SCHEMBL2997209

SCHEMBL2997209

CC(C)(C)OC(=O)Nc1ccc2c(c1)C(CO)c1ccccc1-2

nearest known ligand 0.49

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
EPHX2 P34913 1/20 0.46
IDO1 P14902 2/20 0.45
BRD4 O60885 2/20 0.43
CREBBP Q92793 2/20 0.43
CA12 O43570 1/20 0.43
CA1 P00915 1/20 0.43
CA9 Q16790 1/20 0.43
MDM2 Q00987 1/20 0.42
SLC10A2 Q12908 1/20 0.41
NR1I3 Q14994 3/20 0.40
ACSS2 Q9NR19 1/20 0.40
RORC P51449 3/20 0.39
CYP17A1 P05093 1/20 0.39

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
SCHEMBL1115135 0.94 CA12 (0.47) IDO1BRD4CREBBPCA12CA1
SCHEMBL12394690 0.87 MEN1 (0.41) EPHX2IDO1MDM2
SCHEMBL22664849 0.84 CA12 (0.45) EPHX2IDO1BRD4CREBBPCA12
SCHEMBL2465280 0.84 CA12 (0.45) IDO1BRD4CREBBPCA12CA1
SCHEMBL14062472 0.82 MAOA (0.54) EPHX2
SCHEMBL3006400 0.81 IDO1 (0.45) EPHX2IDO1BRD4CREBBPCA12
SCHEMBL14872697 0.80 CA12 (0.38) BRD4CREBBPCA12CA1CA9
SCHEMBL27810168 0.80 EPHX2 (0.60) EPHX2IDO1BRD4CREBBPMDM2
SCHEMBL12370472 0.80 EPHX2 (0.41) EPHX2
SCHEMBL13500221 0.80 RAB9A (0.58)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2714070-B1 LONG-ACTING GLP-1/GLUCAGON RECEPTOR AGONISTS OPKO BIOLOGICS LTD (IL) 2024-03-20 EP disclosed
EP-3924369-A1 LONG-ACTING GLP-2 ANALOGS OPKO Biologics Ltd. (IL) 2021-12-22 EP disclosed
CN-109096387-B Pegylated OXM variants 奥普科生物制品有限公司 2021-11-30 CN disclosed
CN-113710692-A Long-acting GLP-2 analogs OPKO生物科学有限公司 2021-11-26 CN disclosed
EP-3302571-B1 PEGYLATED OXYNTOMODULIN VARIANTS OPKO BIOLOGICS LTD (IL) 2020-11-18 EP disclosed
EP-3302571-B1 PEGYLATED OXYNTOMODULIN VARIANTS OPKO BIOLOGICS LTD (IL) 2020-11-18 EP disclosed
WO-2020165900-A1 LONG-ACTING GLP-2 ANALOGS OPKO BIOLOGICS LTD. (IL) 2020-08-20 WO disclosed
US-20200254065-A1 LONG-ACTING GLP-2 ANALOGS OPKO BIOLOGICS LTD. (IL) 2020-08-13 US disclosed
US-20200254065-A1 LONG-ACTING GLP-2 ANALOGS OPKO BIOLOGICS LTD. (IL) 2020-08-13 US disclosed
US-20190160152-A1 LONG-ACTING OXYNTOMODULIN FORMULATION AND METHODS OF PRODUCING AND ADMINISTERING SAME OPKO BIOLOGICS LTD. (IL) 2019-05-30 US disclosed
WO-2010014258-A2 CONJUGATES HAVING A RELEASABLE LINKAGE NEKTAR THERAPEUTICS AL, CORPORATION (US) 2010-02-04 WO disclosed
US-7585837-B2 derivatization of the drug with 9-fluorenylmethoxycarbonyl (Fmoc) or 2-sulfo-9-fluorenylmethoxycarbonyl (FMS) removable under mild basic conditions by attaching a protein or polymer carrier to derivatized drug molecule,such carrier serving for delivery of the drug YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2009-09-08 US disclosed
US-7585837-B2 derivatization of the drug with 9-fluorenylmethoxycarbonyl (Fmoc) or 2-sulfo-9-fluorenylmethoxycarbonyl (FMS) removable under mild basic conditions by attaching a protein or polymer carrier to derivatized drug molecule,such carrier serving for delivery of the drug YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2009-09-08 US disclosed
