Kinetin Riboside

Kinetin Riboside

SCHEMBL3190252

OC[C@H]1O[C@@H](n2cnc3c(NCc4ccco4)ncnc32)[C@H](O)[C@@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ ADORA3 P0DMS8 6/20 1.00
▸ SLC29A1 Q99808 4/20 1.00
▸ TP53 P04637 3/20 1.00
▸ PAX8 Q06710 3/20 1.00
▸ SMN1; SMN2 Q16637 1/20 1.00
▸ MITF O75030 1/20 1.00
▸ LMNA P02545 1/20 1.00
▸ TDP1 Q9NUW8 1/20 0.74
▸ ADORA2A P29274 3/20 0.69
▸ ADORA1 P30542 3/20 0.69
▸ TSHR P16473 1/20 0.69
▸ NFKB1 P19838 1/20 0.69
▸ STAT6 P42226 1/20 0.69
▸ GMNN O75496 1/20 0.69
▸ BLM P54132 1/20 0.69
▸ PMP22 Q01453 1/20 0.69
▸ ADORA2B P29275 1/20 0.67

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
Kinetin Riboside SCHEMBL217034 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL17825970 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL29564117 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL3339041 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL14713232 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL3190271 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL19583061 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
Kinetin Riboside SCHEMBL14713468 1.00 ADORA3 (1.00) ADORA3SLC29A1TP53PAX8SMN1; SMN2
SCHEMBL25170466 0.99 ADORA3 (0.98) ADORA3SLC29A1TP53PAX8SMN1; SMN2
SCHEMBL29697393 0.99 ADORA3 (0.98) ADORA3SLC29A1TP53PAX8SMN1; 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 42 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104382924-A N6-substituted adenosine derivative and N6-substituted adenine derivative and application thereof INST MATERIA MEDICA CAMS 2015-03-04 — — CN claimed
US-12378247-B2 Mesylate salt of para-topolin, compositions containing said salt and use thereof USTAV EXPERIMENTALNI BOTANIKY AV CR, V. V. I. (CZ) 2025-08-05 — — US disclosed
EP-3229771-B1 6-ARYL-9-GLYCOSYLPURINES AND USE THEREOF UNIV PALACKEHO (CZ) 2024-04-03 — — EP disclosed
US-11702417-B2 Compounds for improving mRNA splicing THE GENERAL HOSPITAL CORPORATION (US) 2023-07-18 — — US disclosed
US-11702417-B2 Compounds for improving mRNA splicing THE GENERAL HOSPITAL CORPORATION (US) 2023-07-18 — — US disclosed
US-20230055908-A1 MESYLATE SALT OF PARA-TOPOLIN, COMPOSITIONS CONTAINING SAID SALT AND USE THEREOF USTAV EXPERIMENTALNI BOTANIKY AV CR, V. V. I. (CZ) 2023-02-23 — — US disclosed
EP-4115882-A1 COMPOUNDS FOR IMPROVING MRNA SPLICING The General Hospital Corporation (US) 2023-01-11 — — EP disclosed
US-20220339179-A1 TREATMENT OF HR DEFICIENT CANCER THE FRANCIS CRICK INSTITUTE LIMITED (GB) 2022-10-27 — — US disclosed
EP-4028009-A1 TREATMENT OF HR DEFICIENT CANCER The Francis Crick Institute Limited (GB) 2022-07-20 — — EP disclosed
EP-3341371-B1 ADENINE DERIVATIVES AND THEIR USE AS UV-PHOTOPROTECTIVE AGENTS UNIV PALACKEHO (CZ) 2022-06-29 — — EP disclosed
US-20080267948-A1 Croos-B Structure Binding Compounds CROSSBETA BIOSCIENCES B.V. (NL) 2008-10-30 — — US disclosed
WO-2008045955-A9 INHIBITING CYCLIN D POLYPEPTIDES MAYO FOUNDATION (US) 2008-10-02 — — WO disclosed
WO-2008045955-A2 INHIBITING CYCLIN D POLYPEPTIDES MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2008-04-17 — — WO disclosed
US-20070042030-A1 Preparation for the application of agents in mini-droplets IDEA AG (DE) 2007-02-22 — — US disclosed
EP-0475160-B2 Preparation for drug application in minute droplet form IDEA AG (DE) 2004-07-14 — — EP disclosed
US-6165500-A Preparation for the application of agents in mini-droplets IDEA AG (DE) 2000-12-26 — — US disclosed
EP-0475160-B1 Preparation for drug application in minute droplet form IDEA AG (DE) 1996-02-14 — — EP disclosed
EP-0475160-A1 Preparation for drug application in minute droplet form Cevc, Gregor, Prof. Dr. (DE) 1992-03-18 — — EP disclosed
WO-1992003122-A1 PREPARATION FOR APPLICATION OF ACTIVE SUBSTANCES IN THE FORM OF MINIMUM-SIZED DROPLETS CEVC GREGOR (DE) 1992-03-05 — — WO disclosed
EP-0355825-A2 Viral treatment system Prendergast, Patrick T. (IE) 1990-02-28 — — 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-20230055908-A1 MESYLATE SALT OF PARA-TOPOLIN, COMPOSITIONS CONTAINING SAID SALT AND USE THEREOF TOP2A, TOP1, TOP2B ADORA3 4571/4885SLC29A1 963/4885TP53 6/4885
US-20080267948-A1 Croos-B Structure Binding Compounds CACYBP, TBCB, MYCBP ADORA3 1337/4885SLC29A1 1658/4885TP53 2046/4885
US-11702417-B2 Compounds for improving mRNA splicing RTCB, RBM17, HNRNPA2B1 ADORA3 2060/4885SLC29A1 2394/4885TP53 3333/4885
US-12378247-B2 Mesylate salt of para-topolin, compositions containing said salt and use thereof TOP2A, TOP1, TOP2B ADORA3 4571/4885SLC29A1 963/4885TP53 6/4885
US-20070042030-A1 Preparation for the application of agents in mini-droplets FABP4, NPC1L1, LIPA ADORA3 1717/4885SLC29A1 631/4885TP53 3863/4885

“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.

Send feedback