SCHEMBL10194129

SCHEMBL10194129

CCCCOc1cc(CO)on1

nearest known ligand 0.51

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
SMPD1 P17405 2/20 0.51
ALDH1A1 P00352 1/20 0.43
HRH3 Q9Y5N1 1/20 0.42
CYP19A1 P11511 2/20 0.42
CYP1A2 P05177 1/20 0.42
CYP2C9 P11712 1/20 0.42
CYP2C19 P33261 1/20 0.42
NOTUM Q6P988 2/20 0.41

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
SCHEMBL5887797 0.91 SMPD1 (0.46) SMPD1ALDH1A1HRH3NOTUM
SCHEMBL14228524 0.86 SMPD1 (0.47) SMPD1ALDH1A1HRH3CYP19A1CYP1A2
SCHEMBL26928299 0.84 NOTUM (0.44) SMPD1ALDH1A1NOTUM
SCHEMBL6128431 0.83 SMPD1 (0.44) SMPD1ALDH1A1HRH3CYP19A1CYP1A2
SCHEMBL10288677 0.80 SMPD1 (0.43) SMPD1ALDH1A1HRH3CYP19A1CYP1A2
SCHEMBL11923794 0.79 SMPD1 (0.42) SMPD1ALDH1A1HRH3CYP19A1CYP1A2
SCHEMBL7303479 0.79 NOTUM (0.43) HRH3NOTUM
SCHEMBL25602002 0.77 SMPD1 (0.47) SMPD1ALDH1A1CYP19A1CYP1A2CYP2C9
SCHEMBL15871987 0.77 SMPD1 (0.48) SMPD1ALDH1A1CYP19A1CYP1A2CYP2C9
SCHEMBL17122452 0.76 SMPD1 (0.43) SMPD1ALDH1A1HRH3CYP19A1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3138831-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF President and Fellows of Harvard College (US) 2017-03-08 EP disclosed
US-20160340325-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2016-11-24 US disclosed
EP-3056487-A1 SYNTHESIS OF ENONE INTERMEDIATE President and Fellows of Harvard College (US) 2016-08-17 EP disclosed
US-9365493-B2 Synthesis of tetracyclines and analogues thereof PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2016-06-14 US disclosed
EP-2487160-B1 Synthesis of Enone Intermediate HARVARD COLLEGE (US) 2016-02-03 EP disclosed
EP-2590944-B1 1-PHENYL-SUBSTITUTED HETEROCYCLYL DERIVATIVES AND THEIR USE AS PROSTAGLANDIN D2 RECEPTOR MODULATORS ACTELION PHARMACEUTICALS LTD (CH) 2015-09-30 EP disclosed
US-8907104-B2 Synthesis of enone intermediate PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2014-12-09 US disclosed
EP-2479169-B1 Synthesis of Enone Intermediate HARVARD COLLEGE (US) 2014-12-03 EP disclosed
US-20140179929-A1 SYNTHESIS OF ENONE INTERMEDIATE PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2014-06-26 US disclosed
US-20140163238-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2014-06-12 US disclosed
EP-2479169-A1 Synthesis of Enone Intermediate President and Fellows of Harvard College (US) 2012-07-25 EP disclosed
US-20120029199-A1 SYNTHESIS OF ENONE INTERMEDIATE PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2012-02-02 US disclosed
US-7960559-B2 Synthesis of enone intermediate PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2011-06-14 US disclosed
US-20110009639-A1 SYNTHESIS OF ENONE INTERMEDIATE MYERS ANDREW G 2011-01-13 US disclosed
US-20110009371-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2011-01-13 US disclosed
US-7807842-B2 Synthesis of tetracyclines and analogues thereof PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2010-10-05 US disclosed
US-7763735-B2 modular synthesis of tetracycline analogs through a chiral enone intermediate; efficiency PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2010-07-27 US disclosed
US-20100130451-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF PRESIDENTS AND FELLOWS OF HARVARD COLLEGE (US) 2010-05-27 US disclosed
US-20090093640-A1 modular synthesis of tetracycline analogs through a chiral enone intermediate; efficiency NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2009-04-09 US disclosed
WO-2008127361-A2 SYNTHESIS OF ENONE INTERMEDIATE PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2008-10-23 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 (8 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-20140163238-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF TET1, TET3, MYC SMPD1 4444/4885ALDH1A1 4455/4885HRH3 3556/4885
US-20110009639-A1 SYNTHESIS OF ENONE INTERMEDIATE TECR, ECI1, ERAL1 SMPD1 4418/4885ALDH1A1 3547/4885HRH3 4112/4885
US-20090093640-A1 modular synthesis of tetracycline analogs through a chiral enone intermediate; efficiency TECR, TSN, TARS2 SMPD1 4683/4885ALDH1A1 4307/4885HRH3 4077/4885
US-20100130451-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF CCNE1, CCNE2, CCNT2 SMPD1 4492/4885ALDH1A1 4622/4885HRH3 3897/4885
US-20110009371-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF TET1, TET3, MYC SMPD1 4444/4885ALDH1A1 4455/4885HRH3 3556/4885
US-20140179929-A1 SYNTHESIS OF ENONE INTERMEDIATE TECR, ECI1, ERAL1 SMPD1 4418/4885ALDH1A1 3547/4885HRH3 4112/4885
US-20120029199-A1 SYNTHESIS OF ENONE INTERMEDIATE TECR, ECI1, ERAL1 SMPD1 4418/4885ALDH1A1 3547/4885HRH3 4112/4885
US-20160340325-A1 SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF TET1, TET3, MYC SMPD1 4444/4885ALDH1A1 4455/4885HRH3 3556/4885

“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.