SCHEMBL808737

SCHEMBL808737

CCCC(CCC)(C(=O)OC)C(=O)OC

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
DGAT1 O75907 1/20 0.36
ALDH1A1 P00352 4/20 0.35
LMNA P02545 2/20 0.35
HSD17B10 Q99714 1/20 0.35
POLB P06746 1/20 0.34
PTPRB P23467 2/20 0.33
TSHR P16473 1/20 0.33
MAPT P10636 1/20 0.32
ATM Q13315 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.32
ELANE P08246 1/20 0.32
THRB P10828 1/20 0.32
PKM P14618 1/20 0.32
KCNN4 O15554 1/20 0.32
EPHX1 P07099 1/20 0.32
FDPS P14324 2/20 0.32
USP2 O75604 1/20 0.32
HTT P42858 1/20 0.31

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
SCHEMBL18346585 0.92 ALDH1A1 (0.37) MEN1KMT2ADGAT1ALDH1A1LMNA
SCHEMBL29067495 0.91 EPHX1 (0.36) MEN1KMT2AALDH1A1LMNAPOLB
SCHEMBL28655390 0.89 MEN1 (0.32) MEN1KMT2ADGAT1ALDH1A1LMNA
SCHEMBL29082258 0.89 MEN1 (0.53) MEN1KMT2AALDH1A1LMNAHSD17B10
SCHEMBL9723233 0.88 ALDH1A1 (0.33) MEN1KMT2ADGAT1ALDH1A1LMNA
SCHEMBL28871790 0.88 PTPN1 (0.37) MEN1KMT2ADGAT1ALDH1A1LMNA
SCHEMBL27908938 0.87 MEN1 (0.39) MEN1KMT2AALDH1A1LMNAHSD17B10
SCHEMBL15233853 0.85 EPHX1 (0.39) MEN1KMT2ADGAT1ALDH1A1LMNA
SCHEMBL25200704 0.83 MEN1 (0.44) MEN1KMT2ALMNAMAPTATM
SCHEMBL28167346 0.83 MMP8 (0.40) LMNATSHRUSP2CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118373737-A Preparation, hydrolysis and application of dipropyldimethyl malonate 湖南大学 2024-07-23 CN claimed
US-5344975-A Process for production of lower alkanoic acids WYCKOFF CHEMICAL COMPANY, INC. (US) 1994-09-06 US claimed
US-12637680-B2 Recombinant host cells for the production of malonate LYGOS, INC. (US) 2026-05-26 US disclosed
CN-119709450-A Recombinant host cells for malonate production 利戈斯股份有限公司 2025-03-28 CN disclosed
CN-119462378-A Recovery and comprehensive utilization of dipropylmalonic monoester 湖南大学 2025-02-18 CN disclosed
CN-114616330-B Recombinant host cells for malonate production 利戈斯股份有限公司 2025-01-03 CN disclosed
CN-118373737-A Preparation, hydrolysis and application of dipropyldimethyl malonate 湖南大学 2024-07-23 CN disclosed
US-20240191216-A1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE LYGOS, INC. (US) 2024-06-13 US disclosed
CN-116768697-B Method for preparing dipropylmalonic acid by using chloropropane as alkylating agent and application of dipropylmalonic acid 湖南大学 2024-03-29 CN disclosed
WO-2024054828-A2 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE LYGOS, INC. (US) 2024-03-14 WO disclosed
CN-116023232-B Preparation method of propyl malonic acid and homologs thereof 湖南省湘中制药有限公司 2024-03-08 CN disclosed
US-20080076941-A1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUNDS, PROCESS FOR PRODUCTION OF THE SAME AND USE THEREOF ITAGAKI MAKOTO 2008-03-27 US disclosed
US-20080076931-A1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUNDS, PROCESS FOR PRODUCTION OF THE SAME AND USE THEREOF ITAGAKI MAKOTO 2008-03-27 US disclosed
US-7288674-B2 Optically active bisoxazoline compounds, process for production of the same and use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-10-30 US disclosed
US-20060149077-A1 Optically active bisoxazoline compounds, process for production of the same and use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-07-06 US disclosed
EP-1593674-A1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUNDS, PROCESS FOR PRODUCTION OF THE SAME AND USE THEREOF Sumitomo Chemical Company, Limited (JP) 2005-11-09 EP disclosed
US-5344975-A Process for production of lower alkanoic acids WYCKOFF CHEMICAL COMPANY, INC. (US) 1994-09-06 US disclosed
EP-0055797-B1 PROCESS FOR THE PREPARATION OF SUBSTITUTED ACETIC ACIDS AND/OR OF THEIR ESTERS AND OF SUBSTITUTED ACETONITRILES, RESPECTIVELY HÜLS TROISDORF AKTIENGESELLSCHAFT (DE) 1985-05-29 EP disclosed
US-4417073-A Process for the preparation of substituted acetic acids and derivatives thereof DYNAMIT NOBEL A.G. (DE) 1983-11-22 US disclosed
EP-0055797-A1 Process for the preparation of substituted acetic acids and/or of their esters and of substituted acetonitriles, respectively HÜLS TROISDORF AKTIENGESELLSCHAFT (DE) 1982-07-14 EP 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 (5 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-20060149077-A1 Optically active bisoxazoline compounds, process for production of the same and use thereof ACSL3, ADSL, SQLE MEN1 3119/4885KMT2A 4666/4885DGAT1 2839/4885
US-20080076941-A1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUNDS, PROCESS FOR PRODUCTION OF THE SAME AND USE THEREOF ACSL3, ADSL, SQLE MEN1 3119/4885KMT2A 4666/4885DGAT1 2839/4885
US-20080076931-A1 OPTICALLY ACTIVE BISOXAZOLINE COMPOUNDS, PROCESS FOR PRODUCTION OF THE SAME AND USE THEREOF ACSL3, ADSL, SQLE MEN1 3119/4885KMT2A 4666/4885DGAT1 2839/4885
US-12637680-B2 Recombinant host cells for the production of malonate DCXR, ETV1, LYPLA2 MEN1 4165/4885KMT2A 361/4885DGAT1 387/4885
US-20240191216-A1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE ME1, MAL2, ME3 MEN1 1464/4885KMT2A 4341/4885DGAT1 1582/4885

“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.