SCHEMBL15908130

SCHEMBL15908130

CN1CCN(C(=O)OCCOCCOCCO)CC1

nearest known ligand 0.39

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
SMN1; SMN2 Q16637 3/20 0.39
ALDH1A1 P00352 3/20 0.39
POLB P06746 2/20 0.39
HTT P42858 1/20 0.39
LMNA P02545 2/20 0.38
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
HTR1A P08908 1/20 0.37
RECQL P46063 1/20 0.37
TSHR P16473 1/20 0.36
KDM4E B2RXH2 2/20 0.36
APP P05067 1/20 0.35
HSD17B10 Q99714 1/20 0.35
GAA P10253 1/20 0.35
ATM Q13315 1/20 0.35

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
SCHEMBL29316060 0.89 POLB (0.42) CYP1A2TDP1SMN1; SMN2ALDH1A1POLB
SCHEMBL15934091 0.86 KDM4E (0.44) CYP1A2TDP1SMN1; SMN2ALDH1A1POLB
SCHEMBL25980626 0.83 MEN1 (0.38) TDP1SMN1; SMN2ALDH1A1POLBHTT
SCHEMBL25588991 0.82 ALDH1A1 (0.37) SMN1; SMN2ALDH1A1POLBHTTLMNA
SCHEMBL20436763 0.82 ALDH1A1 (0.37) SMN1; SMN2ALDH1A1POLBHTTLMNA
SCHEMBL19661315 0.82 HTR1A (0.38) CYP1A2TDP1SMN1; SMN2ALDH1A1POLB
SCHEMBL15934092 0.80 KDM4E (0.47) CYP1A2TDP1SMN1; SMN2ALDH1A1POLB
SCHEMBL15934122 0.80 TDP1 (0.43) CYP1A2TDP1SMN1; SMN2ALDH1A1POLB
SCHEMBL20464009 0.80 MEN1 (0.35) SMN1; SMN2ALDH1A1POLBHTTLMNA
SCHEMBL14415917 0.79 KMT2A (0.38) TDP1SMN1; SMN2ALDH1A1POLBLMNA

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
US-20230038956-A1 METHODS FOR TREATING MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2023-02-09 US disclosed
EP-3554554-B1 EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS INC (US) 2022-09-07 EP disclosed
US-11382981-B2 Exon skipping oligomer conjugates for muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2022-07-12 US disclosed
US-10947533-B2 Processes for preparing phosphorodiamidate morpholino oligomers SAREPTA THERAPEUTICS, INC. (US) 2021-03-16 US disclosed
US-10888578-B2 Exon skipping oligomer conjugates for muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2021-01-12 US disclosed
WO-2020023688-A1 EXON SKIPPING OLIGOMERS FOR MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2020-01-30 WO disclosed
US-20140213737-A1 ANTIBACTERIAL ANTISENSE OLIGONUCLEOTIDE AND METHOD SAREPTA THERAPEUTICS, INC. (US) 2014-07-31 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 (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-20230038956-A1 METHODS FOR TREATING MUSCULAR DYSTROPHY UTRN, MTPN, SMN1; SMN2 CYP1A2 4465/4885TDP1 101/4885SMN1; SMN2 3/4885
US-11382981-B2 Exon skipping oligomer conjugates for muscular dystrophy UTRN, SMN1; SMN2, RBM17 CYP1A2 4832/4885TDP1 757/4885SMN1; SMN2 2/4885
US-10888578-B2 Exon skipping oligomer conjugates for muscular dystrophy UTRN, SMN1; SMN2, DCLRE1B CYP1A2 4836/4885TDP1 755/4885SMN1; SMN2 2/4885
US-20140213737-A1 ANTIBACTERIAL ANTISENSE OLIGONUCLEOTIDE AND METHOD RNGTT, SPOUT1, MRPL21 CYP1A2 4831/4885TDP1 754/4885SMN1; SMN2 668/4885

“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.