SCHEMBL1219335

SCHEMBL1219335

O=CC1CCCN1C(=O)C1CCCN1

nearest known ligand 0.59

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ DPP4 P27487 16/20 0.59
▸ DPP8 Q6V1X1 6/20 0.59
▸ DPP9 Q86TI2 4/20 0.59
▸ FAP Q12884 1/20 0.59
▸ DPP7 Q9UHL4 1/20 0.59
▸ ANPEP P15144 1/20 0.44

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
SCHEMBL30511428 1.00 DPP4 (0.59) DPP4DPP8DPP9FAPDPP7
SCHEMBL1695702 0.86 DPP4 (0.46) DPP4DPP8DPP9FAPDPP7
SCHEMBL21226746 0.77 DPP4 (0.59) DPP4DPP8DPP9FAPDPP7
SCHEMBL28054657 0.77 DPP4 (0.55) DPP4DPP8DPP9FAPDPP7
SCHEMBL28054834 0.77 DPP4 (0.55) DPP4DPP8DPP9FAPDPP7
SCHEMBL1798265 0.77 DPP4 (0.62) DPP4DPP8DPP9FAPDPP7
SCHEMBL16307729 0.77 DPP4 (0.62) DPP4DPP8DPP9FAPDPP7
SCHEMBL1798266 0.77 DPP4 (0.62) DPP4DPP8DPP9FAPDPP7
SCHEMBL30924754 0.75 DPP4 (0.60) DPP4DPP8DPP9FAPDPP7
SCHEMBL6371844 0.75 DPP4 (0.60) DPP4DPP8DPP9FAPDPP7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240100018-A1 COMPOUNDS FOR THE TREATMENT OF A DISEASE OR DISORDER, METHODS FOR IDENTIFYING SAID COMPOUNDS CEDARS-SINAI MEDICAL CENTER 2024-03-28 — — US disclosed
US-20230218577-A1 USE OF HEAT SHOCK PROTEIN INHIBITORS FOR THE TREATMENT OF NEURODEVELOPMENTAL DISORDERS THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2023-07-13 — — US disclosed
US-10584313-B2 Method of producing a differentiated mammalian cell comprising culturing a single mammalian blastomere ASTELLAS INSTITUTE FOR REGENERATIVE MEDICINE (US) 2020-03-10 — — US disclosed
US-10072243-B2 Derivation of embryonic stem cells and embryo-derived cells ASTELLAS INSTITUTE FOR REGENERATIVE MEDICINE (US) 2018-09-11 — — US disclosed
US-20170240857-A1 DERIVATION OF EMBRYONIC STEM CELLS AND EMBRYO-DERIVED CELLS ADVANCED CELL TECHNOLOGY, INC. 2017-08-24 — — US disclosed
EP-3190178-A1 HIGHLY EFFICIENT METHODS FOR REPROGRAMMING DIFFERENTIATED CELLS AND FOR GENERATING ANIMALS AND EMBRYONIC STEM CELLS FROM REPROGRAMMED CELLS Astellas Institute for Regenerative Medicine (US) 2017-07-12 — — EP disclosed
US-9617512-B2 Derivation of embryonic stem cells and embryo-derived cells ASTELLAS INSTITUTE FOR REGENERATIVE MEDICINE (US) 2017-04-11 — — US disclosed
EP-3133150-A2 DERIVATION OF EMBRYONIC STEM CELLS AND EMBRYO-DERIVED CELLS Astellas Institute for Regenerative Medicine (US) 2017-02-22 — — EP disclosed
US-20160369237-A1 METHODS TO ACCELERATE THE ISOLATION OF NOVEL CELL STRAINS FROM PLURIPOTENT STEM CELLS AND CELLS OBTAINED THEREBY ADVANCED CELL TECH INC (US) 2016-12-22 — — US disclosed
EP-2982744-A1 HIGHLY EFFICIENT METHODS FOR REPROGRAMMING DIFFERENTIATED CELLS AND FOR GENERATING ANIMALS AND EMBRYONIC STEM CELLS FROM REPROGRAMMED CELLS Advanced Cell Technology, Inc. (US) 2016-02-10 — — EP disclosed
EP-2029724-A2 DERIVATION OF EMBRYONIC STEM CELLS AND EMBRYO-DERIVED CELLS Advanced Cell Technology, Inc. (US) 2009-03-04 — — EP disclosed
WO-2008103462-A2 HIGHLY EFFICIENT METHODS FOR REPROGRAMMING DIFFERENTIATED CELLS AND FOR GENERATING ANIMALS AND EMBRYONIC STEM CELLS FROM REPROGRAMMED CELLS ADVANCED CELL TECHNOLOGY, INC. (US) 2008-08-28 — — WO disclosed
US-20080070303-A1 Using myocardial and/or muscle progenitor cells as modeling tool in tissue engineering; regenerative medicine and organ replacement ADVANCED CELL TECHNOLOGY 2008-03-20 — — US disclosed
US-20080057041-A1 Derivation of embryonic stem cells and embryo-derived cells ADVANCED CELL TECHNOLOGY, INC. 2008-03-06 — — US disclosed
WO-2007130664-A2 DERIVATION OF EMBRYONIC STEM CELLS AND EMBRYO-DERIVED CELLS ADVANCED CELL TECHNOLOGY, INC. (US) 2007-11-15 — — WO disclosed
WO-2007062198-A1 METHODS TO ACCELERATE THE ISOLATION OF NOVEL CELL STRAINS FROM PLURIPOTENT STEM CELLS AND CELLS OBTAINED THEREBY ADVANCED CELL TECHNOLOGY, INC. (US) 2007-05-31 — — WO disclosed
US-5847155-A Aromatic pyrrolidine amide prolyl endopeptidase inhibitors PFIZER INC (US) 1998-12-08 — — US disclosed
US-5451571-A Administering Z-proprolinal THE CLEVELAND CLINIC FOUNDATION (US) 1995-09-19 — — US disclosed
EP-0536163-A1 AROMATIC PYRROLIDINE AND THIAZOLIDINE AMIDES PFIZER INC. (US) 1993-04-14 — — EP disclosed
WO-1991018891-A1 AROMATIC PYRROLIDINE AND THIAZOLIDINE AMIDES PFIZER INC. (US) 1991-12-12 — — 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-20230218577-A1 USE OF HEAT SHOCK PROTEIN INHIBITORS FOR THE TREATMENT OF NEURODEVELOPMENTAL DISORDERS HSP90AB1, HSP90AA1, HSF1 DPP4 4568/4885DPP8 4264/4885DPP9 4208/4885

“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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