Levacetylleucine

Levacetylleucine

SCHEMBL302605

CC(=O)N[C@@H](CC(C)C)C(=O)O.CCOc1cc([C@H](N)CS(C)(=O)=O)ccc1OC

nearest known ligand 0.45

Full drug profile on Sugi Atlas →

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.45
PDE4B Q07343 15/20 0.45
PDE4C Q08493 12/20 0.45
PDE4A P27815 9/20 0.45
PDE4D Q08499 9/20 0.45
HTR2B P41595 1/20 0.45
FOLH1 Q04609 2/20 0.45
ATM Q13315 1/20 0.44
ALDH1A1 P00352 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
Levacetylleucine SCHEMBL7084218 1.00 LMNA (0.45) LMNAPDE4BPDE4CPDE4APDE4D
Acetylleucine SCHEMBL20474775 1.00 LMNA (0.45) LMNAPDE4BPDE4CPDE4APDE4D
Levacetylleucine SCHEMBL756572 1.00 LMNA (0.45) LMNAPDE4BPDE4CPDE4APDE4D
Levacetylleucine SCHEMBL21229236 1.00 LMNA (0.45) LMNAPDE4BPDE4CPDE4APDE4D
Levacetylleucine SCHEMBL702915 0.94 PDE4B (0.43) LMNAPDE4BPDE4CPDE4APDE4D
Levacetylleucine SCHEMBL703860 0.89 FOLH1 (0.42) LMNAPDE4BPDE4CPDE4APDE4D
Leucine SCHEMBL18074074 0.87 PDE4B (0.48) PDE4BPDE4CPDE4APDE4DHTR2B
Leucine SCHEMBL18074075 0.87 PDE4B (0.48) PDE4BPDE4CPDE4APDE4DHTR2B
SCHEMBL2670612 0.87 LMNA (0.47) LMNAPDE4BPDE4CPDE4APDE4D
SCHEMBL21250512 0.85 FOLH1 (0.45) LMNAPDE4BPDE4CPDE4APDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118851979-A Preparation method of apremilast 潍坊市海欣药业有限公司 2024-10-29 CN claimed
US-11260046-B2 (+)-2-[1-(3-Ethoxy-4- methoxyphenyl)-2-methylsulfonylethyl]- 4-acetylaminoisoindoline-1,3-dione: methods of using and compositions thereof AMGEN INC. (US) 2022-03-01 US claimed
US-10913717-B2 Solid state forms of N-[2-[(I S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methyl sulfonyl)ethyl]-2,3-dihydro-1,3-dioxo-L H-isoindol-4-yl]acetamide and process for preparation thereof MSN LABORATORIES PRIVATE LIMITED (IN) 2021-02-09 US claimed
US-20210023051-A1 (+)-2-[1-(3-ETHOXY-4- METHOXYPHENYL)-2-METHYLSULFONYLETHYL]- 4-ACETYLAMINOISOINDOLINE-1,3-DIONE: METHODS OF USING AND COMPOSITIONS THEREOF AMGEN INC. 2021-01-28 US claimed
US-10781173-B2 Method for preparing apremilast ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD (CN) 2020-09-22 US claimed
US-20200109114-A1 SOLID STATE FORMS OF N-[2-[(I S)-1 -(3-ETHOXY-4-METHOXYPHENYL)-2-(METHYL SULFONYL)ETHYL]-2,3-DIHYDRO-1,3-DIOXO-L H-ISOINDOL-4-YL]ACETAMIDE AND PROCESS FOR PREPARATION THEREOF MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2020-04-09 US claimed
US-20190248740-A1 METHOD FOR PREPARING APREMILAST ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD (CN) 2019-08-15 US claimed
EP-3524242-A1 (+)-2-[1-(3-ETHOXY-4-METHOXYPHENYL)-2-METHYLSULFONYLETHYL]-4-ACETYLAMINOISOINDOLINE-1,3-DIONE: METHODS OF USING AND COMPOSITIONS THEREOF Celgene Corporation (US) 2019-08-14 EP claimed
EP-2420490-B1 Method for the preparation of (+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione CELGENE CORP (US) 2016-07-20 EP claimed
EP-2420490-A1 (+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione: Methods of using and compositions thereof CELGENE CORPORATION (US) 2012-02-22 EP claimed
US-20050192336-A1 Treatment may include administration of a second active agent, including but not limited to, an anti-inflammatory agent, an immnunosuppressant, mycophenolate mofetil, a biologic agent, or a Cox-2 inhibitor AMGEN INC. 2005-09-01 US claimed
US-20030187052-A1 Controrlling concentration of tumor necrosis factor, phosphodiesterase inhibitor; controlling cell differentiation, proliferation; antiinflammatory agents; cardiovascular disorders AMGEN INC. 2003-10-02 US claimed
