468570 0.92 USP30 (0.52) PDE4BSMN1; SMN2NPC1RAB9AHTT
SCHEMBL31520766 0.92 PDE4B (0.53) PDE4BSMN1; SMN2NPC1RAB9AHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230405002-A1 COMBINATIONS OF DIACYLGLYCEROL ACYLTRANSFERASE 2 INHIBITORS AND ACETYL-COA CARBOXYLASE INHIBITOR PFIZER INC. (US) 2023-12-21 US disclosed
EP-4038060-B1 DIACYLGLYCEROL ACYLTRANSFERASE 2 INHIBITOR PFIZER (US) 2023-11-15 EP disclosed
US-11471458-B2 Diacylglycerol acyl transferase 2 inhibitor PFIZER INC. (US) 2022-10-18 US disclosed
US-11471458-B2 Diacylglycerol acyl transferase 2 inhibitor PFIZER INC. (US) 2022-10-18 US disclosed
US-11065249-B2 Diacylglycerol acyl transferase 2 inhibitor PFIZER INC. (US) 2021-07-20 US disclosed
US-20210100796-A1 DIACYLGLYCEROL ACYL TRANSFERASE 2 INHIBITOR PFIZER INC. (US) 2021-04-08 US disclosed
US-20210100798-A1 DIACYLGLYCEROL ACYL TRANSFERASE 2 INHIBITOR PFIZER INC. (US) 2021-04-08 US disclosed
US-8829193-B2 PIM kinase inhibitors and methods of their use NOVARTIS AG (CH) 2014-09-09 US disclosed
US-20140249135-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE NOVARTIS AG (CH) 2014-09-04 US disclosed
US-8822497-B2 PIM kinase inhibitors and methods of their use NOVARTIS AG (CH) 2014-09-02 US disclosed
US-20120208815-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE NOVARTIS AG (CH) 2012-08-16 US disclosed
US-20120202851-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE NOVARTIS AG (CH) 2012-08-09 US disclosed
US-8168794-B2 Pim kinase inhibitors and methods of their use NOVARTIS AG (CH) 2012-05-01 US disclosed
US-20110195956-A1 Heterocyclic Kinase Inhibitors NOVARTIS AG (CH) 2011-08-11 US disclosed
US-20110195980-A1 Bicyclic Kinase Inhibitors NOVARTIS AG (CH) 2011-08-11 US disclosed
US-20100216839-A1 Pim kinase inhibitors and methods of their use NOVARTIS AG (CH) 2010-08-26 US disclosed
WO-2010026122-A1 HETEROCYCLIC PIM-KINASE INHIBITORS NOVARTIS AG (CH) 2010-03-11 WO disclosed
WO-2010026121-A1 BICYCLIC KINASE INHIBITORS NOVARTIS AG (CH) 2010-03-11 WO disclosed
WO-2009109576-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE NOVARTIS AG (CH) 2009-09-11 WO disclosed
WO-2008106692-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE NOVARTIS VACCINES AND DIAGNOSTICS, INC. (US) 2008-09-04 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 (11 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-11065249-B2 Diacylglycerol acyl transferase 2 inhibitor DGAT2, DGAT1, ACAT2 PDE4B 817/4885SMN1; SMN2 4817/4885NPC1 192/4885
US-20100216839-A1 Pim kinase inhibitors and methods of their use PIM1, PIM2, PIM3 PDE4B 1716/4885SMN1; SMN2 3818/4885NPC1 1582/4885
US-20140249135-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE PIM1, PIM2, PIM3 PDE4B 2918/4885SMN1; SMN2 2557/4885NPC1 4325/4885
US-20230405002-A1 COMBINATIONS OF DIACYLGLYCEROL ACYLTRANSFERASE 2 INHIBITORS AND ACETYL-COA CARBOXYLASE INHIBITOR ACAT2, ACACB, ACACA PDE4B 2308/4885SMN1; SMN2 4425/4885NPC1 162/4885
US-20210100798-A1 DIACYLGLYCEROL ACYL TRANSFERASE 2 INHIBITOR DGAT2, DGAT1, ACAT2 PDE4B 827/4885SMN1; SMN2 4814/4885NPC1 184/4885
US-20120202851-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE PIM1, PIM2, PIM3 PDE4B 1716/4885SMN1; SMN2 3818/4885NPC1 1582/4885
US-20120208815-A1 PIM KINASE INHIBITORS AND METHODS OF THEIR USE PIM1, PIM2, PIM3 PDE4B 2918/4885SMN1; SMN2 2557/4885NPC1 4325/4885
US-20110195956-A1 Heterocyclic Kinase Inhibitors PIM1, PIM2, PIM3 PDE4B 3388/4885SMN1; SMN2 1336/4885NPC1 4665/4885
US-11471458-B2 Diacylglycerol acyl transferase 2 inhibitor DGAT2, DGAT1, ACAT2 PDE4B 817/4885SMN1; SMN2 4817/4885NPC1 192/4885
US-20110195980-A1 Bicyclic Kinase Inhibitors PIM1, PIM2, PIM3 PDE4B 3668/4885SMN1; SMN2 1444/4885NPC1 4431/4885
US-20210100796-A1 DIACYLGLYCEROL ACYL TRANSFERASE 2 INHIBITOR DGAT2, DGAT1, ACAT2 PDE4B 817/4885SMN1; SMN2 4817/4885NPC1 192/4885

“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.