SCHEMBL10144173

SCHEMBL10144173

CCOC(=O)[C@@H](NC(=O)[C@H](CCC(C)=O)NC(=O)OC(C)(C)C)C(C)C

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ CYP1A2 P05177 1/20 0.48
▸ CYP2C9 P11712 1/20 0.48
▸ CYP2C19 P33261 1/20 0.48
▸ HTT P42858 1/20 0.48
▸ CTSK P43235 6/20 0.43
▸ CTSS P25774 5/20 0.43
▸ ALDH1A1 P00352 2/20 0.43
▸ MAPT P10636 2/20 0.43
▸ SMN1; SMN2 Q16637 1/20 0.42
▸ REN P00797 1/20 0.40
▸ CTSD P07339 1/20 0.40
▸ PSENEN Q9NZ42 1/20 0.39
▸ CAPN1 P07384 1/20 0.39
▸ CA1 P00915 1/20 0.39
▸ CA2 P00918 1/20 0.39
▸ CA7 P43166 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
SCHEMBL16383458 0.90 CYP1A2 (0.51) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL10144106 0.90 PSENEN (0.45) CTSKCTSSRENCTSDPSENEN
SCHEMBL10144064 0.84 CTSS (0.57) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL14914482 0.84 CYP1A2 (0.60) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL21873981 0.84 CYP1A2 (0.60) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL2463121 0.84 CYP1A2 (0.60) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL13956771 0.81 CTSK (0.55) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL2721327 0.81 CTSK (0.55) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL20052432 0.81 CYP1A2 (0.49) CYP1A2CYP2C9CYP2C19HTTCTSK
SCHEMBL30698104 0.80 CTSS (0.49) CYP1A2CYP2C9CYP2C19HTTCTSK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9382193-B2 Processes for forming amide bonds and compositions related thereto EMORY UNIVERSITY (US) 2016-07-05 — — US disclosed
US-20150315129-A1 PROCESSES FOR FORMING AMIDE BONDS AND COMPOSITIONS RELATED THERETO NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2015-11-05 — — US disclosed
US-8921599-B2 Processes for forming amide bonds and compositions related thereto EMORY UNIVERSITY (US) 2014-12-30 — — US disclosed
US-20120107902-A1 Processes For Forming Amide Bonds And Compositions Related Thereto EMORY UNIVERSITY (US) 2012-05-03 — — 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 (2 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-20150315129-A1 PROCESSES FOR FORMING AMIDE BONDS AND COMPOSITIONS RELATED THERETO TMT1A, LPO, GSTO1 CYP1A2 1938/4885CYP2C9 1394/4885CYP2C19 2688/4885
US-20120107902-A1 Processes For Forming Amide Bonds And Compositions Related Thereto TMT1A, LPO, GSTO1 CYP1A2 1938/4885CYP2C9 1394/4885CYP2C19 2688/4885

“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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