SCHEMBL23913857

SCHEMBL23913857

COc1cc(C(=O)OCC(=O)O)cc(OC)c1OC

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.62
TSHR P16473 3/20 0.59
USP2 O75604 1/20 0.59
L3MBTL1 Q9Y468 2/20 0.59
MAPK1 P28482 2/20 0.59
KMT2A Q03164 4/20 0.58
SLC29A1 Q99808 3/20 0.57
KDM4E B2RXH2 1/20 0.57
PKM P14618 1/20 0.57
NPSR1 Q6W5P4 1/20 0.56
SCN1A P35498 1/20 0.56
SCN2A Q99250 1/20 0.56
SCN3A Q9NY46 1/20 0.56
TDP1 Q9NUW8 1/20 0.56
POLB P06746 2/20 0.54
CYP3A4 P08684 2/20 0.54
CYP2C9 P11712 1/20 0.54
ALDH1A1 P00352 1/20 0.54
MAPT P10636 2/20 0.53
RAB9A P51151 1/20 0.53

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
Ethyltrimethoxy Benzoate SCHEMBL4410910 0.82 KMT2A (0.66) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL18675989 0.81 SCN1A (0.66) SMN1; SMN2TSHRMAPK1KMT2ASLC29A1
SCHEMBL10887449 0.81 SLC29A1 (0.59) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL7952964 0.81 SLC29A1 (0.59) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL10428390 0.81 SLC29A1 (0.59) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL10428055 0.81 SLC29A1 (0.59) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL23913855 0.80 SMN1; SMN2 (0.56) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL2612570 0.79 SLC29A1 (0.57) SMN1; SMN2TSHRUSP2L3MBTL1MAPK1
SCHEMBL9680396 0.79 SLC29A1 (0.66) SMN1; SMN2TSHRUSP2MAPK1KMT2A
SCHEMBL19900752 0.79 HSD17B2 (0.72) SMN1; SMN2TSHRKMT2AKDM4ETDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240239834-A1 ALKOXYPHENYL DERIVATIVES, PROTECTED NUCLEOSIDES AND PROTECTED NUCLEOTIDES, METHOD FOR PRODUCING OLIGONUCLEOTIDES, AND METHOD FOR REMOVING SUBSTITUENTS FUJIMOTO CHEMICALS CO., LTD., (JP) 2024-07-18 US disclosed
US-20240239833-A1 ALKOXYPHENYL DERIVATIVES, PROTECTED NUCLEOSIDES AND PROTECTED NUCLEOTIDES, METHOD FOR PRODUCING OLIGONUCLEOTIDES, AND METHOD FOR REMOVING SUBSTITUENTS FUJIMOTO CHEMICALS CO., LTD., (JP) 2024-07-18 US disclosed
US-20210317159-A1 ALKOXYPHENYL DERIVATIVES, PROTECTED NUCLEOSIDES AND PROTECTED NUCLEOTIDES, METHOD FOR PRODUCING OLIGONUCLEOTIDES, AND METHOD FOR REMOVING SUBSTITUENTS FUJIMOTO CHEMICALS CO., LTD. (JP) 2021-10-14 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 (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-20240239834-A1 ALKOXYPHENYL DERIVATIVES, PROTECTED NUCLEOSIDES AND PROTECTED NUCLEOTIDES, METHOD FOR PRODUCING OLIGONUCLEOTIDES, AND METHOD FOR REMOVING SUBSTITUENTS ROS1, POLN, RNMT SMN1; SMN2 232/4885TSHR 3184/4885USP2 4511/4885
US-20210317159-A1 ALKOXYPHENYL DERIVATIVES, PROTECTED NUCLEOSIDES AND PROTECTED NUCLEOTIDES, METHOD FOR PRODUCING OLIGONUCLEOTIDES, AND METHOD FOR REMOVING SUBSTITUENTS ROS1, POLN, RNMT SMN1; SMN2 232/4885TSHR 3184/4885USP2 4511/4885
US-20240239833-A1 ALKOXYPHENYL DERIVATIVES, PROTECTED NUCLEOSIDES AND PROTECTED NUCLEOTIDES, METHOD FOR PRODUCING OLIGONUCLEOTIDES, AND METHOD FOR REMOVING SUBSTITUENTS ROS1, POLN, RNMT SMN1; SMN2 232/4885TSHR 3184/4885USP2 4511/4885

“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.