Demannose

Demannose

SCHEMBL344073

CC(C)=O.CC(C)=O.O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
TDP1 Q9NUW8 1/20 0.46
PDE4A P27815 1/20 0.45
USP2 O75604 1/20 0.42
SLCO1B1 Q9Y6L6 1/20 0.42
KDM4E B2RXH2 2/20 0.40
AKR1B1 P15121 1/20 0.37
TOP1 P11387 1/20 0.33
PAX8 Q06710 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.32
MPI P34949 1/20 0.31
CYP2C19 P33261 1/20 0.30
HIF1A Q16665 1/20 0.30

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
Galactose SCHEMBL7892167 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL9123753 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL9468628 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL9453431 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL8340896 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL23929880 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Galactose SCHEMBL7895408 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL2317892 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL8213035 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2
Demannose SCHEMBL28123189 1.00 LMNA (0.48) LMNAL3MBTL1TDP1PDE4AUSP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119823200-A Preparation method of fondaparinux sodium heparin pentasaccharide and method for synthesizing fondaparinux sodium heparin pentasaccharide by taking naphthylmethyl as temporary protecting group 海南大学 2025-04-15 CN claimed
CN-119707372-A Low-shrinkage high-crack-resistance concrete and application thereof 中交第四航务工程局有限公司 2025-03-28 CN claimed
CN-118955585-A Preparation method of D-mannosamine and N-substituted derivative thereof 中国科学院深圳先进技术研究院 2024-11-15 CN claimed
CN-118359593-A Synthesis method of multi-chiral delta-lactone compound 北京化工大学 2024-07-19 CN claimed
CN-117510558-A Preparation method of marine machinery antirust agent 范斌磊 2024-02-06 CN claimed
CN-117384177-A Synthesis method of chiral pyrrole bridged ring compound 北京化工大学 2024-01-12 CN claimed
CN-117105994-A Synthesis method of 3' -O-methoxy guanosine 天津全和诚科技有限责任公司 2023-11-24 CN claimed
CN-117003604-A Synthesis method and flow of allyl fluoroalkyl compound 武汉大学 2023-11-07 CN claimed
CN-114146719-B Carbon plate-non-split-phase boron carbon nitrogen in-plane heterostructure and preparation method thereof 武汉科技大学 2023-10-24 CN claimed
CN-116425813-A Method for stereoselectively synthesizing beta-oxo-glycoside from 3-O-quinaldinate allyl sugar donor 三峡大学 2023-07-14 CN claimed
JP-3043813-B2 2000-05-22 JP claimed
US-5840921-A Method for the preparation of aldol product 7B SARAWAK MEDICHEM PHARMACEUTICALS, INC. (US) 1998-11-24 US claimed
US-5789599-A Aziridine compounds, methods of preparation and reactions thereof DREXEL UNIVERSITY (US) 1998-08-04 US claimed
US-5637683-A REACTING AN AMINE HAVING BASE SELECTED FROM URACIL, ADENINE, GUANINE, CYTOSINE, THYMINE, OR HYPOXANTHINE, WITH PENTAFLUOROPHENYL ESTER DERIVATIVE TO FORM INTERMEDIATE, REACTING INTERMEDIATE WITH ADDITIONAL AMINE CORNELL RESEARCH FOUNDATION, INC. (US) 1997-06-10 US claimed
EP-0775130-A1 METHOD FOR THE PREPARATION OF (+/-)-CALANOLIDE A AND INTERMEDIATES THEREOF MEDICHEM RESEARCH, INC. (US) 1997-05-28 EP claimed
WO-1996021507-A1 CATALYST FOR ASYMMETRIC DIELS-ALDER REACTIONS ALBEMARLE CORPORATION (US) 1996-07-18 WO claimed
WO-1996004263-A1 METHOD FOR THE PREPARATION OF (±)-CALANOLIDE A AND INTERMEDIATES THEREOF MEDICHEM RESEARCH, INC. (US) 1996-02-15 WO claimed
WO-1995030672-A1 AZIRIDINE COMPOUNDS, METHODS OF PREPARATION AND REACTIONS THEREOF DREXEL UNIVERSITY (US) 1995-11-16 WO claimed
EP-0520654-A1 Deep UV light sensitive positive photoresist compositions HOECHST CELANESE CORPORATION (US) 1992-12-30 EP claimed
EP-0113561-A2 Prostaglandin intermediates, their synthesis and their conversion to prostaglandins THE UPJOHN COMPANY (US) 1984-07-18 EP claimed