SCHEMBL6661490

SCHEMBL6661490

C[C@@H]1C[C@H](O)[C@H](C)C[C@@H]1O

nearest known ligand 0.42

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA4 P22748 1/20 0.42
FUCA1 P04066 9/20 0.36
TRPA1 O75762 2/20 0.32
TRPM8 Q7Z2W7 2/20 0.32
MAPT P10636 1/20 0.31
FUCA2 Q9BTY2 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
SCHEMBL3680381 1.00 CA1 (0.42) CA1CA2CA4FUCA1TRPA1
SCHEMBL16672067 1.00 CA1 (0.42) CA1CA2CA4FUCA1TRPA1
SCHEMBL6660696 1.00 CA1 (0.42) CA1CA2CA4FUCA1TRPA1
SCHEMBL14139975 0.93 CA1 (0.38) CA1CA2CA4FUCA1
SCHEMBL4444833 0.93 CA1 (0.38) CA1CA2CA4FUCA1
SCHEMBL12675735 0.91
SCHEMBL46095 0.91
SCHEMBL5586362 0.91
SCHEMBL684418 0.91
SCHEMBL5586361 0.91

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1030854-B1 CATALYSTS FOR ASYMMETRIC SYNTHESIS CONTAINING RIGID CHIRAL LIGANDS PENN STATE RES FOUND (US) 2004-08-18 EP disclosed
US-6399787-B1 TRANSITION METAL COMPLEX PENN STATE RESEARCH FOUNDATION 2002-06-04 US disclosed
US-6380416-B2 CHIRAL BIDENTATE PHOSPHINE LIGANDS WITH CYCLIC RINGS TO RESTRICT CONFORMATIONAL FLEXIBILITY OF THE LIGANDS TO ENHANCE EFFICIENCY; STEREOSELECTIVE HYDROGENATION OF KETONES TO ALCOHOLS, AND A-ACETOAMIDOCINNAMIC ACID TO ACYLAMINO ACIDS THE PENN STATE RESEARCH FOUNDATION 2002-04-30 US disclosed
US-20010047113-A1 Chiral bidentate phosphine ligands with cyclic rings to restrict conformational flexibility of the ligands to enhance efficiency; stereoselective hydrogenation of ketones to alcohols, and a-acetoamidocinnamic acid to acylamino acids THE PENN STATE RESEARCH FOUNDATION 2001-11-29 US disclosed
US-6278024-B1 AS CATALYSTS FOR ASSYMETRIC SYNTHESIS THE PENN STATE RESEARCH FOUNDATION 2001-08-21 US disclosed
US-6207868-B1 BASED ON CHIRAL BIDENTATE PHOSPHINE LIGANDS WITH CYCLIC RING STRUCTURES TO RESTRICT CONFORMATIONAL FLEXIBILITY, ASYMMETRIC SYNTHESIS OF ALCOHOLS BY ENANTIOSELECTIVE HYDROGENATION OF KETONES CATALYZED BY THE CHIRAL LIGANDS THE PENN STATE RESEARCH FOUNDATION 2001-03-27 US disclosed
WO-1999059721-A1 CATALYTIC ASYMMETRIC HYDROGENATION, HYDROFORMYLATION, AND HYDROVINYLATION VIA TRANSITION METAL CATALYSTS WITH PHOSPHINES AND PHOSPHITES THE PENN STATE RESEARCH FOUNDATION (US) 1999-11-25 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-20010047113-A1 Chiral bidentate phosphine ligands with cyclic rings to restrict conformational flexibility of the ligands to enhance efficiency; stereoselective hydrogenation of ketones to alcohols, and a-acetoamidocinnamic acid to acylamino acids ADH1A, AASDHPPT, AADAT CA1 114/4885CA2 300/4885CA4 187/4885

“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.