SCHEMBL203576

SCHEMBL203576

CCCc1ccc(-c2ccc(C(=O)N[C@@H](CCSC)C(=O)NO)cc2)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.56
TAS1R3 Q7RTX0 1/20 0.51
TAS1R1 Q7RTX1 1/20 0.51
CTSB P07858 1/20 0.49
ANPEP P15144 1/20 0.49
ALDH1A1 P00352 2/20 0.47
MEN1 O00255 1/20 0.47
CRHBP P24387 1/20 0.47
KMT2A Q03164 1/20 0.47
CRHR2 Q13324 1/20 0.47
CA2 P00918 3/20 0.47
CA1 P00915 2/20 0.47
CA12 O43570 2/20 0.47
CA9 Q16790 2/20 0.47
PLK1 P53350 1/20 0.45
NPC1 O15118 1/20 0.44
RAB9A P51151 1/20 0.44
POLB P06746 1/20 0.44
CTDSP1 Q9GZU7 1/20 0.44
USP2 O75604 1/20 0.43

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
SCHEMBL203577 1.00 L3MBTL1 (0.56) L3MBTL1TAS1R3TAS1R1CTSBANPEP
SCHEMBL201120 0.89 TAS1R3 (0.54) L3MBTL1TAS1R3TAS1R1CTSBANPEP
SCHEMBL2692851 0.89 TAS1R3 (0.54) L3MBTL1TAS1R3TAS1R1CTSBANPEP
SCHEMBL201119 0.89 TAS1R3 (0.54) L3MBTL1TAS1R3TAS1R1CTSBANPEP
SCHEMBL201285 0.88 CA2 (0.60) L3MBTL1TAS1R3TAS1R1CTSBALDH1A1
SCHEMBL201891 0.86 L3MBTL1 (0.76) L3MBTL1TAS1R3TAS1R1KMT2ACA2
SCHEMBL201908 0.86 L3MBTL1 (0.76) L3MBTL1TAS1R3TAS1R1KMT2ACA2
SCHEMBL404117 0.84 TAS1R3 (0.56) L3MBTL1TAS1R3TAS1R1CTSBANPEP
SCHEMBL200992 0.84 TAS1R3 (0.51) L3MBTL1TAS1R3TAS1R1ALDH1A1PLK1
SCHEMBL2692848 0.84 TAS1R3 (0.51) L3MBTL1TAS1R3TAS1R1ALDH1A1PLK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8088804-B2 N-hydroxyamide derivatives possessing antibacterial activity PFIZER INC. (US) 2012-01-03 US disclosed
US-8088804-B2 N-hydroxyamide derivatives possessing antibacterial activity PFIZER INC. (US) 2012-01-03 US disclosed
US-8088804-B2 N-hydroxyamide derivatives possessing antibacterial activity PFIZER INC. (US) 2012-01-03 US disclosed
EP-2338878-A2 N-hydroxyamide derivatives possessing antibacterial activity Vicuron Pharmaceuticals, Inc. (US) 2011-06-29 EP disclosed
US-20100022605-A1 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS INC. 2010-01-28 US disclosed
US-20100022605-A1 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS INC. 2010-01-28 US disclosed
US-20100022605-A1 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS INC. 2010-01-28 US disclosed
EP-1963262-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY Vicuron Pharmaceuticals, Inc. (US) 2008-09-03 EP disclosed
WO-2007069020-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS INC. (US) 2007-06-21 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-20100022605-A1 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY NAAA, HDHD5, HACL2 L3MBTL1 2179/4885TAS1R3 1250/4885TAS1R1 1011/4885

“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.