SCHEMBL16094299

SCHEMBL16094299

NCCCCCCCCCCCCCCOOOOOOC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ DOT1L Q8TEK3 3/20 0.62
▸ DNMT3B Q9UBC3 2/20 0.62
▸ PRMT7 Q9NVM4 1/20 0.62
▸ P2RY1 P47900 4/20 0.60
▸ SRM P19623 3/20 0.60
▸ ADORA1 P30542 3/20 0.60
▸ SMN1; SMN2 Q16637 3/20 0.60
▸ P2RY2 P41231 3/20 0.60
▸ ADORA3 P0DMS8 2/20 0.60
▸ ADORA2A P29274 2/20 0.60
▸ ADORA2B P29275 2/20 0.60
▸ SRC P12931 2/20 0.60
▸ DPP4 P27487 1/20 0.60
▸ MEN1 O00255 1/20 0.60
▸ SLC28A1 O00337 1/20 0.60
▸ MAP3K7 O43318 1/20 0.60
▸ SLC28A2 O43868 1/20 0.60
▸ GAPDH P04406 1/20 0.60
▸ MAPK1 P28482 1/20 0.60
▸ STAT6 P42226 1/20 0.60

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
SCHEMBL8007640 0.93 DOT1L (0.65) DOT1LDNMT3BPRMT7P2RY1SRM
SCHEMBL10886673 0.89 DOT1L (0.66) DOT1LDNMT3BPRMT7P2RY1SRM
SCHEMBL31001584 0.84 P2RY1 (0.61) DOT1LDNMT3BPRMT7P2RY1SRM
SCHEMBL4819105 0.83 P2RY1 (0.70) P2RY1ADORA1SMN1; SMN2P2RY2SRC
SCHEMBL1513014 0.83 P2RY1 (0.77) P2RY1ADORA1SMN1; SMN2P2RY2SRC
SCHEMBL6247323 0.82 AHCY (0.71) DOT1LP2RY1ADORA1SMN1; SMN2P2RY2
SCHEMBL6828798 0.82 ADORA1 (0.70) DOT1LDNMT3BPRMT7P2RY1ADORA1
SCHEMBL8388991 0.82 DOT1L (0.66) DOT1LDNMT3BPRMT7P2RY1SRM
SCHEMBL481524 0.82 ADORA1 (0.76) DOT1LP2RY1ADORA1SMN1; SMN2P2RY2
SCHEMBL2040670 0.82 ADORA1 (0.76) DOT1LP2RY1ADORA1SMN1; SMN2P2RY2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024151975-A1 DETECTING DEGRADATION OF A POLYNUCLEOTIDE BY RAMAN SPECTROSCOPY LEDNEV IGOR (US) 2024-07-18 — — WO disclosed
US-11980672-B2 Heterologous UTR sequences for enhanced mRNA expression MODERNATX, INC. (US) 2024-05-14 — — US disclosed
EP-4351623-A1 GENE COMBINATION AS A BROAD SPECTRUM ANTIVIRAL Icahn School of Medicine at Mount Sinai (US) 2024-04-17 — — EP disclosed
US-20240100188-A1 REGULATORY SYSTEM FOR EXPRESSION OF A GENE OF INTEREST IN A TARGET CELL AND METHOD OF USE THEREOF ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2024-03-28 — — US disclosed
WO-2024015729-A1 REGULATORY SYSTEM FOR EXPRESSION OF A GENE OF INTEREST IN A TARGET CELL AND METHOD OF USE THEREOF ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2024-01-18 — — WO disclosed
WO-2023235568-A1 DERIVATION OF GLUCOSE-RESPONSIVE INSULIN-SECRETING CELLS AND ORGANOIDS FROM HUMAN STOMACH CELLS AND THEIR USE TO TREAT DIABETES CORNELL UNIVERSITY (US) 2023-12-07 — — WO disclosed
WO-2023192932-A2 INDUCED LIVER SINUSOIDAL ENDOTHELIAL CELLS (iLSECs) AND METHODS FOR SUPPORTING HEPATOCYTES USING THE iLSECs CORNELL UNIVERSITY (US) 2023-10-05 — — WO disclosed
US-20230050143-A1 Heterologous UTR Sequences for Enhanced mRNA Expression MODERNATX, INC. (US) 2023-02-16 — — US disclosed
US-20230008266-A1 SYNTHETIC MODIFIED RNA AND USES THEREOF ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2023-01-12 — — US disclosed
WO-2022261206-A1 GENE COMBINATION AS A BROAD SPECTRUM ANTIVIRAL ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2022-12-15 — — WO disclosed
EP-3423106-A1 BIODEGRADABLE ACTIVATED POLYMERS FOR THERAPEUTIC DELIVERY Alexion Pharmaceuticals, Inc. (US) 2019-01-09 — — EP disclosed
US-20180353618-A1 Heterologous UTR Sequences for Enhanced mRNA Expression MODERNATX, INC. (US) 2018-12-13 — — US disclosed
US-10138507-B2 Manufacturing methods for production of RNA transcripts MODERNATX, INC. (US) 2018-11-27 — — US disclosed
EP-3386533-A1 MODIFIED MRNA ENCODING A URIDINE DIPHOPSPHATE GLUCURONOSYL TRANSFERASE AND USES THEREOF ModernaTX, Inc. (US) 2018-10-17 — — EP disclosed
WO-2017100562-A9 MODIFIED MRNA ENCODING A URIDINE DIPHOPSPHATE GLUCURONOSYL TRANSFERASE AND USES THEREOF ALEXION PHARMACEUTICALS, INC, (US) 2017-08-03 — — WO disclosed
WO-2017100562-A1 MODIFIED MRNA ENCODING A URIDINE DIPHOPSPHATE GLUCURONOSYL TRANSFERASE AND USES THEREOF ALEXION PHARMACEUTICALS, INC, (US) 2017-06-15 — — WO disclosed
WO-2017100551-A1 HETEROLOGOUS UTR SEQUENCES FOR ENHANCED mRNA EXPRESSION ALEXION PHARMACEUTICALS, INC. (US) 2017-06-15 — — WO disclosed
US-20160024547-A1 MANUFACTURING METHODS FOR PRODUCTION OF RNA TRANSCRIPTS ARES CAPITAL CORPORATION, AS AGENT 2016-01-28 — — US disclosed
EP-2971033-A1 MANUFACTURING METHODS FOR PRODUCTION OF RNA TRANSCRIPTS Moderna Therapeutics, Inc. (US) 2016-01-20 — — EP disclosed
WO-2014152027-A1 MANUFACTURING METHODS FOR PRODUCTION OF RNA TRANSCRIPTS MODERNA THERAPEUTICS, INC. (US) 2014-09-25 — — WO 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-20230050143-A1 Heterologous UTR Sequences for Enhanced mRNA Expression RNGTT, UPF1, RNMT DOT1L 4741/4885DNMT3B 1310/4885PRMT7 2667/4885
US-20180353618-A1 Heterologous UTR Sequences for Enhanced mRNA Expression RNGTT, UPF1, RNMT DOT1L 4741/4885DNMT3B 1310/4885PRMT7 2667/4885
US-11980672-B2 Heterologous UTR sequences for enhanced mRNA expression RNGTT, UPF1, RNMT DOT1L 4741/4885DNMT3B 1310/4885PRMT7 2667/4885

“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.

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