SCHEMBL7423487

SCHEMBL7423487

CCSSC[C@H](NC(=O)OC(C)(C)C)C(=O)O

nearest known ligand 0.55

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PPARA Q07869 11/20 0.55
PPARG P37231 10/20 0.55
PPARD Q03181 2/20 0.53
CYP1A2 P05177 1/20 0.51
CYP2C9 P11712 1/20 0.51
CYP2C19 P33261 1/20 0.51
HTT P42858 1/20 0.51
CTSK P43235 6/20 0.48
CTSS P25774 5/20 0.48
SMN1; SMN2 Q16637 1/20 0.47
ITGB3 P05106 1/20 0.43
ITGA2B P08514 1/20 0.43
CTSL P07711 1/20 0.43
CTSB P07858 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
SCHEMBL16289560 1.00 PPARA (0.55) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL5351802 0.94 PPARA (0.57) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL316084 0.94 PPARA (0.57) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL13489723 0.94 PPARA (0.57) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL432222 0.94 PPARA (0.57) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL2541324 0.94 PPARA (0.57) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL10692756 0.88 PPARA (0.50) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL22636121 0.88 CYP1A2 (0.55) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL22636123 0.88 CYP1A2 (0.55) PPARAPPARGPPARDCYP1A2CYP2C9
SCHEMBL22381014 0.88 PPARA (0.55) PPARAPPARGPPARDCYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240166689-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-05-23 US disclosed
US-11891457-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-06 US disclosed
EP-2813512-B1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI PHARMACEUTICAL CO LTD (JP) 2021-03-31 EP disclosed
US-20210061860-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2021-03-04 US disclosed
US-20160311858-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-10-27 US disclosed
US-9409952-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-08-09 US disclosed
US-20150080549-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2015-03-19 US disclosed
EP-2813512-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD Chugai Seiyaku Kabushiki Kaisha (JP) 2014-12-17 EP disclosed
US-20100221749-A1 THREE-FUNCTIONAL PSEUDO-PEPTIDIC REAGENT, AND USES AND APPLICATIONS THEREOF UNIVERSITE DE ROUEN 2010-09-02 US disclosed
US-20100221749-A1 THREE-FUNCTIONAL PSEUDO-PEPTIDIC REAGENT, AND USES AND APPLICATIONS THEREOF UNIVERSITE DE ROUEN 2010-09-02 US disclosed
US-4414149-A POLYPEPTIDE ARMOUR PHARMACEUTICAL COMPANY (US) 1983-11-08 US disclosed
US-4401593-A CYCLIC POLYPEPTIDES ARMOUR PHARMACEUTICAL COMPANY (US) 1983-08-30 US disclosed
US-4397780-A SUBSTITUTION ALALOGS OF NATURAL CALCITONINS ARMOUR PHARMACEUTICAL COMPANY (US) 1983-08-09 US disclosed
US-4391747-A CALCITONIN PEPTIDES ARMOUR PHARMACEUTICAL COMPANY (US) 1983-07-05 US disclosed
US-4388235-A SYNTHETIC CALCITONIN ARMOUR PHARMACEUTICAL COMPANY (US) 1983-06-14 US disclosed
US-4304692-A RESIN PEPTIDE FOR MAKING CALCITONIN ANALOGUES ARMOUR PHARMACEUTICAL COMPANY (US) 1981-12-08 US disclosed
US-4239680-A CALCITONIN ACITIVITY ARMOUR AND COMPANY (US) 1980-12-16 US disclosed
US-4217268-A CALCITONINS RHONE-POULENC RORER PHARMACEUTICALS INC. 1980-08-12 US disclosed
US-4212795-A TO FORM DISULFIDE BOND ARMOUR PHARMACEUTICAL COMPANY (US) 1980-07-15 US disclosed
US-4062815-A DIVINYLBENZENE CROSSLINKED POLYSTYRENE ARMOUR PHARMACEUTICAL COMPANY (US) 1977-12-13 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 (6 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-11891457-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R PPARA 3215/4885PPARG 3973/4885PPARD 3438/4885
US-20210061860-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R PPARA 3215/4885PPARG 3973/4885PPARD 3438/4885
US-20240166689-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R PPARA 3215/4885PPARG 3973/4885PPARD 3438/4885
US-20160311858-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R PPARA 3215/4885PPARG 3973/4885PPARD 3438/4885
US-20150080549-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R PPARA 3215/4885PPARG 3973/4885PPARD 3438/4885
US-20100221749-A1 THREE-FUNCTIONAL PSEUDO-PEPTIDIC REAGENT, AND USES AND APPLICATIONS THEREOF DNPEP, PEPD, LNPEP PPARA 4436/4885PPARG 4419/4885PPARD 4413/4885

“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.