EP-3619195-B1 NOVEL PROCESS TO PREPARE N-[2-[(1S)-1-(3-ETHOXY-4-METHOXYPHENYL)-2-(METHYLSULPHONYL) ETHYL]-1, 3-DIOXO-2,3-DIHYDRO-1H-ISOINDOL-4-YL]ACETAMIDE UNICHEM LAB LTD (IN) 2025-07-23 EP disclosed
CN-119390623-A Racemization preparation method of apremilast and intermediate thereof 菏泽皓元医药科技有限公司 2025-02-07 CN disclosed
CN-118851979-A Preparation method of apremilast 潍坊市海欣药业有限公司 2024-10-29 CN disclosed
EP-3702347-B1 PROCESSES FOR THE PREPARATION OF (S)-1-(3-ETHOXY-4- METHOXYPHENYL)-2-METHANESULFONYLETHYLAMINE AMGEN EUROPE GMBH (CH) 2023-11-08 EP disclosed
US-20050192336-A1 Treatment may include administration of a second active agent, including but not limited to, an anti-inflammatory agent, an immnunosuppressant, mycophenolate mofetil, a biologic agent, or a Cox-2 inhibitor AMGEN INC. 2005-09-01 US disclosed
EP-1485087-A1 (+)-2- 1-(3-ETHOXY-4-METHOXYPHENYL)-2-METHYLSULFONYLETHYL]-4-ACETYLAMINOISOINDOLINE-1,3-DIONE: METHODS OF USING AND COMPOSITIONS THEREOF CELGENE CORPORATION (US) 2004-12-15 EP disclosed
US-20030187052-A1 Controrlling concentration of tumor necrosis factor, phosphodiesterase inhibitor; controlling cell differentiation, proliferation; antiinflammatory agents; cardiovascular disorders AMGEN INC. 2003-10-02 US disclosed
WO-2003080049-A1 (+)-2-[1-(3-ETHOXY-4-METHOXYPHENYL)-2-METHYLSULFONYLETHYL]-4-ACETYLAMINOISOINDOLINE-1,3-DIONE: METHODS OF USING AND COMPOSITIONS THEREOF CELGENE CORPORATION (US) 2003-10-02 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 (8 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-20030187052-A1 Controrlling concentration of tumor necrosis factor, phosphodiesterase inhibitor; controlling cell differentiation, proliferation; antiinflammatory agents; cardiovascular disorders PDE4A, PDE2A, PDE3A LMNA 1170/4885PDE4B 6/4885PDE4C 8/4885
US-10913717-B2 Solid state forms of N-[2-[(I S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methyl sulfonyl)ethyl]-2,3-dihydro-1,3-dioxo-L H-isoindol-4-yl]acetamide and process for preparation thereof SULT1A1, SULT2A1, SULT1E1 LMNA 1467/4885PDE4B 2424/4885PDE4C 2986/4885
US-20200109114-A1 SOLID STATE FORMS OF N-[2-[(I S)-1 -(3-ETHOXY-4-METHOXYPHENYL)-2-(METHYL SULFONYL)ETHYL]-2,3-DIHYDRO-1,3-DIOXO-L H-ISOINDOL-4-YL]ACETAMIDE AND PROCESS FOR PREPARATION THEREOF SULT1A1, SULT2A1, SULT1E1 LMNA 1467/4885PDE4B 2424/4885PDE4C 2986/4885
US-20050192336-A1 Treatment may include administration of a second active agent, including but not limited to, an anti-inflammatory agent, an immnunosuppressant, mycophenolate mofetil, a biologic agent, or a Cox-2 inhibitor IL4, PTGER4, PDE4A LMNA 3162/4885PDE4B 7/4885PDE4C 11/4885
US-11260046-B2 (+)-2-[1-(3-Ethoxy-4- methoxyphenyl)-2-methylsulfonylethyl]- 4-acetylaminoisoindoline-1,3-dione: methods of using and compositions thereof PDE4A, PDE4B, PDE2A LMNA 1491/4885PDE4B 2/4885PDE4C 7/4885
US-10781173-B2 Method for preparing apremilast CMA1, ACE, AGT LMNA 1064/4885PDE4B 3492/4885PDE4C 3783/4885
US-20190248740-A1 METHOD FOR PREPARING APREMILAST CMA1, ACE, AGT LMNA 1064/4885PDE4B 3492/4885PDE4C 3783/4885
US-20210023051-A1 (+)-2-[1-(3-ETHOXY-4- METHOXYPHENYL)-2-METHYLSULFONYLETHYL]- 4-ACETYLAMINOISOINDOLINE-1,3-DIONE: METHODS OF USING AND COMPOSITIONS THEREOF PDE4A, PDE4B, PDE2A LMNA 1491/4885PDE4B 2/4885PDE4C 7/4885

“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.