SCHEMBL247199

SCHEMBL247199

CC(C)(C)OC(=O)C[C@H]1C[C@@H](CO)OC(C)(C)O1

nearest known ligand 0.34

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
MIF P14174 1/20 0.34
NR1H2 P55055 1/20 0.34
HCRTR2 O43614 1/20 0.31
EPHX2 P34913 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
SCHEMBL9453175 1.00 MIF (0.34) MIFNR1H2HCRTR2EPHX2
SCHEMBL7720760 1.00 MIF (0.34) MIFNR1H2HCRTR2EPHX2
SCHEMBL5728730 1.00 MIF (0.34) MIFNR1H2HCRTR2EPHX2
Alcohol SCHEMBL6702863 0.97 MIF (0.33) MIFNR1H2
SCHEMBL31070837 0.88 MIF (0.33) MIFNR1H2
SCHEMBL15887309 0.88 MIF (0.33) MIFNR1H2
SCHEMBL4015355 0.88 MIF (0.33) MIFNR1H2
SCHEMBL22043547 0.88 CYP1A2 (0.39) MIFHCRTR2EPHX2
SCHEMBL6125270 0.88 MIF (0.34) MIFHCRTR2EPHX2
SCHEMBL4188806 0.87 MIF (0.34) MIFHCRTR2EPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109574939-B Preparation method of rosuvastatin sodium 安徽省庆云医药股份有限公司 2022-05-27 CN claimed
CN-109574999-B Preparation method of pitavastatin calcium intermediate 安徽省庆云医药股份有限公司 2022-03-08 CN claimed
EP-2526099-B1 IMPROVED PROCESS FOR THE PREPARATION OF AMIDE INTERMEDIATES AND THEIR USE THEREOF MSN LAB LTD (IN) 2016-03-30 EP claimed
US-20120323005-A1 Process For The Preparation Of Amide Intermediates And Their Use Thereof MSN LABORATORIES PRIVATE LIMITED (IN) 2012-12-20 US claimed
WO-2011086584-A2 IMPROVED PROCESS FOR THE PREPARATION OF AMIDE INTERMEDIATES AND THEIR USE THEREOF MSN LABORATORIES LIMITED (IN) 2011-07-21 WO claimed
EP-0577040-B1 Process for the preparation of (3R,5S)-6-hydroxy-3,5-O-isopropylidene-3,5-dihydroxy-hexanoic acid, tert.-butyl ester HOECHST AG (DE) 1997-09-24 EP claimed
EP-0577040-A2 Process for the preparation of (3R,5S)-6-hydroxy-3,5-O-isopropylidene-3,5-dihydroxy-hexanoic acid, tert.-butyl ester HOECHST AKTIENGESELLSCHAFT (DE) 1994-01-05 EP claimed
CN-115894431-B Preparation method of statin drug intermediate 南京欧信医药技术有限公司 2024-12-03 CN disclosed
CN-118561803-A Method for preparing rosuvastatin calcium intermediate by micro-channel reactor 江苏阿尔法集团盛基药业(宿迁)有限公司 2024-08-30 CN disclosed
CN-118515672-A Medicine with microcirculation improving effect and preparation method thereof 南京医科大学 2024-08-20 CN disclosed
US-11814355-B2 Method for synthesizing pitavastatin t-butyl ester ANHUI QINGYUN PHARMACEUTICAL AND CHEMICAL CO., LTD. (CN) 2023-11-14 US disclosed
US-11618731-B2 Prodrugs of kallikrein inhibitors BIOCRYST PHARMACEUTICALS, INC. (US) 2023-04-04 US disclosed
CN-115611848-A Synthetic method of rosuvastatin calcium intermediate 江苏阿尔法药业股份有限公司 2023-01-17 CN disclosed
EP-0577040-A2 Process for the preparation of (3R,5S)-6-hydroxy-3,5-O-isopropylidene-3,5-dihydroxy-hexanoic acid, tert.-butyl ester HOECHST AKTIENGESELLSCHAFT (DE) 1994-01-05 EP disclosed
EP-0577040-A2 Process for the preparation of (3R,5S)-6-hydroxy-3,5-O-isopropylidene-3,5-dihydroxy-hexanoic acid, tert.-butyl ester HOECHST AKTIENGESELLSCHAFT (DE) 1994-01-05 EP disclosed
US-5248793-A Process for the synthesis of (4R-cis)-1,1-dimethylethyl 6-iodomethyl or 6-(phenyl-substituted)sulfonyloxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate WARNER-LAMBERT COMPANY (US) 1993-09-28 US disclosed
EP-0553213-A1 PROCESS FOR THE SYNTHESIS OF (4R-CIS)-1,1-DIMETHYLETHYL-6-CYANOMETHYL-2,2-DIMETHYL-1,3-DIOXANE-4-ACETATE. WARNER LAMBERT CO (US) 1993-08-04 EP disclosed
WO-1992006968-A1 PROCESS FOR THE SYNTHESIS OF (4R-CIS)-1,1-DIMETHYLETHYL-6-CYANOMETHYL-2,2-DIMETHYL-1,3-DIOXANE-4-ACETATE WARNER-LAMBERT COMPANY (US) 1992-04-30 WO disclosed
US-5103024-A PROCESS FOR THE SYNTHESIS OF (4R-CIS)-1,1-DIMETHYLETHYL 6-CYANOMETHYL-2,2-DIMETHYL-1,3-DIOXANE-4-ACETATE WARNER-LAMBERT COMPANY (US) 1992-04-07 US disclosed
EP-0418648-A1 4-Hydroxytetrahydropyran-2-ones as well as the corresponding dehydroxy carbon acid derivatives, salts and esters, process for their preparation, pharmaceutical preparations as well as precursors HOECHST AKTIENGESELLSCHAFT (DE) 1991-03-27 EP 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 (3 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-11814355-B2 Method for synthesizing pitavastatin t-butyl ester SSTR4, DPP4, VIP MIF 1064/4885NR1H2 3671/4885HCRTR2 2131/4885
US-20120323005-A1 Process For The Preparation Of Amide Intermediates And Their Use Thereof CETP, LCAT, APOB MIF 4406/4885NR1H2 29/4885HCRTR2 3285/4885
US-11618731-B2 Prodrugs of kallikrein inhibitors KLKB1, SERPINB1, KLK1 MIF 2406/4885NR1H2 2376/4885HCRTR2 3262/4885

“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.