SCHEMBL84538

SCHEMBL84538

COC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCc1ccccc1)NC(=O)OC(C)(C)C

nearest known ligand 0.62

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
REN P00797 8/20 0.62
CTSS P25774 1/20 0.59
CTSK P43235 1/20 0.59
PSEN1 P49768 6/20 0.55
PSEN2 P49810 6/20 0.55
APH1B Q8WW43 6/20 0.55
NCSTN Q92542 6/20 0.55
APH1A Q96BI3 6/20 0.55
PSENEN Q9NZ42 6/20 0.55
KLK5 Q9Y337 1/20 0.55
CAPN1 P07384 1/20 0.55
CTSD P07339 1/20 0.53

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
SCHEMBL30485406 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL8080979 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL28377172 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL28373438 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL28372334 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL30485379 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL28372331 1.00 REN (0.62) RENCTSSCTSKPSEN1PSEN2
SCHEMBL17452195 0.94 CTSS (0.63) RENCTSSCTSKPSEN1PSEN2
SCHEMBL8073093 0.94 REN (0.68) RENCTSSCTSKPSEN1PSEN2
SCHEMBL18171935 0.94 REN (0.68) RENCTSSCTSKPSEN1PSEN2

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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117683080-A Synthesis method of carfilzomib key intermediate 湖南华腾制药有限公司 2024-03-12 CN disclosed
CN-117683080-A Synthesis method of carfilzomib key intermediate 湖南华腾制药有限公司 2024-03-12 CN disclosed
CN-110964085-B Preparation method of carfilzomib and derivatives thereof 扬子江药业集团有限公司 2023-07-07 CN disclosed
EP-3297678-B1 AN IMPROVED PROCESSES FOR THE PREPARATION OF CARFILZOMIB OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF LAURUS LABS LTD (IN) 2021-07-07 EP disclosed
US-10800809-B2 Processes for the preparation of carfilzomib or pharmaceutically acceptable salts thereof LAURUS LABS LIMITED (IN) 2020-10-13 US disclosed
CN-110964085-A Preparation method of carfilzomib and derivatives thereof 扬子江药业集团有限公司 2020-04-07 CN disclosed
US-10544189-B2 Process for the preparation of (2S)-N-((S)-1-((S)-4-methyl-1-((R)-2-methyl oxiran-2-yl)-1-oxopentan-2-ylcarbamoyl)-2-phenylethyl)-2-((S)-2-(2-morpholinoacetamido)-4-phenylbutanamido)-4-methylpentanamide MSN LABORATORIES PRIVATE LIMITED (IN) 2020-01-28 US disclosed
US-20190284231-A1 PROCESSES FOR THE PREPARATION OF CARFILZOMIB OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF LAURUS LABS LIMITED (IN) 2019-09-19 US disclosed
US-10364269-B2 Processes for the preparation of carfilzomib or pharmaceutically acceptable salts thereof LAURUS LABS LIMITED (IN) 2019-07-30 US disclosed
US-10253066-B2 Process for purification of Carfilzomib FRESENIUS KABI ONCOLOGY LIMITED (IN) 2019-04-09 US disclosed
EP-2207791-B1 CRYSTALLINE PEPTIDE EPOXY KETONE PROTEASE INHIBITORS AND THE SYNTHESIS OF AMINO ACID KETO-EPOXIDES ONYX THERAPEUTICS INC (US) 2016-04-13 EP disclosed
US-8129346-B2 Compounds for enzyme inhibition ONYX THERAPEUTICS, INC. (US) 2012-03-06 US disclosed
US-20090215093-A1 COMPOUNDS FOR ENZYME INHIBITION PROTEOLIX, INC. (US) 2009-08-27 US disclosed
US-20090215093-A1 COMPOUNDS FOR ENZYME INHIBITION PROTEOLIX, INC. (US) 2009-08-27 US disclosed
US-20090105156-A1 Crystalline peptide epoxy ketone protease inhibitors and the synthesis of amino acid keto-epoxides PROTEOLIX, INC. (US) 2009-04-23 US disclosed
US-7491704-B2 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2009-02-17 US disclosed
US-20080200398-A1 Compounds For Enzyme Inhibition PROTEOLIX, INC. (US) 2008-08-21 US disclosed
US-20070191284-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2007-08-16 US disclosed
US-7232818-B2 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2007-06-19 US disclosed
WO-2005105827-A2 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. (US) 2005-11-10 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 (8 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-10544189-B2 Process for the preparation of (2S)-N-((S)-1-((S)-4-methyl-1-((R)-2-methyl oxiran-2-yl)-1-oxopentan-2-ylcarbamoyl)-2-phenylethyl)-2-((S)-2-(2-morpholinoacetamido)-4-phenylbutanamido)-4-methylpentanamide OPRL1, PNMT, HTR1A REN 853/4885CTSS 3195/4885CTSK 4479/4885
US-10364269-B2 Processes for the preparation of carfilzomib or pharmaceutically acceptable salts thereof SF3B5, PRCP, GBA1 REN 17/4885CTSS 132/4885CTSK 252/4885
US-10800809-B2 Processes for the preparation of carfilzomib or pharmaceutically acceptable salts thereof SF3B5, PRCP, GBA1 REN 17/4885CTSS 132/4885CTSK 252/4885
US-20080200398-A1 Compounds For Enzyme Inhibition ANPEP, DNPEP, CPN1 REN 592/4885CTSS 70/4885CTSK 92/4885
US-10253066-B2 Process for purification of Carfilzomib PSMB5, PSMA5, PSMB2 REN 60/4885CTSS 923/4885CTSK 894/4885
US-20190284231-A1 PROCESSES FOR THE PREPARATION OF CARFILZOMIB OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF SF3B5, PRCP, GBA1 REN 17/4885CTSS 132/4885CTSK 252/4885
US-20070191284-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents ANPEP, DNPEP, PSMB1 REN 826/4885CTSS 100/4885CTSK 128/4885
US-20090105156-A1 Crystalline peptide epoxy ketone protease inhibitors and the synthesis of amino acid keto-epoxides PREP, ANPEP, DNPEP REN 36/4885CTSS 31/4885CTSK 37/4885

“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.