SCHEMBL7154526

SCHEMBL7154526

CO[C@H]1O[C@@H]2COC(c3ccccc3)O[C@H]2[C@H](OC(C)=O)[C@H]1OC(C)=O

nearest known ligand 0.67

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 3/20 0.67
▸ KMT2A Q03164 3/20 0.63
▸ MEN1 O00255 2/20 0.63
▸ ALDH1A1 P00352 4/20 0.43
▸ TSHR P16473 2/20 0.39
▸ MMP9 P14780 1/20 0.36
▸ MMP12 P39900 1/20 0.36
▸ PKM P14618 1/20 0.36
▸ BCHE P06276 1/20 0.34
▸ SELP P16109 1/20 0.34
▸ CYP3A4 P08684 1/20 0.33
▸ MAPT P10636 1/20 0.33
▸ CYP2C9 P11712 1/20 0.33
▸ SLC18A3 Q16572 1/20 0.33
▸ PTPN1 P18031 2/20 0.33
▸ LMNA P02545 1/20 0.33

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
SCHEMBL7155230 1.00 L3MBTL1 (0.67) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL7153425 1.00 L3MBTL1 (0.67) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL7145707 1.00 L3MBTL1 (0.67) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL7147270 1.00 L3MBTL1 (0.67) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL20109865 0.97 L3MBTL1 (0.69) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL25503290 0.93 L3MBTL1 (0.60) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL25503494 0.93 L3MBTL1 (0.60) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL25503299 0.93 L3MBTL1 (0.60) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL7563649 0.93 L3MBTL1 (0.60) L3MBTL1KMT2AMEN1ALDH1A1TSHR
SCHEMBL22073061 0.92 L3MBTL1 (0.66) L3MBTL1KMT2AMEN1ALDH1A1TSHR

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6562514-B1 Stabilized vanadium electrolyte solutions for all-vanadium redox cells and batteries PINNACLE VRB LIMITED (AU) 2003-05-13 — — US disclosed
US-6468688-B2 CHARGING, DISCHARGING EFFICIENCY; VANADIUM ELECTROLYTE PINNACLE VRB LIMITED (AU) 2002-10-22 — — US disclosed
US-20010028977-A1 Charging, discharging efficiency; vanadium electrolyte JD HOLDING INC. (KY) 2001-10-11 — — US disclosed
US-6043341-A PHOSPHONYLATING AGENTS FOR REGIOSELECTIVE AND REPRODUCIBLE CONVERSION OF PEPTIDES TO PHOSPHONIC ACID PRODRUGS ELI LILLY & CO. (US) 2000-03-28 — — US disclosed
EP-0906915-A1 Preparation of cyclic peptide antifungal agents ELI LILLY AND COMPANY (US) 1999-04-07 — — EP disclosed
EP-0829104-A1 HIGH ENERGY DENSITY VANADIUM ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND ALL-VANADIUM REDOX CELLS AND BATTERIES CONTAINING HIGH ENERGY VANADIUM ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1998-03-18 — — EP disclosed
EP-0729648-A4 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LTD (AU) 1997-01-02 — — EP disclosed
EP-0729648-A1 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1996-09-04 — — EP disclosed
WO-1995012219-A1 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1995-05-04 — — WO disclosed
US-4764605-A Process for selectively deacetylating acetyl derivatives of saccharides DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1988-08-16 — — US disclosed
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