SCHEMBL3473844

SCHEMBL3473844

CC(O)CC(=O)OP(=O)(O)O

nearest known ligand 0.42

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CA4 P22748 1/20 0.37
PGK1 P00558 1/20 0.34
PGK2 P07205 1/20 0.34
PEPD P12955 1/20 0.33
PGD P52209 2/20 0.32
LPAR6 P43657 1/20 0.31
LPAR1 Q92633 1/20 0.31
LPAR4 Q99677 1/20 0.31
LPAR5 Q9H1C0 1/20 0.31
LPAR2 Q9HBW0 1/20 0.31
LPAR3 Q9UBY5 1/20 0.31
ENPP2 Q13822 1/20 0.31
LAP3 P28838 2/20 0.31
ALDH1A1 P00352 1/20 0.30
MMP1 P03956 1/20 0.30
MMP8 P22894 1/20 0.30

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
SCHEMBL19329928 1.00 CA4 (0.37) CA4PGK1PGK2PEPDPGD
SCHEMBL3473841 1.00 CA4 (0.37) CA4PGK1PGK2PEPDPGD
SCHEMBL3473839 0.84 MAPT (0.31)
SCHEMBL17606430 0.84 MMP1 (0.42) CA4PEPDLAP3ALDH1A1MMP1
SCHEMBL16094426 0.84 MAPT (0.31)
SCHEMBL16093956 0.84 BTN3A1 (0.35) PGK1PGK2LPAR1LPAR3
SCHEMBL17423808 0.81 CA4 (0.40) CA4PGK1PGK2PEPDPGD
SCHEMBL17281367 0.80 CA4 (0.41) CA4LAP3ALDH1A1
SCHEMBL16093955 0.80
SCHEMBL5789749 0.79 CA4 (0.37) CA4PGK1PGK2PGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220220511-A1 MICROORGANISMS AND METHODS FOR PRODUCING BUTADIENE AND RELATED COMPOUNDS BY FORMATE ASSIMILATION GENOMATICA INC (US) 2022-07-14 US claimed
US-12529078-B2 Microorganisms and methods for improving product yields on methanol using acetyl-CoA synthesis GENOMATICA, INC. (US) 2026-01-20 US disclosed
US-20240294950-A1 MICROORGANISMS AND METHODS FOR IMPROVING PRODUCT YIELDS ON METHANOL USING ACETYL-COA SYNTHESIS AGAIN BIO APS (DK) 2024-09-05 US disclosed
EP-4421181-A2 NON-NATURAL MICROBIAL ORGANISMS WITH IMPROVED ENERGETIC EFFICIENCY Genomatica, Inc. (US) 2024-08-28 EP disclosed
EP-3741865-B1 NON-NATURAL MICROBIAL ORGANISMS WITH IMPROVED ENERGETIC EFFICIENCY GENOMATICA INC (US) 2024-03-13 EP disclosed
EP-4296364-A2 MICROORGANISMS AND METHODS FOR IMPROVING PRODUCT YIELDS ON METHANOL USING ACETYL-COA SYNTHESIS Genomatica, Inc. (US) 2023-12-27 EP disclosed
EP-3967747-B1 MICROORGANISMS AND METHODS FOR IMPROVING PRODUCT YIELDS ON METHANOL USING ACETYL-COA SYNTHESIS GENOMATICA INC (US) 2023-11-08 EP disclosed
US-20230126921-A1 NON-NATURAL MICROBIAL ORGANISMS WITH IMPROVED ENERGETIC EFFICIENCY AGAIN BIO APS (DK) 2023-04-27 US disclosed
CN-110049760-B Composition for treating inflammatory diseases, application thereof and probiotic composition 链生物技术有限公司 2022-09-16 CN disclosed
US-20220220511-A1 MICROORGANISMS AND METHODS FOR PRODUCING BUTADIENE AND RELATED COMPOUNDS BY FORMATE ASSIMILATION GENOMATICA INC (US) 2022-07-14 US disclosed
WO-2015084633-A1 MICROORGANISMS AND METHODS FOR IMPROVING PRODUCT YIELDS ON METHANOL USING ACETYL-COA SYNTHESIS GENOMATICA, INC. (US) 2015-06-11 WO disclosed
US-20150050708-A1 MICROORGANISMS AND METHODS FOR PRODUCING BUTADIENE AND RELATED COMPOUNDS BY FORMATE ASSIMILATION GENOMATICA, INC. (US) 2015-02-19 US disclosed
WO-2014152434-A2 MICROORGANISMS AND METHODS FOR PRODUCING BUTADIENE AND RELATED COMPOUNDS BY FORMATE ASSIMILATION GENOMATICA, INC. (US) 2014-09-25 WO disclosed
EP-2176415-B1 PREPARING METHOD FOR (S)-3-HYDROXYBUTYRIC ACID AND (S)-3-HYDROXYBUTYRATE ESTER USING RECOMBINANT MICROORGANISM LG CHEMICAL LTD (KR) 2014-05-07 EP disclosed
CN-101802200-B Preparing method for (s)-3-hydroxybutyric acid and (s)-3-hydroxybutyrate ester using recombinant microorganism LG CHEMICAL LTD 2013-11-20 CN disclosed
US-8535918-B2 Preparing method for (S)-3hydroxybutyric acid and (S)-3 hydroxybutyrate ester using recombinant microorganism LG CHEM, LTD. (KR) 2013-09-17 US disclosed
US-20100209983-A1 PREPARING METHOD FOR (S)-3HYDROXYBUTYRIC ACID AND (S)-3 HYDROXYBUTYRATE ESTER USING RECOMBINANT MICROORGANISM LG-CHEM, LTD. (KR) 2010-08-19 US disclosed
CN-101802200-A Preparing method for (s)-3-hydroxybutyric acid and (s)-3-hydroxybutyrate ester using recombinant microorganism LG CHEMICAL LTD 2010-08-11 CN disclosed
EP-2176415-A1 PREPARING METHOD FOR (S)-3-HYDROXYBUTYRIC ACID AND (S)-3-HYDROXYBUTYRATE ESTER USING RECOMBINANT MICROORGANISM LG Chem. Ltd. (KR) 2010-04-21 EP disclosed
WO-2009020279-A1 PREPARING METHOD FOR (S)-3-HYDROXYBUTYRIC ACID AND (S)-3-HYDROXYBUTYRATE ESTER USING RECOMBINANT MICROORGANISM LG CHEM, LTD. (KR) 2009-02-12 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 (1 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-12529078-B2 Microorganisms and methods for improving product yields on methanol using acetyl-CoA synthesis ALDOA, FDPS, DERA CA4 683/4885PGK1 415/4885PGK2 552/4885

“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.