SCHEMBL2177463

SCHEMBL2177463

C#CN1C(=O)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=CC1N

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 6/20 0.39
▸ SMN1; SMN2 Q16637 4/20 0.39
▸ ALDH1A1 P00352 3/20 0.39
▸ MTOR P42345 2/20 0.39
▸ THPO P40225 2/20 0.39
▸ PMP22 Q01453 2/20 0.39
▸ THRB P10828 1/20 0.39
▸ MDM2 Q00987 1/20 0.39
▸ NCOA1 Q15788 1/20 0.39
▸ NCOA3 Q9Y6Q9 1/20 0.39
▸ POLB P06746 1/20 0.39
▸ GMNN O75496 1/20 0.39
▸ TP53 P04637 1/20 0.39
▸ NFKB1 P19838 1/20 0.39
▸ DNMT1 P26358 1/20 0.39
▸ HTT P42858 1/20 0.39
▸ RAB9A P51151 1/20 0.39
▸ BLM P54132 1/20 0.39
▸ HBB P68871 1/20 0.39
▸ CDA P32320 4/20 0.39

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
SCHEMBL40870 0.81 LMNA (0.41) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL6424353 0.73 CDA (0.45) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL288668 0.72 LMNA (0.42) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL20459913 0.71 LMNA (0.33) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL20833069 0.70 CDA (0.47) LMNAMTORTHRBMDM2NCOA1
SCHEMBL6674416 0.70 CDA (0.47) LMNAMTORTHRBMDM2NCOA1
SCHEMBL17722383 0.69 SLC28A1 (0.42) SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL18503533 0.68 LMNA (0.41) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL17440122 0.68 CDA (0.41) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL18503534 0.68 LMNA (0.43) LMNASMN1; SMN2ALDH1A1MTORTHPO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1594987-A2 NUCLEIC ACID SEQUENCING METHODS, KITS AND REAGENTS Hoser, Mark J. (GB) 2005-11-16 — — EP claimed
WO-2004074503-A2 NUCLEIC ACID SEQUENCING METHODS, KITS AND REAGENTS HOSER MARK J (GB) 2004-09-02 — — WO claimed
US-20230330260-A1 RNA FORMULATIONS ModemaTX, Inc. (US) 2023-10-19 — — US disclosed
US-11446398-B2 Regulated biocircuit systems OBSIDIAN THERAPEUTICS, INC. (US) 2022-09-20 — — US disclosed
EP-3981437-A1 NUCLEIC ACID VACCINES ModernaTX, Inc. (US) 2022-04-13 — — EP disclosed
EP-3638215-A1 RNA FORMULATIONS Modernatx, Inc. (US) 2020-04-22 — — EP disclosed
EP-3625246-A1 POLYNUCLEOTIDES ENCODING TETHERED INTERLEUKIN-12 (IL12) POLYPEPTIDES AND USES THEREOF ModernaTX, Inc. (US) 2020-03-25 — — EP disclosed
US-20190192691-A1 REGULATED BIOCIRCUIT SYSTEMS OBSIDIAN THERAPEUTICS, INC. 2019-06-27 — — US disclosed
EP-3458590-A1 POLYNUCLEOTIDES ENCODING -GALACTOSIDASE A FOR THE TREATMENT OF FABRY DISEASE Modernatx, Inc. (US) 2019-03-27 — — EP disclosed
EP-3458105-A1 POLYNUCLEOTIDES ENCODING GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE FOR THE TREATMENT OF GALACTOSEMIA TYPE 1 Modernatx, Inc. (US) 2019-03-27 — — EP disclosed
EP-3458083-A1 POLYNUCLEOTIDES ENCODING INTERLEUKIN-12 (IL12) AND USES THEREOF Modernatx, Inc. (US) 2019-03-27 — — EP disclosed
WO-2015034928-A1 CHIMERIC POLYNUCLEOTIDES MODERNA THERAPEUTICS, INC. (US) 2015-03-12 — — WO disclosed
EP-2641605-A1 NOVEL POLYMER DERIVATIVE OF CYTIDINE METABOLISM ANTAGONIST Nippon Kayaku Kabushiki Kaisha (JP) 2013-09-25 — — EP disclosed
WO-2011079501-A1 PRODRUG BASED ON CYTARABINE STRUCTURE AS WELL AS SYNTHESIZING METHOD AND APPLICATION THEREOF 济南圣鲁金药物技术开发有限公司 (CN) 2011-07-07 — — WO disclosed
CN-102115485-A Prodrug based on cytosine arabinoside structure, and synthesis method and application thereof SANLUGEN PHARMATECH 2011-07-06 — — CN disclosed
CN-101525361-B Prodrug based on gemcitabine structure as well as synthesizing method and application thereof JINAN SHENGLUJIN PHARMACEUTICAL TECHNOLOGY DEV CO LTD 2010-11-17 — — CN disclosed
CN-101525361-A Prodrug based on gemcitabine structure as well as synthesizing method and application thereof SANLUGEN PHARMATECH DEV CO LTD 2009-09-09 — — CN disclosed
CN-101490076-A 3' -ethynylcytosine nucleoside derivatives TAIHO PHARMACEUTICAL CO LTD (JP) 2009-07-22 — — CN disclosed
EP-1594987-A2 NUCLEIC ACID SEQUENCING METHODS, KITS AND REAGENTS Hoser, Mark J. (GB) 2005-11-16 — — EP disclosed
WO-2004074503-A2 NUCLEIC ACID SEQUENCING METHODS, KITS AND REAGENTS HOSER MARK J (GB) 2004-09-02 — — 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 (1 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-20230330260-A1 RNA FORMULATIONS SYNCRIP, NSUN3, RNMT LMNA 700/4885SMN1; SMN2 273/4885ALDH1A1 4010/4885

“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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