SCHEMBL7144545

SCHEMBL7144545

COC(OC)(C(O)CNC(=O)c1ccccc1)C(c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 3/20 0.49
NPC1 O15118 2/20 0.49
SMN1; SMN2 Q16637 2/20 0.49
PRSS1 P07477 1/20 0.43
CTSG P08311 1/20 0.43
CTRB1 P17538 1/20 0.43
CMA1 P23946 1/20 0.43
HPGD P15428 1/20 0.43
GAA P10253 2/20 0.42
NAAA Q02083 1/20 0.41
ITGAV P06756 1/20 0.41
CES1 P23141 1/20 0.41
ESRRG P62508 1/20 0.41
LMNA P02545 2/20 0.40
KMT2A Q03164 2/20 0.40
TSHR P16473 1/20 0.40
BACE1 P56817 1/20 0.40
HSD17B10 Q99714 1/20 0.40
POLB P06746 1/20 0.40
ALDH1A1 P00352 1/20 0.39

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
SCHEMBL8041093 0.73 NPC1 (0.60) RAB9ANPC1SMN1; SMN2PRSS1CTSG
SCHEMBL7145599 0.73 KIF11 (0.38) CES1ALDH1A1
SCHEMBL3601229 0.71 KMT2A (0.68) RAB9ANPC1SMN1; SMN2PRSS1CTSG
SCHEMBL8506869 0.71 NPC1 (0.66) RAB9ANPC1SMN1; SMN2HPGDGAA
SCHEMBL8507006 0.71 NPC1 (0.66) RAB9ANPC1SMN1; SMN2HPGDGAA
SCHEMBL3377096 0.71 NPC1 (0.66) RAB9ANPC1SMN1; SMN2HPGDGAA
SCHEMBL7561649 0.70 NPC1 (0.70) RAB9ANPC1SMN1; SMN2PRSS1CTSG
SCHEMBL18680060 0.70 SMN1; SMN2 (0.56) RAB9ANPC1SMN1; SMN2PRSS1CTSG
SCHEMBL7121699 0.70 RAB9A (0.59) RAB9ANPC1SMN1; SMN2HPGDGAA
SCHEMBL255251 0.69 GAA (0.76) RAB9ANPC1SMN1; SMN2HPGDGAA

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030065146-A1 Monomeric diols, phosphate linked oligomers formed therefrom and processes for preparing COOK PHILLIP D (US) 2003-04-03 US disclosed
US-6448373-B1 INHIBITORS OF ENZYMES SUCH AS PHOSPHOLIPASE A2; TREATMENT OF INFLAMMATORY DISEASES INCLUDING ATOPIC DERMATITIS AND INFLAMMATORY BOWEL DISEASE ISIS PHARMACEUTICALS, INC. 2002-09-10 US disclosed
EP-0739351-B1 MONOMERIC DIOLS AND PHOSPHATE LINKED OLIGOMERS FORMED THEREFROM ISIS PHARMACEUTICALS INC (US) 2002-04-10 EP disclosed
US-5886177-A ETHYLENE GLYCOL MONOMERS JOINED VIA STANDARD PHOSPHATE LINKAGES INCLUDING PHOSPHOROTHIOATE, PHOSPHODIESTER, AND PHOSPHORAMIDATE LINKAGES; USEFUL FUNCTIONAL GROUPS INCLUDE NUCLEOBASES AS WELL AS POLAR GROUPS, HYDROPHOBIC GROUPS ISIS PHARMACEUTICALS, INC. (US) 1999-03-23 US disclosed
EP-0739351-A4 MONOMERIC DIOLS AND PHOSPHATE LINKED OLIGOMERS FORMED THEREFROM ISIS PHARMACEUTICALS INC (US) 1998-10-21 EP disclosed
EP-0739351-A1 MONOMERIC DIOLS AND PHOSPHATE LINKED OLIGOMERS FORMED THEREFROM ISIS PHARMACEUTICALS, INC. (US) 1996-10-30 EP disclosed
WO-1995018820-A1 MONOMERIC DIOLS AND PHOSPHATE LINKED OLIGOMERS FORMED THEREFROM ISIS PHARMACEUTICALS, INC. (US) 1995-07-13 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 (1 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-20030065146-A1 Monomeric diols, phosphate linked oligomers formed therefrom and processes for preparing BPGM, PPIP5K2, PGM2 RAB9A 4371/4885NPC1 4306/4885SMN1; SMN2 3732/4885

“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.