SCHEMBL5085693

SCHEMBL5085693

C[C@@H](O)CCCCc1nc2c(c(=O)[nH]c(=O)n2C)n1C

nearest known ligand 0.49

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 3/20 0.49
▸ GAA P10253 1/20 0.49
▸ HSD17B10 Q99714 5/20 0.47
▸ SMN1; SMN2 Q16637 2/20 0.45
▸ ALDH1A1 P00352 7/20 0.45
▸ HPGD P15428 3/20 0.45
▸ KDM4E B2RXH2 2/20 0.44
▸ TSHR P16473 3/20 0.43
▸ ALOX15 P16050 1/20 0.43
▸ MAPK1 P28482 1/20 0.43
▸ GFER P55789 1/20 0.43
▸ MEN1 O00255 1/20 0.43
▸ KMT2A Q03164 1/20 0.43
▸ NPSR1 Q6W5P4 2/20 0.42
▸ MAPT P10636 1/20 0.42
▸ HTT P42858 1/20 0.42
▸ POLB P06746 1/20 0.42
▸ ATM Q13315 1/20 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
SCHEMBL4749492 1.00 L3MBTL1 (0.49) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL1495136 1.00 L3MBTL1 (0.49) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952697 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952567 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952590 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952589 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952565 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952580 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952600 0.99 L3MBTL1 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL8952621 0.88 HSD17B10 (0.48) L3MBTL1GAAHSD17B10SMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1999033468-A9 METHOD FOR TREATING HYPEROXIA CELL THERAPEUTICS INC (US) 1999-09-23 — — WO claimed
WO-1999033468-A1 METHOD FOR TREATING HYPEROXIA CELL THERAPEUTICS, INC. (US) 1999-07-08 — — WO claimed
EP-0584347-A4 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS. CELL THERAPEUTICS INC (US) 1995-04-26 — — EP claimed
EP-0584347-A1 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS CELL THERAPEUTICS, INC. (US) 1994-03-02 — — EP claimed
WO-1993017684-A2 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS CELL THERAPEUTICS, INC. (US) 1993-09-16 — — WO claimed
WO-2008033754-A2 XANTHINE DERIVATIVES IN METHODS AND COMPOSITIONS FOR THE TREATMENT OF VASCULAR DEPRESSION DUKE UNIVERSITY (US) 2008-03-20 — — WO disclosed
EP-0584347-B1 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS CELL THERAPEUTICS INC (US) 2003-01-15 — — EP disclosed
EP-0988372-A4 MAMMALIAN LYSOPHOSPHATIDIC ACID ACYLTRANSFERASE CELL THERAPEUTICS INC (US) 2003-01-02 — — EP disclosed
EP-0759915-B1 ASYMMETRIC SYNTHESIS OF CHIRAL SECONDARY ALCOHOLS CELL THERAPEUTICS INC (US) 2002-10-16 — — EP disclosed
EP-0988372-A1 MAMMALIAN LYSOPHOSPHATIDIC ACID ACYLTRANSFERASE CELL THERAPEUTICS, INC. (US) 2000-03-29 — — EP disclosed
US-5965564-A TREATING OR PREVENTING INFECTION FOLLOWING TREATMENT FOR HEMATOLOGIC MALIGNANCY SUCH AS CHEMOTHERAPY, BY ADMINISTERING A XANTHINE DERIVATIVE WHICH IS 1-SUBSTITUTED WITH AN R ENANTIOMER OMEGA-1 SECONDARY ALCOHOL-SUBSTITUTED ALKYL GROUP CELL THERAPEUTICS, INC. (US) 1999-10-12 — — US disclosed
WO-1999033468-A9 METHOD FOR TREATING HYPEROXIA CELL THERAPEUTICS INC (US) 1999-09-23 — — WO disclosed
WO-1995031450-A1 ASYMMETRIC SYNTHESIS OF CHIRAL SECONDARY ALCOHOLS CELL THERAPEUTICS, INC. (US) 1995-11-23 — — WO disclosed
EP-0676958-A1 METHOD FOR INHIBITING INTRACELLULAR VIRAL REPLICATION CELL THERAPEUTICS, INC. (US) 1995-10-18 — — EP disclosed
WO-1995024199-A2 USE OF COMPOUNDS WHICH INHIBIT PHOSPHATIDIC ACID FORMATION FOR THE MANUFACTURE OF A MEDICAMENT FOR THE TREATMENT OF CANCER CELL THERAPEUTICS, INC. (US) 1995-09-14 — — WO disclosed
WO-1995013075-A1 METHOD FOR PREVENTING TISSUE INJURY FROM HYPOXIA CELL THERAPEUTICS, INC. (US) 1995-05-18 — — WO disclosed
WO-1995012396-A1 METHOD FOR INHIBITING INTRACELLULAR VIRAL REPLICATION CELL THERAPEUTICS, INC. (US) 1995-05-11 — — WO disclosed
EP-0584347-A4 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS. CELL THERAPEUTICS INC (US) 1995-04-26 — — EP disclosed
EP-0584347-A1 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS CELL THERAPEUTICS, INC. (US) 1994-03-02 — — EP disclosed
WO-1993017684-A2 ENANTIOMERIC HYDROXYLATED XANTHINE COMPOUNDS CELL THERAPEUTICS, INC. (US) 1993-09-16 — — WO disclosed
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