SCHEMBL14415917

SCHEMBL14415917

O=C(OCCOCCOCCO)N1CCNCC1

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.38
MEN1 O00255 2/20 0.38
CA2 P00918 2/20 0.37
CA12 O43570 1/20 0.37
CA1 P00915 1/20 0.37
CA9 Q16790 1/20 0.37
CHKA P35790 1/20 0.36
TPSAB1 Q15661 1/20 0.36
TPSD1 Q9BZJ3 1/20 0.36
TPSG1 Q9NRR2 1/20 0.36
CHRNB2 P17787 1/20 0.35
CHRNA3 P32297 1/20 0.35
CHRNA4 P43681 1/20 0.35
CHRNB3 Q05901 1/20 0.35
CHRNA6 Q15825 1/20 0.35
POLB P06746 2/20 0.35
LMNA P02545 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
TSHR P16473 2/20 0.34
MAPK1 P28482 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
SCHEMBL22122716 0.89 CA2 (0.42) KMT2ACA2CA12CA1CA9
SCHEMBL22672640 0.85 MEN1 (0.40) KMT2AMEN1CA2CA12CA1
SCHEMBL22838001 0.85 ALDH1A1 (0.44) KMT2AMEN1CA2CA12CA1
SCHEMBL23094386 0.85 POLB (0.44) KMT2AMEN1CA2CA12CA1
SCHEMBL22672756 0.85 CA2 (0.36) KMT2AMEN1CA2CA12CA1
SCHEMBL28275432 0.82 POLB (0.44) KMT2ACA2CA12CA1CA9
SCHEMBL22115271 0.82 CA2 (0.34) KMT2AMEN1CA2CA12CA1
SCHEMBL24234390 0.82 POLB (0.36) KMT2AMEN1CA2CA12CA1
SCHEMBL20844330 0.81 SMN1; SMN2 (0.38) KMT2AMEN1CA2CA12CA1
SCHEMBL15908130 0.79 CYP1A2 (0.39) KMT2AMEN1POLBLMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230193282-A1 TREATMENT METHODS FOR MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2023-06-22 US disclosed
US-11642364-B2 Exon skipping oligomer conjugates for muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2023-05-09 US disclosed
US-20230045831-A1 PROCESSES FOR PREPARING PHOSPHORODIAMIDATE MORPHOLINO OLIGOMERS SAREPTA THERAPEUTICS, INC. (US) 2023-02-16 US disclosed
US-20230038956-A1 METHODS FOR TREATING MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2023-02-09 US disclosed
US-20220403385-A1 COMPOSITIONS FOR TREATING MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2022-12-22 US disclosed
US-11491238-B2 Exon skipping oligomer conjugates for muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2022-11-08 US disclosed
US-11382981-B2 Exon skipping oligomer conjugates for muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2022-07-12 US disclosed
US-11338041-B2 Exon skipping oligomer conjugates for muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2022-05-24 US disclosed
US-20210338830-A1 EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2021-11-04 US disclosed
US-20210220386-A1 EXON SKIPPING OLIGOMERS AND OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. (US) 2021-07-22 US disclosed
US-20190292208-A1 PROCESSES FOR PREPARING PHOSPHORODIAMIDATE MORPHOLINO OLIGOMERS SAREPTA THERAPEUTICS, INC. (US) 2019-09-26 US disclosed
US-20190262375-A1 EXON SKIPPING OLIGOMERS FOR MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. 2019-08-29 US disclosed
US-10364431-B2 Compositions for treating muscular dystrophy SAREPTA THERAPEUTICS, INC. (US) 2019-07-30 US disclosed
US-20190054113-A1 METHODS FOR TREATING MUSCULAR DYSTROPHY SAREPTA THERAPEUTICS, INC. 2019-02-21 US disclosed
US-20180177814-A1 EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT 2018-06-28 US disclosed
