SCHEMBL571478

SCHEMBL571478

CC(C)OC(=O)C(O)C(O)C(=O)OC(C)C

nearest known ligand 0.50

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.50
HCAR2 Q8TDS4 1/20 0.39
TP53 P04637 1/20 0.35
CA12 O43570 6/20 0.35
CA1 P00915 6/20 0.35
CA2 P00918 6/20 0.35
CA9 Q16790 6/20 0.35
HTT P42858 1/20 0.35
CA7 P43166 3/20 0.34
CA14 Q9ULX7 3/20 0.34
LMNA P02545 3/20 0.34
ADRA1A P35348 1/20 0.33
PDE4D Q08499 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
KDM4E B2RXH2 1/20 0.32
USP2 O75604 1/20 0.32
ALDH1A1 P00352 1/20 0.32
HSD17B10 Q99714 1/20 0.32

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
SCHEMBL1338978 1.00 TSHR (0.50) TSHRHCAR2TP53CA12CA1
SCHEMBL1336756 1.00 TSHR (0.50) TSHRHCAR2TP53CA12CA1
SCHEMBL8636434 1.00 TSHR (0.50) TSHRHCAR2TP53CA12CA1
SCHEMBL5482220 0.89 TSHR (0.50) TSHRHCAR2TP53CA12CA1
SCHEMBL7438737 0.89 TSHR (0.42) TSHRHCAR2CA12CA1CA2
SCHEMBL12951517 0.88 TSHR (0.46) TSHRHCAR2TP53CA12CA1
SCHEMBL882439 0.88 TSHR (0.46) TSHRHCAR2TP53CA12CA1
SCHEMBL2246643 0.86 TSHR (0.43) TSHRHCAR2TP53CA12CA1
SCHEMBL2244398 0.86 TSHR (0.43) TSHRHCAR2TP53CA12CA1
SCHEMBL8272086 0.86 TSHR (0.43) TSHRHCAR2TP53CA12CA1

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 1333 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260144726-A1 POLYOL-FREE COSMETIC COMPOSITION COMPRISING ALPHA HYDROXY ACID ESTER L'OREAL (FR) 2026-05-28 US claimed
US-12252483-B2 Method for producing optically active 1, 4-benzothiazepine-1-oxide derivative AETAS PHARMA CO., LTD. (JP) 2025-03-18 US claimed
CN-119638969-A Degradable aromatic polyester polymer and synthesis method thereof 青岛大学 2025-03-18 CN claimed
CN-119104658-A Method for detecting valicarb-isopropyl tartrate genotoxic impurity D 山东百诺医药股份有限公司 2024-12-10 CN claimed
CN-119016001-A Micro-reaction system and method for synthesizing bio-based polyol 中建安装集团有限公司 2024-11-26 CN claimed
CN-115505108-B Hydrolysis-resistant titanium catalyst and preparation method and application thereof 中国石油化工股份有限公司 2024-08-30 CN claimed
CN-117603047-B Preparation method and application of bio-based polyol 中建安装集团有限公司 2024-06-11 CN claimed
US-11958818-B2 (R)-(2-methyloxiran-2-yl)methyl 4-bromobenzenesulfonate BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-04-16 US claimed
CN-117838769-A Combined suppository of valicarb-isopropyl tartrate and houttuynia cordata and preparation method thereof 湖北广济医药科技有限公司 2024-04-09 CN claimed
CN-115650787-B Liquid compositions containing urease inhibitors 甘肃云昊科技有限公司 2024-03-29 CN claimed
CN-1052668-A The compound of treatment inflammatory bowel disease LILLY CO ELI (US) 1991-07-03 CN claimed
EP-0434394-A2 Compounds for treating inflammatory bowel disease ELI LILLY AND COMPANY (US) 1991-06-26 EP claimed
EP-0417187-A1 RUTHENIUM-CATALYZED PRODUCTION OF CYCLIC SULFATES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1991-03-20 EP claimed
WO-1989011478-A1 RUTHENIUM-CATALYZED PRODUCTION OF CYCLIC SULFATES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1989-11-30 WO claimed
US-4764628-A Asymmetric epoxidation of allylic alcohols ARCO CHEMICAL COMPANY (US) 1988-08-16 US claimed
WO-1988001612-A1 PROCESSES AND INTERMEDIATES FOR N-(S-3-ALKYL-HEPTANOYL)-D-GAMMA-GLUTAMYL-GLYCYL-D-ALANINE PFIZER INC. (US) 1988-03-10 WO claimed
CN-87105898-A N-(sProcess and intermediates for the preparation of -3-alkylheptanoyl -D-r-glutamyl -glycyl -D-alanyl 1988-03-09 CN claimed
EP-0258032-A2 Processes and intermediates for N-(S-3-alkylheptanoyl)-D-gamma-glutamyl-glycyl-D-alanine PFIZER INC. (US) 1988-03-02 EP claimed
EP-0129044-A1 Synthesis of (+)-4-demethoxydaunomycinone THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 1984-12-27 EP claimed
US-4489206-A Synthesis of (+)-4-demethoxydaunomycinone ADRIA LABORATORIES, INC. (US) 1984-12-18 US claimed

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-12252483-B2 Method for producing optically active 1, 4-benzothiazepine-1-oxide derivative DUOX1, WNT1, CYP4Z1 TSHR 3929/4885HCAR2 2709/4885TP53 4529/4885
US-20260144726-A1 POLYOL-FREE COSMETIC COMPOSITION COMPRISING ALPHA HYDROXY ACID ESTER HAO2, HADH, LDHA TSHR 1891/4885HCAR2 11/4885TP53 598/4885
US-11958818-B2 (R)-(2-methyloxiran-2-yl)methyl 4-bromobenzenesulfonate CBR1, BRD4, DNMT1 TSHR 1940/4885HCAR2 2236/4885TP53 2291/4885

“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.