SCHEMBL2993356

SCHEMBL2993356

O=C(O)CCCCCC(=O)C(=O)O

nearest known ligand 0.94

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 5/20 0.71
LMNA P02545 3/20 0.71
NFKB1 P19838 1/20 0.71
PMP22 Q01453 1/20 0.71
OR51E2 Q9H255 2/20 0.63
MAPK1 P28482 1/20 0.63
SLC13A3 Q8WWT9 1/20 0.63
EGLN1 Q9GZT9 1/20 0.63
GPR84 Q9NQS5 8/20 0.57
FFAR1 O14842 2/20 0.57
FFAR4 Q5NUL3 2/20 0.57
SLC22A6 Q4U2R8 2/20 0.56
PPARG P37231 6/20 0.55
PPARD Q03181 6/20 0.55
PPARA Q07869 6/20 0.55
HDAC11 Q96DB2 5/20 0.55
ALDH1A1 P00352 3/20 0.55
TLR2 O60603 2/20 0.55
TDP1 Q9NUW8 2/20 0.55
MEN1 O00255 2/20 0.55

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
SCHEMBL2780784 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL9186388 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL20537125 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL2780957 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL9794734 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL4389370 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL10592204 1.00 TSHR (0.71) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL15054423 0.97 TSHR (0.67) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL14357994 0.97 LMNA (0.69) TSHRLMNANFKB1PMP22OR51E2
SCHEMBL259198 0.97 LMNA (0.69) TSHRLMNANFKB1PMP22OR51E2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230022727-A1 MICROORGANISMS AND METHODS FOR THE BIOSYNTHESIS OF ADIPATE, HEXAMETHYLENEDIAMINE AND 6-AMINOCAPROIC ACID GENOMATICA INC (US) 2023-01-26 US claimed
US-9580731-B2 Methods of producing 7-carbon chemicals via c1 carbon chain elongation associated with coenzyme B synthesis INVISTA NORTH AMERICA S.A.R.L. (US) 2017-02-28 US claimed
CN-105189764-A Methods of producing 7-carbon chemicals via C1 carbon chain elongation associated with coenzyme B synthesis INVISTA TECH SARL 2015-12-23 CN claimed
EP-2938736-A2 METHODS OF PRODUCING 7-CARBON CHEMICALS VIA C1 CARBON CHAIN ELONGATION ASSOCIATED WITH COENZYME B SYNTHESIS Invista Technologies S.A R.L. (CH) 2015-11-04 EP claimed
US-20140193863-A1 Methods Of Producing 7-Carbon Chemicals Via C1 Carbon Chain Elongation Associated With Coenzyme B Synthesis INVISTA North America S.á r.I. (US) 2014-07-10 US claimed
WO-2014105790-A2 METHODS OF PRODUCING 7-CARBON CHEMICALS VIA C1 CARBON CHAIN ELONGATION ASSOCIATED WITH COENZYME B SYNTHESIS INVISTA NORTH AMERICA S.A.R.L. (US) 2014-07-03 WO claimed
WO-2026101867-A1 PROCESS FOR PREPARING A MACROCYCLIC DIAMINE, INTERMEDIATES, AND CRYSTALLINE FORMS THEREOF MERCK SHARP & DOHME LLC (US) 2026-05-15 WO disclosed
US-12577591-B2 Microorganisms and methods for increasing co-factors GENOMATICA, INC. (US) 2026-03-17 US disclosed
US-20260028651-A1 METHOD OF PRODUCING & PROCESSING DIAMINES AGAIN BIO APS (DK) 2026-01-29 US disclosed
US-12503711-B2 Method of producing and processing diamines to a diamine free base using a carbonate intermediate and an engineered microorganism GENOMATICA, INC. (US) 2025-12-23 US disclosed
CN-116023365-B Ketohexokinase inhibitors and uses thereof 轩竹生物科技股份有限公司 2025-02-14 CN disclosed
CN-114728871-B Microorganisms and methods for reducing byproducts 基因组股份公司 2024-12-27 CN disclosed
US-20240141397-A1 MICROORGANISMS AND METHODS FOR THE PRODUCTION OF BIOSYNTHESIZED TARGET PRODUCTS HAVING REDUCED LEVELS OF BYPRODUCTS AGAIN BIO APS (DK) 2024-05-02 US disclosed
US-20120028320-A1 PREPARATION OF ADIPIC ACID DSM IP ASSETS B.V. (NL) 2012-02-02 US disclosed
CN-102317464-A From alpha-ketoacid biosynthesizing difunctionality alkane CELEXION LLC 2012-01-11 CN disclosed
CN-102307872-A BCL-2-selectively apoptosis-inducing agents for the treatment of cancer and immune diseases ABBOTT LAB 2012-01-04 CN disclosed
CN-101910142-A The conditioning agent of amyloid beta HOFFMANN LA ROCHE 2010-12-08 CN disclosed
US-7780801-B2 for soldering flip chip surfaces; fluxing agent comprises keto acid such as levulinic acid or acetylbutyric acid; mixture of tacky solvent (ethoxylated glycerol) with non-tacky solvent (methanol) INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2010-08-24 US disclosed
US-20100175790-A1 New Flux Composition and Process For Use Thereof INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2010-07-15 US disclosed
US-20080124568-A1 New flux composition and process for use thereof GLOBALFOUNDRIES INC. (KY) 2008-05-29 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 (2 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-20260028651-A1 METHOD OF PRODUCING & PROCESSING DIAMINES DDC, DAO, ODC1 TSHR 3382/4885LMNA 2536/4885NFKB1 2164/4885
US-12577591-B2 Microorganisms and methods for increasing co-factors ABAT, HADHB, MMAB TSHR 4263/4885LMNA 1752/4885NFKB1 1282/4885

“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.