SCHEMBL2932079

SCHEMBL2932079

O=C(O)CCCCCCCCCCCCCCC(=O)OCc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 1/20 0.59
ALDH1A1 P00352 4/20 0.59
MAPK1 P28482 3/20 0.59
L3MBTL1 Q9Y468 2/20 0.59
MAPT P10636 1/20 0.59
RXFP1 Q9HBX9 1/20 0.59
HDAC3 O15379 2/20 0.53
HDAC4 P56524 2/20 0.53
SLC6A3 Q01959 2/20 0.53
HDAC1 Q13547 2/20 0.53
HDAC7 Q8WUI4 2/20 0.53
HDAC2 Q92769 2/20 0.53
HDAC10 Q969S8 2/20 0.53
HDAC11 Q96DB2 2/20 0.53
HDAC8 Q9BY41 2/20 0.53
HDAC6 Q9UBN7 2/20 0.53
HDAC9 Q9UKV0 2/20 0.53
HDAC5 Q9UQL6 2/20 0.53
ADRA1A P35348 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53

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
SCHEMBL28460828 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL8488876 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL905777 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL16197784 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL17004058 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL8854045 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL9814068 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL8491249 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
SCHEMBL3335775 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT
Sebacic Acid SCHEMBL28606878 1.00 HTT (0.59) HTTALDH1A1MAPK1L3MBTL1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115650852-B Preparation method of octadecanedioic acid mono-tert-butyl ester 天津卡普希科技有限公司 2023-03-17 CN claimed
CN-115650852-A Preparation method of octadecanedioic acid mono-tert-butyl ester 天津卡普希科技有限公司 2023-01-31 CN claimed
US-12178842-B2 PCSK9 antagonist compounds MERCK SHARP & DOHME LLC (US) 2024-12-31 US disclosed
US-11820805-B2 Conjugate based systems for controlled insulin delivery MERCK SHARP & DOHME LLC (US) 2023-11-21 US disclosed
US-20230310551-A1 INSULIN RECEPTOR PARTIAL AGONISTS MERCK SHARP & DOHME LLC (US) 2023-10-05 US disclosed
WO-2023175536-A1 LIPID MONOMERS FOR THERAPEUTIC DELIVERY OF RNA JANSSEN BIOTECH, INC. (US) 2023-09-21 WO disclosed
EP-4204441-A1 INSULIN RECEPTOR PARTIAL AGONISTS Merck Sharp & Dohme LLC (US) 2023-07-05 EP disclosed
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-06-01 US disclosed
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-06-01 US disclosed
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS MERCK SHARP & DOHME LLC 2023-06-01 US disclosed
CN-110656134-B Preparation method of monoester 广东东阳光药业有限公司 2023-03-28 CN disclosed
WO-2007074133-A2 COMPOSITIONS COMPRISING AN ACYLATED INSULIN AND ZINC AND METHOD OF MAKING THE SAID COMPOSITIONS NOVO NORDISK A/S (DK) 2007-07-05 WO disclosed
US-6897326-B2 Asymmetrical bicipital lipid and tubular aggregate formed by using the same JAPAN SCIENCE AND TECHNOLOGY CORPORATION (JP) 2005-05-24 US disclosed
US-20040120998-A1 Novel asymmetrical bicipital lipid and tubular aggregate formed by using the same JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2004-06-24 US disclosed
EP-1396496-A1 NOVEL ASYMMETRICALLY BICIPITAL LIPID AND TUBULAR AGGREGATE FORMED BY USING THE SAME Japan Science and Technology Agency (JP) 2004-03-10 EP disclosed
US-RE36359-E SUCH AS N-(15-CARBOXYPENTADECANOYLOXY)SUCCINIMIDE; USED TO MODIFY PROTEINS TO OBTAIN PROTEIN DERIVATIVES HAVING IMPROVED BIOAVAILABILITY, NO ANTIGENICITY AND CAN BE ADMINISTERED TO ANIMALS KURARAY CO., LTD. (JP) 1999-10-26 US disclosed
EP-0511600-B1 Long chain carboxylic acid imide ester KURARAY CO (JP) 1999-03-17 EP disclosed
US-5414089-A Useful for modifying enzymes or proteins KURARAY CO., LTD. (JP) 1995-05-09 US disclosed
US-5336782-A N-(carboxyalkoyloxy)succinimides; modifiers of proteins and enzymes to prolong their plasma half-lives; nontoxic; antitumor and -carcinogenic agents KURARAY CO., LTD. (JP) 1994-08-09 US disclosed
EP-0511600-A2 Long chain carboxylic acid imide ester KURARAY CO., LTD. (JP) 1992-11-04 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 (4 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-11820805-B2 Conjugate based systems for controlled insulin delivery GPR119, INSR, IGF1R HTT 1774/4885ALDH1A1 1357/4885MAPK1 4342/4885
US-20230165932-A1 PCSK9 ANTAGONIST COMPOUNDS PCSK9, PCSK7, PCSK6 HTT 2214/4885ALDH1A1 4187/4885MAPK1 350/4885
US-12178842-B2 PCSK9 antagonist compounds PCSK9, PCSK7, PCSK6 HTT 2214/4885ALDH1A1 4187/4885MAPK1 350/4885
US-20230310551-A1 INSULIN RECEPTOR PARTIAL AGONISTS INSR, GPR119, IRS1 HTT 2068/4885ALDH1A1 4716/4885MAPK1 3170/4885

“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.