Cystetine Triphosphate

Cystetine Triphosphate

SCHEMBL315351

Nc1ccn([C@@H]2O[C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)[C@H](O)[C@H]2O)c(=O)n1

nearest known ligand 0.80

Full drug profile on Sugi Atlas →

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
P2RY2 P41231 13/20 0.80
P2RY6 Q15077 10/20 0.71
P2RY4 P51582 7/20 0.71

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
SCHEMBL376516 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL18784962 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL104629 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
SCHEMBL376515 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL10044131 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL104630 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL105273 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL15810768 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL21311175 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4
Cystetine Triphosphate SCHEMBL4289439 1.00 P2RY2 (0.80) P2RY2P2RY6P2RY4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3752610-B1 POLYRIBONUCLEOTIDE CONTAINING DEUTERATED NUCLEOTIDES ETHRIS GMBH (DE) 2026-01-28 EP claimed
WO-2025060527-A1 3'-SIALYLLACTOSE-PRODUCING ENGINEERED BACTERIUM, AND CONSTRUCTION METHOD AND APPLICATION THEREOF SYNAURA BIOTECHNOLOGY (SHANGHAI) CO., LTD. (CN) 2025-03-27 WO claimed
US-20240368655-A1 CLICK HANDLE-MODIFIED DEOXY-FLUOROARABINO NUCLEIC ACID AS A SYNTHETIC GENETIC POLYMER CAPABLE OF POST-POLYMERIZATION FUNCTIONALIZATION NATIONAL INSTITUTES OF HEALTH 2024-11-07 US claimed
US-20240226335-A9 RNA Containing Modified Nucleosides and Methods of Use Thereof THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA 2024-07-11 US claimed
US-20240131194-A1 RNA Containing Modified Nucleosides and Methods of Use Thereof UNIV PENNSYLVANIA (US) 2024-04-25 US claimed
CN-115060823-B Method for separating nucleoside triphosphates and/or deoxynucleoside triphosphates by HPLC 生工生物工程(上海)股份有限公司 2023-06-02 CN claimed
CN-115060823-A Method for separating nucleoside triphosphates and/or deoxynucleoside triphosphates by HPLC 生工生物工程(上海)股份有限公司 2022-09-16 CN claimed
US-11389547-B2 RNA containing modified nucleosides and methods of use thereof THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2022-07-19 US claimed
US-11246965-B2 Compositions and methods for reducing neointima formation UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2022-02-15 US claimed
CN-111635532-B Aggregation-induced fluorescence guest functionalized composite infinite coordination polymer nanoparticle and preparation and application thereof 华东师范大学 2021-07-27 CN claimed
EP-1624059-A2 Method of producing nucleic acid molecules with reduced secondary structure Agilent Technologies, Inc. (US) 2006-02-08 EP claimed
US-20040086880-A1 Method of producing nucleic acid molecules with reduced secondary structure AGILENT TECHNOLOGIES, INC. 2004-05-06 US claimed
EP-1025115-B1 NOVEL NUCLEOSIDE OR NUCLEOTIDE FLUORESCENT CONJUGATES, PREPARATION METHOD AND USES CIS BIO INT (FR) 2003-06-04 EP claimed
US-20030027785-A1 Joint lubrication with P2Y purinergic receptor agonists INSPIRE PHARMACEUTICALS, INC. 2003-02-06 US claimed
EP-0897301-B1 METHOD OF TREATING OTITIS MEDIA WITH URIDINE TRIPHOSPHATES AND RELATED COMPOUNDS INSPIRE PHARMACEUTICALS INC (US) 2002-10-09 EP claimed
WO-2001077366-A1 POSITIVE SELECTION METHOD, COMPOUNDS, HOST CELLS AND USES THEREOF CUBIST PHARMACEUTICALS, INC. (US) 2001-10-18 WO claimed
EP-1025115-A1 NOVEL NUCLEOSIDE OR NUCLEOTIDE FLUORESCENT CONJUGATES, PREPARATION METHOD AND USES CIS BIO INTERNATIONAL (FR) 2000-08-09 EP claimed
WO-1999018114-A1 NOVEL NUCLEOSIDE OR NUCLEOTIDE FLUORESCENT CONJUGATES, PREPARATION METHOD AND USES CIS BIO INTERNATIONAL (FR) 1999-04-15 WO claimed
EP-0524143-B1 Process of preparation of activated sialic acids CIBA GEIGY AG (CH) 1997-12-10 EP claimed
US-RE28886-E Method for preparing cytidine diphosphate choline KYOWA HAKKO KOGYO CO., LTD. (JA) 1976-06-29 US claimed

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-11246965-B2 Compositions and methods for reducing neointima formation CTPS1, CTPS2, TNNI3 P2RY2 1867/4885P2RY6 1518/4885P2RY4 1902/4885
US-20240368655-A1 CLICK HANDLE-MODIFIED DEOXY-FLUOROARABINO NUCLEIC ACID AS A SYNTHETIC GENETIC POLYMER CAPABLE OF POST-POLYMERIZATION FUNCTIONALIZATION RNGTT, UNG, DCTD P2RY2 1794/4885P2RY6 1163/4885P2RY4 991/4885
US-20030027785-A1 Joint lubrication with P2Y purinergic receptor agonists P2RY1, P2RY2, P2RY6 P2RY2 2/4885P2RY6 3/4885P2RY4 5/4885

“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.