SCHEMBL25400409

SCHEMBL25400409

O=C(ON1C(=O)CCC1=O)[C@@H]1CCCN1C(=O)OCC1c2ccccc2-c2ccccc21

nearest known ligand 0.41

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ KLK7 P49862 1/20 0.41
▸ KLK5 Q9Y337 1/20 0.41
▸ F2 P00734 2/20 0.39
▸ ALDH1A1 P00352 2/20 0.39
▸ SMN1; SMN2 Q16637 1/20 0.39
▸ FABP5 Q01469 3/20 0.38
▸ FABP7 O15540 2/20 0.38
▸ PREP P48147 3/20 0.37
▸ FKBP1A P62942 2/20 0.37
▸ KMT2A Q03164 1/20 0.37
▸ CTSK P43235 1/20 0.36
▸ CTRB1 P17538 1/20 0.36
▸ TSHR P16473 1/20 0.36

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
SCHEMBL29398515 1.00 KLK7 (0.41) KLK7KLK5F2ALDH1A1SMN1; SMN2
SCHEMBL25400415 1.00 KLK7 (0.41) KLK7KLK5F2ALDH1A1SMN1; SMN2
SCHEMBL31603928 0.85 KMT2A (0.46) F2FKBP1AKMT2A
SCHEMBL29384614 0.84 ALDH1A1 (0.43) KLK7KLK5F2ALDH1A1SMN1; SMN2
SCHEMBL15083158 0.83 PDK2 (0.45) F2ALDH1A1SMN1; SMN2FABP5FABP7
SCHEMBL15803221 0.83 PDK2 (0.45) F2ALDH1A1SMN1; SMN2FABP5FABP7
SCHEMBL14417972 0.82 ALDH1A1 (0.46) F2ALDH1A1SMN1; SMN2FKBP1AKMT2A
SCHEMBL1002927 0.82 ALDH1A1 (0.58) F2ALDH1A1SMN1; SMN2FABP5FABP7
SCHEMBL118354 0.82 ALDH1A1 (0.58) F2ALDH1A1SMN1; SMN2FABP5FABP7
SCHEMBL119560 0.82 ALDH1A1 (0.58) F2ALDH1A1SMN1; SMN2FABP5FABP7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110183532-B Process method for synthesizing bivalirudin protected pentapeptide fragments by mass high-efficiency liquid phase method 济南爱思医药科技有限公司 2023-06-30 — — CN claimed
CN-110183532-A A kind of high-volume high-efficient liquid phase technique synthesis bivalirudin protects the process of five peptide fragments 济南爱思医药科技有限公司 2019-08-30 — — CN claimed
US-20230293716-A1 ELASTASE-SUBSTRATE, PEPTIDE LINKER IMMUNOCONJUGATES, AND USES THEREOF BOLT BIOTHERAPEUTICS, INC. (US) 2023-09-21 — — US disclosed
US-20230293716-A1 ELASTASE-SUBSTRATE, PEPTIDE LINKER IMMUNOCONJUGATES, AND USES THEREOF BOLT BIOTHERAPEUTICS, INC. (US) 2023-09-21 — — US disclosed
CN-110183532-B Process method for synthesizing bivalirudin protected pentapeptide fragments by mass high-efficiency liquid phase method 济南爱思医药科技有限公司 2023-06-30 — — CN disclosed
CN-115996756-A Elastase substrate peptide linker immunoconjugates and uses thereof 博尔特生物治疗药物有限公司 2023-04-21 — — CN disclosed
CN-110183532-A A kind of high-volume high-efficient liquid phase technique synthesis bivalirudin protects the process of five peptide fragments 济南爱思医药科技有限公司 2019-08-30 — — CN 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-20230293716-A1 ELASTASE-SUBSTRATE, PEPTIDE LINKER IMMUNOCONJUGATES, AND USES THEREOF SERPINB1, ELANE, CELA1 KLK7 102/4885KLK5 144/4885F2 469/4885

“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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