SCHEMBL2056757

SCHEMBL2056757

Cc1cn([C@H]2CC(O[Si](C)(C)C(C)(C)C)[C@@H](CO)O2)c(=O)[nH]c1=O

nearest known ligand 0.64

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
RNASE1 P07998 1/20 0.62
TK1 P04183 5/20 0.59
LMNA P02545 2/20 0.57
TSHR P16473 2/20 0.57
ALB P02768 1/20 0.57
PKM P14618 1/20 0.57
BLM P54132 1/20 0.57
PMP22 Q01453 1/20 0.57
CYP2D6 P10635 1/20 0.57
TK2 O00142 1/20 0.56

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
SCHEMBL15354282 1.00 RNASE1 (0.62) RNASE1TK1LMNATSHRALB
SCHEMBL25747162 1.00 RNASE1 (0.62) RNASE1TK1LMNATSHRALB
SCHEMBL25797545 1.00 RNASE1 (0.62) RNASE1TK1LMNATSHRALB
SCHEMBL24059196 1.00 RNASE1 (0.62) RNASE1TK1LMNATSHRALB
SCHEMBL733403 1.00 RNASE1 (0.62) RNASE1TK1LMNATSHRALB
SCHEMBL24059145 1.00 RNASE1 (0.62) RNASE1TK1LMNATSHRALB
SCHEMBL8424862 0.92 RNASE1 (0.53) RNASE1TK1LMNAALBPKM
SCHEMBL8424863 0.92 RNASE1 (0.53) RNASE1TK1LMNAALBPKM
SCHEMBL10079072 0.91 TOP2A (0.54) RNASE1TK1
SCHEMBL14788961 0.91 TOP2A (0.54) RNASE1TK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12398170-B2 Nucleoside derivative and use thereof NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM (JP) 2025-08-26 US disclosed
US-20250215040-A1 METHOD AND COMPOUND ATDBio Limited (GB) 2025-07-03 US disclosed
US-12202848-B2 Phosphoramidite activator FUJIFILM WAKO PURE CHEMICAL CORPORATION (JP) 2025-01-21 US disclosed
US-20240166674-A1 PHOSPHORAMIDITE ACTIVATOR FUJIFILM WAKO PURE CHEMICAL CORPORATION (JP) 2024-05-23 US disclosed
CN-114555617-B Phosphoramidite activators 富士胶片和光纯药株式会社 2024-03-08 CN disclosed
EP-4047004-B1 PHOSPHORAMIDITE ACTIVATOR FUJIFILM WAKO PURE CHEMICAL CORP (JP) 2024-03-06 EP disclosed
WO-2024010870-A2 CRYSTALLINE MONOMERS FOR PREPARING ANTISENSE OLIGONUCLEOTIDES AND METHODS OF THEIR PREPARATION AND USE EISAI R&D MANAGEMENT CO., LTD. (JP) 2024-01-11 WO disclosed
US-20230374058-A1 COMPOUNDS AND METHODS FOR TREATING DISEASE ROME THERAPEUTICS, INC. 2023-11-23 US disclosed
WO-2023178133-A9 COMPOUNDS AND METHODS FOR TREATING DISEASE ROME THERAPEUTICS, INC. (US) 2023-10-26 WO disclosed
WO-2023180237-A1 METHOD AND COMPOUND ATDBio Limited (GB) 2023-09-28 WO disclosed
US-5218102-A Easily synthesized, hybridize well with target sequences IMPROBIO (BE) 1993-06-08 US disclosed
EP-0541722-A1 COMPOUNDS AND METHODS FOR INHIBITING GENE EXPRESSION. STERLING WINTHROP INC (US) 1993-05-19 EP disclosed
WO-1993006120-A1 PHOSPHORAMIDATE ANALOGS OF 5-FLUORO-2'-DEOXYURIDINE UNIVERSITY OF ROCHESTER (US) 1993-04-01 WO disclosed
US-5192749-A Viricide, AIDS SYNTEX (U.S.A.) INC. (US) 1993-03-09 US disclosed
WO-1992013869-A1 METHYLENE PHOSPHONATE NUCLEOSIDE ANALOGS AND OLIGONUCLEOTIDE ANALOGS MADE THEREFROM GILEAD SCIENCES, INC. (US) 1992-08-20 WO disclosed
WO-1992002534-A2 COMPOUNDS AND METHODS FOR INHIBITING GENE EXPRESSION STERLING DRUG, INC. (US) 1992-02-20 WO disclosed
US-5026838-A Starting materials for polynucleotides NIPPON ZEON CO., LTD. (JP) 1991-06-25 US disclosed
US-4914193-A INTERMEDIATES FOR OLIGODEOXYNUCLEOTIDES TOAGOSEI CHEMICAL INDUSTRY CO., LTD. (JP) 1990-04-03 US disclosed
EP-0334694-A1 Nucleic acid probes with non-radioactive labels, and preparation processes LA REGION WALLONNE (BE) 1989-09-27 EP disclosed
EP-0216357-A2 Phosphoramidite compounds and process for production thereof NIPPON ZEON CO., LTD. (JP) 1987-04-01 EP 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 (5 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-20230374058-A1 COMPOUNDS AND METHODS FOR TREATING DISEASE EHMT1, POLRMT, RNASE1 RNASE1 3/4885TK1 37/4885LMNA 2032/4885
US-20240166674-A1 PHOSPHORAMIDITE ACTIVATOR ITPA, INPP5D, INPP5B RNASE1 1474/4885TK1 101/4885LMNA 4192/4885
US-12398170-B2 Nucleoside derivative and use thereof NT5C3B, NUDT1, PNP RNASE1 269/4885TK1 327/4885LMNA 3363/4885
US-12202848-B2 Phosphoramidite activator ITPA, INPP5D, INPP5B RNASE1 1474/4885TK1 101/4885LMNA 4192/4885
US-20250215040-A1 METHOD AND COMPOUND POLN, POLRMT, FBL RNASE1 38/4885TK1 322/4885LMNA 186/4885

“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.