SCHEMBL3369453

SCHEMBL3369453

O=C(O)C(CO)C1COCCO1

nearest known ligand 0.46

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.34
HTT P42858 1/20 0.34
KMT2A Q03164 1/20 0.34

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
SCHEMBL3867748 0.84 CHRM2 (0.31) MEN1HTTKMT2A
SCHEMBL11451574 0.79 MEN1 (0.45) MEN1HTTKMT2A
SCHEMBL31457109 0.78 FOLH1 (0.33)
SCHEMBL28093354 0.76
SCHEMBL12497665 0.76 MEN1 (0.54) MEN1HTTKMT2A
SCHEMBL15971664 0.75 IDUA (0.32)
SCHEMBL4716948 0.74 CHRM2 (0.32)
SCHEMBL21751551 0.73 KDM4E (0.40) MEN1KMT2A
SCHEMBL31727940 0.71 CHRM2 (0.34)
SCHEMBL21751634 0.71 CHRM2 (0.31)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0349469-A1 Pharmaceutical product having skin regenerating properties based on the active principle of mimosa tenuiflora, and process for producing same Tellez Perez, Julio (MX) 1990-01-03 EP claimed
EP-1619191-B1 Process for producing optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4-yl] acetic acid derivatives KANEKA CORP (JP) 2010-10-27 EP disclosed
EP-1394157-B1 Process for the preparation of 3,5-dihydroxy substituted esters as intermediates for producing optically active 2-(6-(hydroxymethyl)-1,3-dioxan-4-yl) acetic acid dervatives KANEKA CORP (JP) 2007-10-17 EP disclosed
EP-1288213-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2- 6-(HYDROXY-METHYL)-1,3-DIOXAN-4-YL|ACETIC ACID DERIVATIVES KANEKA CORP (JP) 2006-11-29 EP disclosed
US-20060246557-A1 Process for preparing optically active 2-[6-(hydroxy-methyl)-1,3-dioxan-4-yl] acetic acid derivatives KANEKA CORPORATION (JP) 2006-11-02 US disclosed
US-7094594-B2 Process for preparing optically active 2-[6-(hydroxy-methyl)-1,3-dioxan-4-yl] acetic acid derivatives KANEKA CORPORATION (JP) 2006-08-22 US disclosed
EP-1619191-A2 Process for producing optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4-yl] acetic acid derivatives KANEKA CORPORATION (JP) 2006-01-25 EP disclosed
US-6903225-B2 Process for producing optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4-yl]acetic acid derivatives KANEKA CORPORATION (JP) 2005-06-07 US disclosed
US-20050080277-A1 Process for preparing optically active 2-[6-(hydroxy-methyl)-1,3-dioxan-4-yl] acetic acid derivatives KANEKA CORPORATION (JP) 2005-04-14 US disclosed
EP-1024139-B1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE 2-(6-(HYDROXYMETHYL)-1,3-DIOXAN-4-YL) ACETIC ACID DERIVATIVES KANEKA CORP (JP) 2004-05-12 EP disclosed
EP-1288213-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2- 6-(HYDROXY-METHYL)-1,3-DIOXAN-4-YL]ACETIC ACID DERIVATIVES KANEKA CORPORATION (JP) 2003-03-05 EP disclosed
US-20030040634-A1 Process for producing optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4yl]acetic acid derivatives KANEKA CORPORATION (JP) 2003-02-27 US disclosed
US-6472544-B1 REACTING ACETIC ACID DERIVATIVE WITH AN ENOLATE, REDUCING WITH A MICROORGANISM, ACETALIZING IN PRESENCE OF ACID CATALYST THEN ALKALINE SAPONIFICATION; NO SPECIAL EQUIPMENT OR SUPER LOW TEMPERATURE REQUIRED; INEXPENSIVE STARTING MATERIALS KANEKA CORPORATION (JP) 2002-10-29 US disclosed
US-20010041796-A1 Pentacyclic compound TERASAWA HIROFUMI (JP) 2001-11-15 US disclosed
EP-0826688-B1 PENTACYCLIC COMPOUNDS DAIICHI SEIYAKU CO (JP) 2001-09-05 EP disclosed
US-6211363-B1 TAXANE COMPOUNDS; ANTITUMOR AGENTS DAIICHI PHARAMACEUTICAL CO., LTD. (JP) 2001-04-03 US disclosed
EP-1024139-A1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE 2- 6-(HYDROXYMETHYL)-1,3-DIOXAN-4-YL]ACETIC ACID DERIVATIVES KANEKA CORPORATION (JP) 2000-08-02 EP disclosed
US-6075140-A A TAXOL DERIVATIVE CONTAINING PENTACYCLIC RING IN WHICH 9 AND 10 POSITION HYDROXYL GROUP ARE CHANGED TO CYCLIC ACETAL GROUP IS USEFUL AS ANTITUMOR AGENT DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2000-06-13 US disclosed
EP-0826688-A1 PENTACYCLIC COMPOUNDS DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1998-03-04 EP disclosed
EP-0349469-A1 Pharmaceutical product having skin regenerating properties based on the active principle of mimosa tenuiflora, and process for producing same Tellez Perez, Julio (MX) 1990-01-03 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 (4 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-20030040634-A1 Process for producing optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4yl]acetic acid derivatives HAAO, APEH, AADAC MEN1 2905/4885HTT 1256/4885KMT2A 627/4885
US-20010041796-A1 Pentacyclic compound RPL31, BCOR, OXER1 MEN1 3289/4885HTT 4326/4885KMT2A 2812/4885
US-20060246557-A1 Process for preparing optically active 2-[6-(hydroxy-methyl)-1,3-dioxan-4-yl] acetic acid derivatives HAAO, APEH, HPD MEN1 1586/4885HTT 1172/4885KMT2A 1181/4885
US-20050080277-A1 Process for preparing optically active 2-[6-(hydroxy-methyl)-1,3-dioxan-4-yl] acetic acid derivatives HAAO, APEH, HPD MEN1 2042/4885HTT 1354/4885KMT2A 1397/4885

“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.