US-20180105811-A1 COMPOSITIONS FOR TREATING MUSCULAR DYSTROPHY JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT 2018-04-19 US disclosed
US-9682097-B2 Oligonucleotide analogues targeting human LMNA SAREPTA THERAPEUTICS, INC. (US) 2017-06-20 US disclosed
US-20170051278-A1 METHODS FOR TREATING PROGEROID LAMINOPATHIES USING OLIGONUCLEOTIDE ANALOGUES TARGETING HUMAN LMNA SAREPTA THERAPEUTICS, INC. 2017-02-23 US disclosed
EP-2799548-A1 ANTISENSE NUCLEIC ACID Nippon Shinyaku Co., Ltd. (JP) 2014-11-05 EP disclosed
US-7264925-B2 Method for analysis of oligonucleotide analogs AVI BIOPHARMA, INC. (US) 2007-09-04 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 (17 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-11338041-B2 Exon skipping oligomer conjugates for muscular dystrophy SMN1; SMN2, UTRN, RBM17 KMT2A 3436/4885MEN1 4296/4885CA2 4821/4885
US-20190054113-A1 METHODS FOR TREATING MUSCULAR DYSTROPHY UTRN, MTPN, MBNL1 KMT2A 1118/4885MEN1 4588/4885CA2 4638/4885
US-20230045831-A1 PROCESSES FOR PREPARING PHOSPHORODIAMIDATE MORPHOLINO OLIGOMERS PPIP5K2, MTAP, RNGTT KMT2A 3884/4885MEN1 1249/4885CA2 4300/4885
US-20230038956-A1 METHODS FOR TREATING MUSCULAR DYSTROPHY UTRN, MTPN, SMN1; SMN2 KMT2A 2239/4885MEN1 4353/4885CA2 4541/4885
US-11382981-B2 Exon skipping oligomer conjugates for muscular dystrophy UTRN, SMN1; SMN2, RBM17 KMT2A 3664/4885MEN1 4270/4885CA2 4841/4885
US-11642364-B2 Exon skipping oligomer conjugates for muscular dystrophy UTRN, SMN1; SMN2, DCLRE1B KMT2A 3663/4885MEN1 4304/4885CA2 4842/4885
US-20210338830-A1 EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY UTRN, SMN1; SMN2, RBM17 KMT2A 3579/4885MEN1 4336/4885CA2 4827/4885
US-20190292208-A1 PROCESSES FOR PREPARING PHOSPHORODIAMIDATE MORPHOLINO OLIGOMERS PPIP5K2, MTAP, RNGTT KMT2A 3884/4885MEN1 1249/4885CA2 4300/4885
US-20210220386-A1 EXON SKIPPING OLIGOMERS AND OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY UTRN, RBM17, SMN1; SMN2 KMT2A 3879/4885MEN1 4584/4885CA2 4823/4885
US-11491238-B2 Exon skipping oligomer conjugates for muscular dystrophy UTRN, SMN1; SMN2, RBM17 KMT2A 3489/4885MEN1 4353/4885CA2 4817/4885
US-20180105811-A1 COMPOSITIONS FOR TREATING MUSCULAR DYSTROPHY MYOF, MTPN, UTRN KMT2A 3679/4885MEN1 4761/4885CA2 4099/4885
US-20220403385-A1 COMPOSITIONS FOR TREATING MUSCULAR DYSTROPHY MYOF, MTPN, UTRN KMT2A 3679/4885MEN1 4761/4885CA2 4099/4885
US-20180177814-A1 EXON SKIPPING OLIGOMER CONJUGATES FOR MUSCULAR DYSTROPHY UTRN, SMN1; SMN2, DCLRE1B KMT2A 3663/4885MEN1 4304/4885CA2 4842/4885
US-20230193282-A1 TREATMENT METHODS FOR MUSCULAR DYSTROPHY MTPN, UTRN, CAPNS1 KMT2A 2776/4885MEN1 3342/4885CA2 905/4885
US-20170051278-A1 METHODS FOR TREATING PROGEROID LAMINOPATHIES USING OLIGONUCLEOTIDE ANALOGUES TARGETING HUMAN LMNA LMNA, LMNB2, LMNB1 KMT2A 2685/4885MEN1 1171/4885CA2 4843/4885
US-10364431-B2 Compositions for treating muscular dystrophy MYOF, MTPN, UTRN KMT2A 3679/4885MEN1 4761/4885CA2 4099/4885
US-20190262375-A1 EXON SKIPPING OLIGOMERS FOR MUSCULAR DYSTROPHY RBM17, UTRN, UPF1 KMT2A 4214/4885MEN1 4539/4885CA2 4778/4885

“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.