SCHEMBL6359073

SCHEMBL6359073

Cc1cccc(CC(=O)c2cccc(C)c2)c1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CTBP2 P56545 1/20 0.54
▸ PARP1 P09874 1/20 0.53
▸ POLB P06746 1/20 0.53
▸ CTNNB1 P35222 2/20 0.50
▸ WNT3A P56704 2/20 0.50
▸ NPC1 O15118 1/20 0.50
▸ RAB9A P51151 1/20 0.50
▸ HDAC8 Q9BY41 1/20 0.50
▸ HDAC6 Q9UBN7 1/20 0.50
▸ HPGD P15428 1/20 0.50
▸ TDP1 Q9NUW8 1/20 0.50
▸ L3MBTL1 Q9Y468 1/20 0.49
▸ MAOB P27338 1/20 0.49
▸ GPR52 Q9Y2T5 1/20 0.48
▸ MEN1 O00255 1/20 0.48
▸ FFAR1 O14842 1/20 0.48
▸ TP53 P04637 1/20 0.48
▸ GLA P06280 1/20 0.48
▸ KMT2A Q03164 1/20 0.48
▸ SMN1; SMN2 Q16637 1/20 0.47

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
SCHEMBL165944 0.91 CTBP2 (0.57) CTBP2POLBNPC1RAB9ATDP1
SCHEMBL3289372 0.91 L3MBTL1 (0.58) PARP1POLBCTNNB1WNT3ANPC1
SCHEMBL3280980 0.89 KCNK3 (0.51) CTBP2PARP1POLBNPC1RAB9A
SCHEMBL3283011 0.89 KCNK3 (0.51) CTBP2PARP1CTNNB1WNT3ANPC1
SCHEMBL2477387 0.87 NPC1 (0.57) CTBP2POLBNPC1RAB9AL3MBTL1
SCHEMBL11382971 0.87 RAB9A (0.57) PARP1CTNNB1WNT3ANPC1RAB9A
SCHEMBL25760942 0.86 CTBP2 (0.49) CTBP2POLBNPC1RAB9ATDP1
SCHEMBL9315993 0.86 RAF1 (0.56) CTBP2POLBHDAC6HPGDTDP1
SCHEMBL18214571 0.86 KCNK3 (0.53) CTBP2PARP1CTNNB1WNT3AHPGD
SCHEMBL16171153 0.86 MEN1 (0.52) PARP1CTNNB1WNT3ANPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10000443-B2 Compositions and methods for glucose transport inhibition OHIO UNIVERSITY (US) 2018-06-19 — — US disclosed
US-20160137585-A1 COMPOSITIONS AND METHODS FOR GLUCOSE TRANSPORT INHIBITION OHIO UNIVERSITY (US) 2016-05-19 — — US disclosed
US-9181162-B2 Compositions and methods for glucose transport inhibition OHIO UNIVERSITY (US) 2015-11-10 — — US disclosed
US-8357210-B2 Disazo acid dyes CLARIANT FINANCE (BVI) LIMITED (VG) 2013-01-22 — — US disclosed
US-20120121536-A1 COMPOSITIONS AND METHODS FOR GLUCOSE TRANSPORT INHIBITION OHIO UNIVERSITY (US) 2012-05-17 — — US disclosed
US-20110203058-A1 Disazo Acid Dyes CLARIANT FINANCE (BVI) LIMITED (VG) 2011-08-25 — — 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 (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-20160137585-A1 COMPOSITIONS AND METHODS FOR GLUCOSE TRANSPORT INHIBITION SLC2A1, SLC2A4, SLC2A3 CTBP2 782/4885PARP1 2679/4885POLB 3378/4885
US-20120121536-A1 COMPOSITIONS AND METHODS FOR GLUCOSE TRANSPORT INHIBITION SLC2A1, SLC2A4, SLC2A3 CTBP2 782/4885PARP1 2679/4885POLB 3378/4885
US-10000443-B2 Compositions and methods for glucose transport inhibition SLC2A1, SLC2A4, SLC2A3 CTBP2 782/4885PARP1 2679/4885POLB 3378/4885

“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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