SCHEMBL288668

SCHEMBL288668

NC1C=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(=O)S1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 6/20 0.42
▸ SMN1; SMN2 Q16637 4/20 0.42
▸ ALDH1A1 P00352 3/20 0.42
▸ MTOR P42345 2/20 0.42
▸ THPO P40225 2/20 0.42
▸ PMP22 Q01453 2/20 0.42
▸ THRB P10828 1/20 0.42
▸ MDM2 Q00987 1/20 0.42
▸ NCOA1 Q15788 1/20 0.42
▸ NCOA3 Q9Y6Q9 1/20 0.42
▸ POLB P06746 1/20 0.42
▸ GMNN O75496 1/20 0.42
▸ TP53 P04637 1/20 0.42
▸ NFKB1 P19838 1/20 0.42
▸ DNMT1 P26358 1/20 0.42
▸ HTT P42858 1/20 0.42
▸ RAB9A P51151 1/20 0.42
▸ BLM P54132 1/20 0.42
▸ HBB P68871 1/20 0.42
▸ CDA P32320 4/20 0.42

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
SCHEMBL6424353 0.77 CDA (0.45) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL6364684 0.76 LMNA (0.44) LMNASMN1; SMN2PMP22DNMT1BLM
SCHEMBL40870 0.75 LMNA (0.41) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL20833069 0.73 CDA (0.47) LMNAMTORTHRBMDM2NCOA1
SCHEMBL6674416 0.73 CDA (0.47) LMNAMTORTHRBMDM2NCOA1
SCHEMBL18503533 0.72 LMNA (0.41) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL2177463 0.72 LMNA (0.39) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL18503534 0.71 LMNA (0.43) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL8600538 0.69 CDA (0.47) LMNASMN1; SMN2ALDH1A1MTORTHPO
SCHEMBL8600543 0.69 CDA (0.47) 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 66 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1993017035-A1 2'ISODIDEOXY-β-D-NUCLEOSIDES AS STABLE ANTIVIRAL AGENTS UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 1993-09-02 — — WO claimed
US-20210002202-A1 Substituted Aromatic Compounds and Pharmaceutical Uses Thereof PROMETIC BIOSCIENCES, INC. (CA) 2021-01-07 — — US disclosed
US-10815183-B2 Substituted aromatic compounds and pharmaceutical uses thereof PROMETIC PHARMA SMT LIMITED (GB) 2020-10-27 — — US disclosed
US-20180162799-A1 SUBSTITUTED AROMATIC COMPOUNDS AND PHARMACEUTICAL USES THEREOF PROMETIC PHARMA SMT LIMITED (GB) 2018-06-14 — — US disclosed
US-9938221-B2 Substituted aromatic compounds and pharmaceutical uses thereof PROMETIC PHARMA SMT LIMITED (GB) 2018-04-10 — — US disclosed
EP-2299998-B1 MEDIUM-CHAIN LENGTH FATTY ACIDS AND GLYCERIDES AS NEPHROPROTECTION AGENTS PROMETIC PHARMA SMT LTD (GB) 2018-01-03 — — EP disclosed
EP-2632885-B1 PHENYLKETONE CARBOXYLATE COMPOUNDS AND PHARMACEUTICAL USES THEREOF PROMETIC PHARMA SMT LTD (GB) 2018-01-03 — — EP disclosed
US-9738678-B2 Substituted nucleoside derivatives with antiviral and antimicrobial properties EASTERN VIRGINIA MEDICAL SCHOOL (US) 2017-08-22 — — US disclosed
US-9682054-B2 Medium-chain length fatty acids, glycerides and analogues as stimulators of erythropoiesis PROMETIC PHARMA SMT LIMITED (GB) 2017-06-20 — — US disclosed
US-9532962-B2 Medium-chain length fatty acids and glycerides as nephroprotection agents PROMETIC PHARMA SMT LIMITED (GB) 2017-01-03 — — US disclosed
WO-2002083120-A2 MEDIUM-CHAIN LENGTH FATTY ACIDS, GLYCERIDES AND ANALOGUES AS NEUTROPHIL SURVIVAL AND ACTIVATION FACTORS PROMETIC BIOSCIENCES INC. (CA) 2002-10-24 — — WO disclosed
EP-0969828-B1 BUTYRATE PRODRUGS DERIVED FROM LACTIC ACID VERTEX PHARMA (US) 2002-09-04 — — EP disclosed
US-20020115716-A1 Prodrug, salt or analogue of butyrate sufficient to maintain a serum butyrate concentration of between 10 and 200 mu M for 1 to 8 consecutive hours CHATURVEDI PRAVIN (US) 2002-08-22 — — US disclosed
EP-1162884-A4 ORAL LOW DOSE BUTYRATE COMPOSITIONS VERTEX PHARMA (US) 2002-07-24 — — EP disclosed
EP-1162884-A1 ORAL LOW DOSE BUTYRATE COMPOSITIONS Vertex Pharmaceuticals Incorporated (US) 2001-12-19 — — EP disclosed
US-6225350-B1 ADMINISTERING BUTYRATE PRODRUG FOR THERAPY OF CYSTIC FIBROSIS VERTEX PHARMACEUTICALS, INC. 2001-05-01 — — US disclosed
WO-2000056153-A1 ORAL LOW DOSE BUTYRATE COMPOSITIONS VERTEX PHARMACEUTICALS INCORPORATED (US) 2000-09-28 — — WO disclosed
EP-0969828-A1 BUTYRATE PRODRUGS DERIVED FROM LACTIC ACID Vertex Pharmaceuticals Incorporated (US) 2000-01-12 — — EP disclosed
US-5880152-A INFLAMMATORY BOWEL DISEASE VERTEX PHARMACEUTICALS, INC. (US) 1999-03-09 — — US disclosed
WO-1998040064-A1 BUTYRATE PRODRUGS DERIVED FROM LACTIC ACID VERTEX PHARMACEUTICALS INCORPORATED (US) 1998-09-17 — — 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 (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-20180162799-A1 SUBSTITUTED AROMATIC COMPOUNDS AND PHARMACEUTICAL USES THEREOF TYR, PAH, REN LMNA 2244/4885SMN1; SMN2 3758/4885ALDH1A1 190/4885
US-10815183-B2 Substituted aromatic compounds and pharmaceutical uses thereof TYR, PAH, REN LMNA 2244/4885SMN1; SMN2 3758/4885ALDH1A1 190/4885
US-20210002202-A1 Substituted Aromatic Compounds and Pharmaceutical Uses Thereof TYR, PAH, REN LMNA 2244/4885SMN1; SMN2 3758/4885ALDH1A1 190/4885

“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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