Ribose (Furanose)

Ribose (Furanose)

SCHEMBL346135

Nc1nc[nH]c(=O)n1.OC[C@H]1OC(O)[C@@H](O)[C@@H]1O

nearest known ligand 0.49

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.49
MTOR P42345 2/20 0.49
ALDH1A1 P00352 2/20 0.49
DNMT1 P26358 2/20 0.49
TP53 P04637 2/20 0.49
GMNN O75496 1/20 0.49
NFKB1 P19838 1/20 0.49
THPO P40225 1/20 0.49
HTT P42858 1/20 0.49
RAB9A P51151 1/20 0.49
BLM P54132 1/20 0.49
HBB P68871 1/20 0.49
PMP22 Q01453 1/20 0.49
THRB P10828 1/20 0.43
MDM2 Q00987 1/20 0.43
NCOA1 Q15788 1/20 0.43
NCOA3 Q9Y6Q9 1/20 0.43
PNP P00491 4/20 0.43
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41

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
Ribose (Furanose) SCHEMBL10787751 1.00 LMNA (0.49) LMNAMTORALDH1A1DNMT1TP53
Ribose (Furanose) SCHEMBL8833 0.78 LMNA (0.49) LMNAMTORALDH1A1DNMT1TP53
Ribose (Furanose) SCHEMBL3341287 0.78 LMNA (0.49) LMNAMTORALDH1A1DNMT1TP53
Ribose (Furanose) SCHEMBL2325834 0.78 LMNA (0.49) LMNAMTORALDH1A1DNMT1TP53
Ribose (Furanose) SCHEMBL142622 0.78 LMNA (0.49) LMNAMTORALDH1A1DNMT1TP53
2-Aminopurine SCHEMBL5529464 0.77 LMNA (0.41) LMNAMTORALDH1A1DNMT1TP53
2-Aminopurine SCHEMBL28775710 0.77 ALDH1A1 (0.59) LMNAMTORALDH1A1DNMT1TP53
Ribose (Furanose) SCHEMBL16620262 0.77 PNP (0.44) LMNAMTORALDH1A1DNMT1TP53
Isoguanine SCHEMBL11527542 0.77 PNP (0.39) LMNAMTORALDH1A1DNMT1TP53
Ribose (Furanose) SCHEMBL628713 0.77 LMNA (0.48) LMNAMTORALDH1A1DNMT1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170231911-A1 METHODS AND COMPOSITIONS FOR IMPROVING OUTCOMES OF LIPOSOMAL CHEMOTHERAPY MERRIMACK PHARMACEUTICALS, INC. 2017-08-17 US claimed
WO-2014169067-A1 COMPOSITIONS FOR IMPROVING OUTCOMES OF LIPOSOMAL CHEMOTHERAPY MERRIMACK PHARMACEUTICALS, INC. (US) 2014-10-16 WO claimed
US-8580857-B2 Methods and compositions to determine the chemosensitizing dose of suramin used in combination therapy AU JESSIE L-S (US) 2013-11-12 US claimed
US-20110142794-A1 Methods and Compositions to Determine the Chemosensitizing Dose of Suramin Used in Combination Therapy AU JESSIE L-S 2011-06-16 US claimed
US-7309696-B2 Compositions and methods for targeting cancer cells WAKE FOREST UNIVERSITY (US) 2007-12-18 US claimed
EP-1429713-A4 METHODS AND COMPOSITIONS TO DETERMINE THE CHEMOSENSITIZING DOSE OF SURAMIN USED IN COMBINATION THERAPY AU JESSIE L S (US) 2007-08-08 EP claimed
WO-2007011760-A2 INHIBITORS OF MITOTIC KINESIN KALYPSYS, INC. (US) 2007-01-25 WO claimed
WO-2007011759-A2 INHIBITORS OF MITOTIC KINESIN KALYPSYS, INC. (US) 2007-01-25 WO claimed
WO-2007011721-A1 INHIBITORS OF MITOTIC KINESIN KALYPSYS, INC. (US) 2007-01-25 WO claimed
US-20040180955-A1 Methods and compositions to determine the chemosensitizing dose of suramin used in combination therapy AU JESSIE L-S (US) 2004-09-16 US claimed
EP-1429713-A2 METHODS AND COMPOSITIONS TO DETERMINE THE CHEMOSENSITIZING DOSE OF SURAMIN USED IN COMBINATION THERAPY Au, Jessie L.S. (US) 2004-06-23 EP claimed
EP-0909184-B1 TARGETED DRUG DELIVERY USING SULFONAMIDE DERIVATIVES UPJOHN CO (US) 2003-09-17 EP claimed
WO-2003026574-A2 METHODS AND COMPOSITIONS TO DETERMINE THE CHEMOSENSITIZING DOSE OF SURAMIN USED IN COMBINATION THERAPY AU JESSIE L-S (US) 2003-04-03 WO claimed
US-4684630-A WATER UNSTABLE AZACYTIDINE AND 5-AZACYTOSINE ARABINOSE IN AN AQUEOUS DILUTED DMSO AND DIMETHYLACETAMIDE SOLUTION REPTA ARNOLD J 1987-08-04 US claimed
CN-117441022-A Sequential electroporation method 美克斯细胞有限公司 2024-01-23 CN disclosed
US-20230390422-A1 OLIGONUCLEOTIDE-BASED THERAPEUTICS AND USES THEREOF SPEER TOD (US) 2023-12-07 US disclosed
EP-4218730-B1 LIPOSOMES USEFUL FOR DRUG DELIVERY IPSEN BIOPHARM LTD (GB) 2023-11-01 EP disclosed
US-5216011-A Solvent mixture consisting of propylene glycol and water BRISTOL-MYERS SQUIBB CO. (US) 1993-06-01 US disclosed
EP-0415430-A1 Stable solutions of mitomycin C Bristol-Myers Squibb Company (US) 1991-03-06 EP disclosed
US-4684630-A WATER UNSTABLE AZACYTIDINE AND 5-AZACYTOSINE ARABINOSE IN AN AQUEOUS DILUTED DMSO AND DIMETHYLACETAMIDE SOLUTION REPTA ARNOLD J 1987-08-04 US 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 (2 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-20230390422-A1 OLIGONUCLEOTIDE-BASED THERAPEUTICS AND USES THEREOF POLRMT, DCLRE1B, POLM LMNA 337/4885MTOR 4672/4885ALDH1A1 3320/4885
US-20170231911-A1 METHODS AND COMPOSITIONS FOR IMPROVING OUTCOMES OF LIPOSOMAL CHEMOTHERAPY LIPA, SGMS1, SGMS2 LMNA 2531/4885MTOR 3742/4885ALDH1A1 3841/4885

“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.