US-7585837-B2 derivatization of the drug with 9-fluorenylmethoxycarbonyl (Fmoc) or 2-sulfo-9-fluorenylmethoxycarbonyl (FMS) removable under mild basic conditions by attaching a protein or polymer carrier to derivatized drug molecule,such carrier serving for delivery of the drug YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2009-09-08 US disclosed
US-20090005574-A1 reacting a 9-hydroxymethyl-2-amino fluorene with a silyl protecting reagent e.g. tert-butyldimethylsilyl chloride to form tert-butyldimethylsiloxy-9-methyl-2-aminofluorene, reacting intermediate with 3-maleimidopropionic acid; protecting; chemical intermediates for protein and peptide drugs BAXTER INTERNATIONAL INC. (US) 2009-01-01 US disclosed
US-20090005574-A1 reacting a 9-hydroxymethyl-2-amino fluorene with a silyl protecting reagent e.g. tert-butyldimethylsilyl chloride to form tert-butyldimethylsiloxy-9-methyl-2-aminofluorene, reacting intermediate with 3-maleimidopropionic acid; protecting; chemical intermediates for protein and peptide drugs BAXTER INTERNATIONAL INC. (US) 2009-01-01 US disclosed
US-20090005574-A1 reacting a 9-hydroxymethyl-2-amino fluorene with a silyl protecting reagent e.g. tert-butyldimethylsilyl chloride to form tert-butyldimethylsiloxy-9-methyl-2-aminofluorene, reacting intermediate with 3-maleimidopropionic acid; protecting; chemical intermediates for protein and peptide drugs BAXTER INTERNATIONAL INC. (US) 2009-01-01 US disclosed
WO-2009000523-A1 METHOD FOR PREPARING FMOC-BASED HYDROLYSABLE LINKERS BAXTER INTERNATIONAL INC. (US) 2008-12-31 WO disclosed
WO-2009000523-A1 METHOD FOR PREPARING FMOC-BASED HYDROLYSABLE LINKERS BAXTER INTERNATIONAL INC. (US) 2008-12-31 WO disclosed
US-20060171920-A1 derivatization of the drug with 9-fluorenylmethoxycarbonyl (Fmoc) or 2-sulfo-9-fluorenylmethoxycarbonyl (FMS) removable under mild basic conditions by attaching a protein or polymer carrier to derivatized drug molecule,such carrier serving for delivery of the drug YEDA RESEARCH AND DEVELOPMENT CO., LTD. (IL) 2006-08-03 US 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 (4 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-20060171920-A1 derivatization of the drug with 9-fluorenylmethoxycarbonyl (Fmoc) or 2-sulfo-9-fluorenylmethoxycarbonyl (FMS) removable under mild basic conditions by attaching a protein or polymer carrier to derivatized drug molecule,such carrier serving for delivery of the drug PTMS, FIBP, FLT3 EPHX2 2383/4885IDO1 4610/4885BRD4 604/4885
US-20090005574-A1 reacting a 9-hydroxymethyl-2-amino fluorene with a silyl protecting reagent e.g. tert-butyldimethylsilyl chloride to form tert-butyldimethylsiloxy-9-methyl-2-aminofluorene, reacting intermediate with 3-maleimidopropionic acid; protecting; chemical intermediates for protein and peptide drugs HGFAC, PTMS, PRMT9 EPHX2 3437/4885IDO1 4529/4885BRD4 1194/4885
US-20200254065-A1 LONG-ACTING GLP-2 ANALOGS GLP1R, GIPR, GCGR EPHX2 2386/4885IDO1 4327/4885BRD4 2240/4885
US-20190160152-A1 LONG-ACTING OXYNTOMODULIN FORMULATION AND METHODS OF PRODUCING AND ADMINISTERING SAME OGFR, VEGFA, OGFRL1 EPHX2 1338/4885IDO1 4374/4885BRD4 4681/4885

“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.