SCHEMBL4971166

SCHEMBL4971166

CCOC(=O)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C

nearest known ligand 0.83

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 2/20 0.83
▸ MEN1 O00255 2/20 0.83
▸ KMT2A Q03164 2/20 0.83
▸ USP2 O75604 2/20 0.83
▸ MAPK1 P28482 2/20 0.83
▸ LMNA P02545 1/20 0.83
▸ GPBAR1 Q8TDU6 10/20 0.78
▸ SLC10A2 Q12908 2/20 0.78
▸ TBXA2R P21731 1/20 0.78
▸ PDE3A Q14432 1/20 0.78
▸ NR1H4 Q96RI1 1/20 0.78
▸ CA1 P00915 3/20 0.69
▸ CA2 P00918 3/20 0.69
▸ ABCC4 O15439 1/20 0.65
▸ CYP2C9 P11712 1/20 0.65
▸ HIF1A Q16665 1/20 0.65
▸ VDR P11473 1/20 0.65
▸ CYP3A4 P08684 2/20 0.62
▸ SLCO1B3 Q9NPD5 1/20 0.62
▸ SLCO1B1 Q9Y6L6 1/20 0.62

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
SCHEMBL22699678 1.00 MAPT (0.83) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL5430802 0.96 MAPT (0.77) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL18216458 0.94 MAPT (0.81) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL26425523 0.93 MAPT (0.80) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL5436906 0.93 MAPT (0.80) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL137537 0.92 MAPT (0.76) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL23710355 0.92 MAPT (0.81) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL5431048 0.92 MAPT (0.81) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL1014063 0.92 MAPT (0.81) MAPTMEN1KMT2AUSP2MAPK1
SCHEMBL2260486 0.92 MAPT (0.81) MAPTMEN1KMT2AUSP2MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117964808-A Solid catalyst component, preparation method, catalyst system and application 中国石油化工股份有限公司 2024-05-03 — — CN claimed
CN-117964807-A Solid catalyst component for olefin polymerization, preparation method, catalyst system and application 中国石油化工股份有限公司 2024-05-03 — — CN claimed
CN-117964808-A Solid catalyst component, preparation method, catalyst system and application 中国石油化工股份有限公司 2024-05-03 — — CN disclosed
CN-117964807-A Solid catalyst component for olefin polymerization, preparation method, catalyst system and application 中国石油化工股份有限公司 2024-05-03 — — CN disclosed
US-10858387-B2 Process for the preparation of deoxycholic acid GLENMARK LIFE SCIENCES LIMITED (IN) 2020-12-08 — — US disclosed
US-20200140478-A1 PROCESS FOR THE PREPARATION OF DEOXYCHOLIC ACID GLENMARK PHARMACEUTICALS LIMITED (IN) 2020-05-07 — — US disclosed
EP-1968612-A2 NUCLEOTIDE AND OLIGONUCLEOTIDE PRODRUGS SPRING BANK (US) 2008-09-17 — — EP disclosed
US-20070254247-A1 Radiation-sensitive resin composition YAMAMOTO MASAFUMI 2007-11-01 — — US disclosed
WO-2007070598-A2 NUCLEOTIDE AND OLIGONUCLEOTIDE PRODRUGS SPRING BANK (US) 2007-06-21 — — WO disclosed
CN-1266192-C Diamine compound, polyamic acid, imidized polymer, liquid crystal aligning agent and liquid crystal display element JSR CO LTD (JP) 2006-07-26 — — CN disclosed
US-7008900-B1 Double metal cyanide catalysts for producing polyether polyols BAYER AKTIENGESELLSCHAFT (DE) 2006-03-07 — — US disclosed
CN-1564840-A Diamine compound, polyamic acid, imide polymer, liquid crystal alignment agent and liquid crystal display JSR CO LTD (JP) 2005-01-12 — — CN disclosed
US-6833431-B2 Polymerization catalyst containing one double-metal cyanide compound; an organic complexing ligand which is not a polyether, or a bile acid, a bile ester, bile salt or bile amide; a polyether and a bile acid or salt BAYER AKTIENGESELLSCHAFT (DE) 2004-12-21 — — US disclosed
US-6800419-B2 FOR USE AS CHEMICALLY-AMPLIFIED RESIST FOR MICROFABRICATION UTILIZING DEEP ULTRAVIOLET RAYS AND EXHIBITS EXCELLENT FILM THICKNESS UNIFORMITY AND STORAGE STABILITY JSR CORPORATION (JP) 2004-10-05 — — US disclosed
US-20040146802-A1 Radiation-sensitive resin composition JSR CORPORATION (JP) 2004-07-29 — — US disclosed
CN-1144616-C Double metal cyanide catalysts for preparing polyether polyols — 2004-04-07 — — CN disclosed
US-20030203307-A1 Radiation-sensitive resin composition JSR CORPORATION (JP) 2003-10-30 — — US disclosed
US-20030204045-A1 Double-metal cyanide catalysts for preparing polyether polyols BAYER AKTIENGESELLSCHAFT (DE) 2003-10-30 — — US disclosed
US-20020198099-A1 Double metal cyanide catalysts for preparing polyether polyols BAYER AKTIENGESELLSCHAFT (DE) 2002-12-26 — — US disclosed
CN-1387460-A Double metal cyanide catalysts for preparing polyether polyols BAYER AG (DE) 2002-12-25 — — CN 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-20200140478-A1 PROCESS FOR THE PREPARATION OF DEOXYCHOLIC ACID DHCR7, NR1H4, CYP46A1 MAPT 4340/4885MEN1 2116/4885KMT2A 3931/4885
US-10858387-B2 Process for the preparation of deoxycholic acid DHCR7, NR1H4, CYP46A1 MAPT 4340/4885MEN1 2116/4885KMT2A 3931/4885

“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.

Send feedback