SCHEMBL6567531

SCHEMBL6567531

CCOC(=O)CC(=O)COCc1ccc(C)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 3/20 0.48
HSD17B10 Q99714 1/20 0.48
RAB9A P51151 4/20 0.46
NPC1 O15118 2/20 0.46
MGAM O43451 1/20 0.42
SI P14410 1/20 0.42
MGAM2 Q2M2H8 1/20 0.42
HTT P42858 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
NLRP3 Q96P20 1/20 0.41
HRH3 Q9Y5N1 1/20 0.41
CYP4F2 P78329 1/20 0.41
CYP4A11 Q02928 1/20 0.41
MAPT P10636 3/20 0.40
CYP1A2 P05177 1/20 0.40
CYP2C19 P33261 1/20 0.40
ALDH1A1 P00352 1/20 0.39
MAPK1 P28482 1/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 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
SCHEMBL6565313 0.91 ALDH1A1 (0.43) GAAHSD17B10MGAMSIMGAM2
SCHEMBL53331 0.88 PPID (0.49) GAAHSD17B10RAB9ANPC1MGAM
SCHEMBL6568404 0.87 RAB9A (0.49) RAB9ANPC1MAPTCYP1A2CYP2C19
SCHEMBL130309 0.87 KMT2A (0.49) RAB9ANPC1HTTSMN1; SMN2MAPT
SCHEMBL2042795 0.85 PPID (0.47) GAAHSD17B10RAB9ANPC1SMN1; SMN2
SCHEMBL3230548 0.80 LMNA (0.47) SMN1; SMN2ALDH1A1MEN1KMT2A
SCHEMBL15334365 0.80 GAA (0.52) GAAHSD17B10MGAMSIMGAM2
SCHEMBL29105138 0.78 RAB9A (0.53) RAB9ANPC1MAPTCYP1A2CYP2C19
SCHEMBL7231280 0.78 ALDH1A1 (0.45) GAAHSD17B10RAB9ANPC1SMN1; SMN2
SCHEMBL10468620 0.77 HSD11B1 (0.51) GAAHSD17B10MAPTCYP1A2CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1277748-B1 Process for producing optically active y-Butyrolactone TAKASAGO PERFUMERY CO LTD (JP) 2004-04-21 EP disclosed
EP-1403262-A1 Process for producing optically active alpha butyrolactone Takasago International Corporation (JP) 2004-03-31 EP disclosed
US-6608214-B2 Hydrogenating optically active 4-substituted oxy-3-hydroxy-butyrate followed by simultaneous deprotection and ring closure; economic and efficient synthesis TAKASAGO INTERNATIONAL CORPORATION (JP) 2003-08-19 US disclosed
US-20030105341-A1 Process for producing optically active gamma-butyrolactone TAKASAGO INTERNATIONAL CORPORATION (JP) 2003-06-05 US disclosed
EP-1277748-A1 Process for producing optically active y-Butyrolactone Takasago International Corporation (JP) 2003-01-22 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 (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-20030105341-A1 Process for producing optically active gamma-butyrolactone HSD17B10, HSD17B1, HSD17B12 GAA 1376/4885HSD17B10 1/4885RAB9A 4454/4885

“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.