SCHEMBL288962

SCHEMBL288962

N=C(N)NCCC[C@H](NC(=O)[C@@H](N)CCCCN)C(=O)O

nearest known ligand 0.48

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ NPY4R P50391 9/20 0.48
▸ NPY1R P25929 5/20 0.48
▸ NPY2R P49146 4/20 0.48
▸ NPY5R Q15761 4/20 0.48
▸ GNAI3 P08754 1/20 0.47
▸ GNAO1 P09471 1/20 0.47
▸ GNAI1 P63096 1/20 0.47
▸ FOLH1 Q04609 1/20 0.46
▸ GSR P00390 1/20 0.45
▸ NOD1 Q9Y239 1/20 0.43
▸ NRP1 O14786 2/20 0.42
▸ CPB2 Q96IY4 1/20 0.42
▸ DPP8 Q6V1X1 1/20 0.41
▸ DPP9 Q86TI2 1/20 0.41
▸ DPP7 Q9UHL4 1/20 0.41

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
SCHEMBL6806494 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL30016402 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL32932019 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL30017192 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL1067832 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL30528148 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL288961 1.00 NPY4R (0.48) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL15263299 0.97 NPY4R (0.51) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL31694501 0.97 NPY4R (0.51) NPY4RNPY1RNPY2RNPY5RGNAI3
SCHEMBL15263305 0.97 NPY4R (0.51) NPY4RNPY1RNPY2RNPY5RGNAI3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115521359-A Polypeptide nanoparticle composition 深圳厚存纳米药业有限公司 2022-12-27 — — CN claimed
CN-109196004-B Engineered scaffold for vascularized tissue repair 加利福尼亚大学董事会 2022-03-18 — — CN claimed
US-20040067890-A1 Ascorbic acid salts of organic bases with enhanced bioavailability for synergictic anti-aging and skin protective cosmetic compositions GUPTA SHYAM K (US) 2004-04-08 — — US claimed
US-5811401-A Advanced glycosylation endproducts and methods of use therefor THE PICOWER INSTITUTE FOR MEDICAL RESEARCH (US) 1998-09-22 — — US claimed
CN-119709844-B Application of rice gene OsbHLH176,176 in regulation and control of cold resistance 南京农业大学 2026-05-15 — — CN disclosed
US-20250367115-A1 Excipients To Reduce the Viscosity of Antibody Formulations and Formulation Compositions AMGEN INC. (US) 2025-12-04 — — US disclosed
CN-115873803-B Method for improving NK cell survival and anti-tumor activity and application thereof 上海恩凯细胞技术有限公司 2025-06-17 — — CN disclosed
CN-120005928-A Dynamic regulation and control system, strain, construction method of strain and application of strain in microbial fuel cell 天津科技大学 2025-05-16 — — CN disclosed
CN-119709844-A Application of rice gene OsbHLH176,176 in regulation and control of cold resistance 南京农业大学 2025-03-28 — — CN disclosed
US-12257343-B2 Excipients to reduce the viscosity of antibody formulations and formulation compositions AMGEN INC. (US) 2025-03-25 — — US disclosed
CN-117210441-B Low-temperature salt-tolerant beta-glucosidase and application thereof in conversion of ginsenoside Rb1 云南师范大学 2024-09-20 — — CN disclosed
CN-118401257-A Methods for producing antibody peptide conjugates 美国安进公司 2024-07-26 — — CN disclosed
US-20050085540-A1 Vasodilation; anticoagulants; thrombosis; antiproliferative agents ; angiogenesis inhibitors; drug delivery; bioavailability; oral administering UNITED THERAPEUTICS CORPORATION 2005-04-21 — — US disclosed
WO-2005007081-A2 COMPOUNDS AND METHODS FOR DELIVERY OF PROSTACYCLIN ANALOGS UNITED THERAPEUTICS CORPORATION (US) 2005-01-27 — — WO disclosed
US-20040067890-A1 Ascorbic acid salts of organic bases with enhanced bioavailability for synergictic anti-aging and skin protective cosmetic compositions GUPTA SHYAM K (US) 2004-04-08 — — US disclosed
EP-0346460-B1 PURINE DERIVATIVES HAVING PHARMACOLOGICAL ACTION CO PHARMA CORPORATION (IT) 1993-03-10 — — EP disclosed
US-5110798-A Immunomodulators for bone marrow transplants CO PHARMA CORPORATION S.R.L. (IT) 1992-05-05 — — US disclosed
EP-0346460-A1 PURINE DERIVATIVES HAVING PHARMACOLOGICAL ACTION. CO PHARMA CORP SRL (IT) 1989-12-20 — — EP disclosed
WO-1989005818-A1 PURINE DERIVATIVES HAVING PHARMACOLOGICAL ACTION CO PHARMA CORPORATION S.R.L. (IT) 1989-06-29 — — WO disclosed
US-4457907-A Composition and method for protecting a therapeutic drug CLEAR LAKE DEVELOPMENT GROUP (US) 1984-07-03 — — 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 (3 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-20250367115-A1 Excipients To Reduce the Viscosity of Antibody Formulations and Formulation Compositions ARGLU1, ARG1, FCGRT NPY4R 1403/4885NPY1R 1084/4885NPY2R 1670/4885
US-20050085540-A1 Vasodilation; anticoagulants; thrombosis; antiproliferative agents ; angiogenesis inhibitors; drug delivery; bioavailability; oral administering PTGIS, PGF, PLAT NPY4R 1671/4885NPY1R 902/4885NPY2R 1374/4885
US-12257343-B2 Excipients to reduce the viscosity of antibody formulations and formulation compositions ARGLU1, ARG1, FCGRT NPY4R 1403/4885NPY1R 1084/4885NPY2R 1670/4885

“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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