SCHEMBL2992495

SCHEMBL2992495

COC(=O)C(C)P(C)(C)=O

nearest known ligand 0.42

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CA2 P00918 6/20 0.42
CA12 O43570 5/20 0.42
MMP2 P08253 5/20 0.42
CA1 P00915 5/20 0.42
MMP1 P03956 4/20 0.42
CA9 Q16790 4/20 0.42
MMP8 P22894 3/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
MMP9 P14780 1/20 0.42
CA14 Q9ULX7 2/20 0.39
MMP3 P08254 1/20 0.37
KDM4E B2RXH2 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
ALDH1A1 P00352 2/20 0.32
KMT2A Q03164 1/20 0.32
ACHE P22303 1/20 0.32

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
SCHEMBL2452794 0.87 CA12 (0.41) CA2CA12MMP2CA1MMP1
SCHEMBL8132488 0.84 CA12 (0.42) CA2CA12MMP2CA1MMP1
SCHEMBL12011596 0.80 SMN1; SMN2 (0.39) CA2CA12MMP2CA1MMP1
SCHEMBL10366299 0.80 MMP1 (0.39) CA2CA12MMP2CA1MMP1
SCHEMBL2978531 0.77 SMN1; SMN2 (0.41) CA2CA12MMP2CA1MMP1
SCHEMBL2403902 0.77 GABRR1 (0.39) CA2CA12MMP2CA1MMP1
Phosphoric Acid SCHEMBL28708565 0.76 CA12 (0.44) CA2CA12MMP2CA1MMP1
SCHEMBL2978555 0.75 ALDH1A1 (0.42) MMP2MMP1MMP3TDP1ALDH1A1
SCHEMBL12549416 0.75 SMN1; SMN2 (0.44) CA2CA12MMP2CA1MMP1
SCHEMBL11957056 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4066690-A CHEMICAL INTERMEDIATES FOR PROSTAGLANDINS HOECHST AKTIENGESELLSCHAFT (DT) 1978-01-03 US claimed
US-20240217930-A1 SARS-COV-2 MPRO INHIBITOR COMPOUNDS HEPTARES THERAPEUTICS LIMITED (GB) 2024-07-04 US disclosed
US-20240024338-A1 CARBIDOPA AND L-DOPA PRODRUGS AND METHODS OF USE ABBVIE INC (US) 2024-01-25 US disclosed
US-20180208552-A1 UREA DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF KYORIN PHARMACEUTICAL CO., LTD. (JP) 2018-07-26 US disclosed
US-20180079762-A1 Carbidopa and L-Dopa Prodrugs and Methods of use ABBVIE INC. (US) 2018-03-22 US disclosed
US-20170081363-A1 PHARMACEUTICALLY RELEVANT AROMATIC-CATIONIC PEPTIDES STEALTH BIOTHERAPEUTICS CORP (MC) 2017-03-23 US disclosed
US-20160362431-A1 Carbidopa And L-Dopa Prodrugs And Methods Of Use ABBVIE INC. 2016-12-15 US disclosed
US-20160340389-A1 PHARMACEUTICALLY RELEVANT AROMATIC-CATIONIC PEPTIDES STEALTH BIOTHERAPEUTICS INC. 2016-11-24 US disclosed
US-9446059-B2 Carbidopa and L-dopa prodrugs and methods of use ABBVIE INC. (US) 2016-09-20 US disclosed
US-20160106765-A1 Carbidopa and L-Dopa Prodrugs and Methods of Use ABBVIE INC. 2016-04-21 US disclosed
US-8273895-B2 NK1 antagonists OPKO HEALTH, INC. (US) 2012-09-25 US disclosed
US-20120156557-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTE BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2012-06-21 US disclosed
US-20110098468-A1 NK1 ANTAGONISTS OPKO HEALTH, INC. (US) 2011-04-28 US disclosed
EP-2237358-A1 Nonaqueous electrolyte battery MITSUBISHI CHEMICAL CORPORATION (JP) 2010-10-06 EP disclosed
US-20100035147-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTE BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2010-02-11 US disclosed
EP-2128923-A1 NONAQUEOUS ELECTROLYTE SOLUTION AND NONAQUEOUS ELECTROLYTE BATTERY Mitsubishi Chemical Corporation (JP) 2009-12-02 EP disclosed
US-5811575-A HEATING 2-CHLOROETHYLPHOSPHONIC ACIDS CLARIANT GMBH (DE) 1998-09-22 US disclosed
EP-0685484-A2 Process for preparing vinyl phosphonic acids HOECHST AKTIENGESELLSCHAFT (DE) 1995-12-06 EP disclosed
US-4066690-A CHEMICAL INTERMEDIATES FOR PROSTAGLANDINS HOECHST AKTIENGESELLSCHAFT (DT) 1978-01-03 US disclosed
US-3972923-A FROM AN ACYL HALIDE AND A PHOSPHONIC ACID DERIVATIVE HOECHST AKTIENGESELLSCHAFT (DT) 1976-08-03 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 (9 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-20160340389-A1 PHARMACEUTICALLY RELEVANT AROMATIC-CATIONIC PEPTIDES ADM2, VIP, ANPEP CA2 1788/4885CA12 2165/4885MMP2 2491/4885
US-20240217930-A1 SARS-COV-2 MPRO INHIBITOR COMPOUNDS ACE2, SARS1, ACE CA2 2692/4885CA12 4567/4885MMP2 3084/4885
US-20170081363-A1 PHARMACEUTICALLY RELEVANT AROMATIC-CATIONIC PEPTIDES ADM2, VIP, ANPEP CA2 1504/4885CA12 2336/4885MMP2 2197/4885
US-20110098468-A1 NK1 ANTAGONISTS HRH4, CRHR2, HRH2 CA2 2999/4885CA12 4144/4885MMP2 4781/4885
US-20160362431-A1 Carbidopa And L-Dopa Prodrugs And Methods Of Use COMT, SNCA, PARK7 CA2 1712/4885CA12 1587/4885MMP2 969/4885
US-20160106765-A1 Carbidopa and L-Dopa Prodrugs and Methods of Use COMT, SNCA, PARK7 CA2 1712/4885CA12 1587/4885MMP2 969/4885
US-20180208552-A1 UREA DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF FPR1, FPR2, SAAL1 CA2 4424/4885CA12 4870/4885MMP2 4028/4885
US-20240024338-A1 CARBIDOPA AND L-DOPA PRODRUGS AND METHODS OF USE COMT, SNCA, PARK7 CA2 1712/4885CA12 1587/4885MMP2 969/4885
US-20180079762-A1 Carbidopa and L-Dopa Prodrugs and Methods of use COMT, SNCA, PARK7 CA2 1712/4885CA12 1587/4885MMP2 969/4885

“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.