SCHEMBL17258352

SCHEMBL17258352

CCOCNCCOCCOCC(=O)O

nearest known ligand 0.37

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
EPHX2 P34913 1/20 0.37
ALDH1A1 P00352 2/20 0.34
TSHR P16473 1/20 0.34
THRB P10828 1/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
KDM4E B2RXH2 3/20 0.34
LMNA P02545 1/20 0.34
GLP1R P43220 8/20 0.33
CYP2C19 P33261 1/20 0.33
SMN1; SMN2 Q16637 2/20 0.32
RECQL P46063 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
SCHEMBL26129806 0.89 ALDH1A1 (0.41) EPHX2ALDH1A1TSHRTHRBMEN1
SCHEMBL6317524 0.84 KDM4E (0.35) EPHX2ALDH1A1MEN1KMT2AKDM4E
SCHEMBL7268276 0.82 SMN1; SMN2 (0.38) EPHX2ALDH1A1TSHRTHRBMEN1
SCHEMBL27386798 0.82 SMN1; SMN2 (0.38) EPHX2ALDH1A1TSHRTHRBMEN1
SCHEMBL30971878 0.81 EPHX2 (0.42) EPHX2ALDH1A1TSHRMEN1KMT2A
SCHEMBL18251468 0.81 EPHX2 (0.42) EPHX2ALDH1A1TSHRMEN1KMT2A
SCHEMBL16538964 0.81 EPHX2 (0.34) EPHX2ALDH1A1MEN1KMT2AKDM4E
SCHEMBL2865428 0.80 ALDH1A1 (0.50) EPHX2ALDH1A1TSHRTHRBCYP2C19
SCHEMBL22609510 0.80 ALDH1A1 (0.50) EPHX2ALDH1A1TSHRTHRBCYP2C19
SCHEMBL6275021 0.80 ALDH1A1 (0.50) EPHX2ALDH1A1TSHRTHRBCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114901673-B Preparation method of solution phase peptide nucleic acid oligomer 海阳生物材料有限公司 2025-02-18 CN disclosed
US-20230108350-A1 METHOD FOR PRODUCING PNA OLIGOMER IN SOLUTION PROCESS SEASUNBIO MATERIALS (KP) 2023-04-06 US disclosed
EP-4083054-A1 METHOD FOR PRODUCING PNA OLIGOMER IN SOLUTION PROCESS Seasunbio Materials (KR) 2022-11-02 EP disclosed
CN-114901673-A Method for preparing solution phase peptide nucleic acid oligomer 海阳生物材料有限公司 2022-08-12 CN disclosed
WO-2021133033-A1 METHOD FOR PRODUCING PNA OLIGOMER IN SOLUTION PROCESS 주식회사 시선바이오머티리얼스 2021-07-01 WO disclosed
US-9469656-B2 HDAC inhibitors as anti-cancer agents THE UNIVERSITY OF TOLEDO (US) 2016-10-18 US disclosed
US-20150329560-A1 HDAC Inhibitors as Anti-Cancer Agents THE UNIVERSITY OF TOLEDO (US) 2015-11-19 US 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 (2 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-20230108350-A1 METHOD FOR PRODUCING PNA OLIGOMER IN SOLUTION PROCESS NCL, POLI, RNGTT EPHX2 2415/4885ALDH1A1 4771/4885TSHR 2920/4885
US-20150329560-A1 HDAC Inhibitors as Anti-Cancer Agents HDAC1, HDAC4, HDAC5 EPHX2 2766/4885ALDH1A1 1221/4885TSHR 4383/4885

“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.