SCHEMBL10310207

SCHEMBL10310207

CC(C)(C)OC(=O)N[C@@H](Cc1cn(C(=O)OC(C)(C)C)c2ccccc12)C(=O)O

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ ADAM17 P78536 1/20 0.58
▸ L3MBTL1 Q9Y468 1/20 0.55
▸ CTSS P25774 3/20 0.50
▸ CTSK P43235 3/20 0.50
▸ ACE P12821 2/20 0.49
▸ CCKAR P32238 3/20 0.49
▸ CCKBR P32239 3/20 0.49
▸ OPRD1 P41143 3/20 0.49
▸ EPHX1 P07099 1/20 0.48
▸ SCN9A Q15858 1/20 0.47
▸ MAPK1 P28482 1/20 0.46
▸ CTSL P07711 2/20 0.46
▸ PPARA Q07869 2/20 0.45
▸ PPARG P37231 1/20 0.45
▸ PDE10A Q9Y233 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
SCHEMBL29401320 1.00 ADAM17 (0.58) ADAM17L3MBTL1CTSSCTSKACE
SCHEMBL4294679 1.00 ADAM17 (0.58) ADAM17L3MBTL1CTSSCTSKACE
SCHEMBL22804050 1.00 ADAM17 (0.58) ADAM17L3MBTL1CTSSCTSKACE
SCHEMBL29400491 1.00 ADAM17 (0.58) ADAM17L3MBTL1CTSSCTSKACE
SCHEMBL29401255 0.91 ADAM17 (0.58) ADAM17L3MBTL1CTSSCTSKCCKAR
SCHEMBL18002447 0.91 CTSS (0.50) ADAM17L3MBTL1CTSSCTSKACE
SCHEMBL29401597 0.91 ADAM17 (0.58) ADAM17L3MBTL1CTSSCTSKCCKAR
SCHEMBL21309886 0.90 L3MBTL1 (0.57) ADAM17L3MBTL1CTSSCTSKCCKAR
SCHEMBL29169598 0.90 L3MBTL1 (0.57) ADAM17L3MBTL1CTSSCTSKCCKAR
SCHEMBL22804106 0.90 ADAM17 (0.53) ADAM17L3MBTL1ACECCKARCCKBR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3988538-A1 MODIFIED HYDROPHOBIC AUXILIARY MATERIAL, PREPARATION METHOD THEREFOR AND USE THEREOF Zhejiang Zhida Pharmaceutical Co., Ltd. (CN) 2022-04-27 — — EP claimed
US-20220111055-A1 MODIFIED HYDROPHOBIC EXCIPIENT AND PREPARATION METHOD THEREOF ZHEJIANG ZHIDA PHARMACEUTICAL CO., LTD. (CN) 2022-04-14 — — US claimed
CN-112480122-B Tetrahydroimidazo [1,2-a ] pyrazine compound, composition, preparation method and application thereof 中山大学 2022-03-22 — — CN claimed
WO-2020252713-A1 MODIFIED HYDROPHOBIC AUXILIARY MATERIAL, PREPARATION METHOD THEREFOR AND USE THEREOF 浙江智达药业有限公司 2020-12-24 — — WO claimed
US-12616676-B2 Preparation method and use of modified hydrophobic excipient ZHEJIANG ZHIDA PHARMACEUTICAL CO., LTD. (CN) 2026-05-05 — — US disclosed
EP-3988538-B1 MODIFIED HYDROPHOBIC AUXILIARY MATERIAL, PREPARATION METHOD THEREFOR AND USE THEREOF ZHEJIANG ZHIDA PHARMACEUTICAL CO LTD (CN) 2024-08-07 — — EP disclosed
EP-3988538-A1 MODIFIED HYDROPHOBIC AUXILIARY MATERIAL, PREPARATION METHOD THEREFOR AND USE THEREOF Zhejiang Zhida Pharmaceutical Co., Ltd. (CN) 2022-04-27 — — EP disclosed
US-20220111055-A1 MODIFIED HYDROPHOBIC EXCIPIENT AND PREPARATION METHOD THEREOF ZHEJIANG ZHIDA PHARMACEUTICAL CO., LTD. (CN) 2022-04-14 — — US disclosed
US-20220111056-A1 DRUG-LOADED EMULSION ZHEJIANG ZHIDA PHARMACEUTICAL CO., LTD. (CN) 2022-04-14 — — US disclosed
US-20220110909-A1 PREPARATION METHOD AND USE OF MODIFIED HYDROPHOBIC EXCIPIENT ZHEJIANG ZHIDA PHARMACEUTICAL CO., LTD. (CN) 2022-04-14 — — US disclosed
CN-112480122-B Tetrahydroimidazo [1,2-a ] pyrazine compound, composition, preparation method and application thereof 中山大学 2022-03-22 — — CN disclosed
CN-112480122-A Tetrahydroimidazo [1,2-a ] pyrazine compound, composition, preparation method and application thereof 中山大学 2021-03-12 — — CN disclosed
US-8513187-B2 Soft protease inhibitors, and pro-soft forms thereof TRUSTEES OF TUFTS COLLEGE (US) 2013-08-20 — — US disclosed
US-20120178677-A1 SOFT PROTEASE INHIBITORS, AND PRO-SOFT FORMS THEREOF TRUSTEES OF TUFTS COLLEGE (US) 2012-07-12 — — US disclosed
US-7893042-B2 Boc-glycyl-phenazopyridine; phenazopyridines covalently attached to various conjugates; useful for providing increased (oral) bioavailability with reduced side effects PINNACLE PHARMACEUTICALS, INC. (US) 2011-02-22 — — US disclosed
US-20100204185-A1 PHENAZOPYRIDINE COMPOUNDS PINNACLE PHARMACEUTICALS, INC. (US) 2010-08-12 — — 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-12616676-B2 Preparation method and use of modified hydrophobic excipient CETP, LIPA, MTTP ADAM17 2068/4885L3MBTL1 3657/4885CTSS 2330/4885
US-20100204185-A1 PHENAZOPYRIDINE COMPOUNDS CYP3A5, CYP3A4, CYP2D6 ADAM17 4275/4885L3MBTL1 4799/4885CTSS 2668/4885
US-20120178677-A1 SOFT PROTEASE INHIBITORS, AND PRO-SOFT FORMS THEREOF DPP4, LIPE, PREP ADAM17 41/4885L3MBTL1 556/4885CTSS 111/4885
US-20220111056-A1 DRUG-LOADED EMULSION SLC43A1, SLC7A1, CETP ADAM17 3404/4885L3MBTL1 799/4885CTSS 3871/4885
US-20220111055-A1 MODIFIED HYDROPHOBIC EXCIPIENT AND PREPARATION METHOD THEREOF CETP, SLC43A1, SLC27A1 ADAM17 2880/4885L3MBTL1 554/4885CTSS 3839/4885
US-20220110909-A1 PREPARATION METHOD AND USE OF MODIFIED HYDROPHOBIC EXCIPIENT ABCG2, CYP51A1, HACD3 ADAM17 1796/4885L3MBTL1 3778/4885CTSS 1383/4885

“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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