SCHEMBL1659286

SCHEMBL1659286

CC1CC=CC(O)C1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL10306744 1.00
SCHEMBL10306745 1.00
SCHEMBL13181353 1.00
SCHEMBL14565097 0.79
SCHEMBL15037741 0.73
SCHEMBL17190512 0.73 NPC1 (0.32)
SCHEMBL790100 0.72
SCHEMBL789871 0.72
SCHEMBL790770 0.72
SCHEMBL720112 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1233666-C Method for preparing stable photochromic latexes, latexes obtained and use in ophthalmic optics ESSILOR INT (FR) 2005-12-28 CN claimed
CN-1531556-A Method for obtaining stabilised photochromic latex, latex obtained and use in ophthalmic optics �����չ���ͨ�ù�ѧ��˾ 2004-09-22 CN claimed
EP-2438078-B1 NOVOBIOCIN ANALOGUES HAVING MODIFIED SUGAR MOIETIES UNIV KANSAS (US) 2017-10-25 EP disclosed
US-9120774-B2 Novobiocin analogues having modified sugar moieties UNIVERSITY OF KANSAS (US) 2015-09-01 US disclosed
US-9120774-B2 Novobiocin analogues having modified sugar moieties UNIVERSITY OF KANSAS (US) 2015-09-01 US disclosed
US-8632792-B2 Cooling sensation agent composition and sensory stimulation agent composition TAKASAGO INTERNATIONAL CORPORATION (JP) 2014-01-21 US disclosed
US-20130131169-A1 COOLING SENSATION AGENT COMPOSITION, SENSORY STIMULATION AGENT COMPOSITION AND USE OF THE SAME TAKASAGO INTERNATIONAL CORPORATION (JP) 2013-05-23 US disclosed
US-8377458-B2 Cooling sensation agent composition, sensory stimulation agent composition and use of the same TAKASAGO INTERNATIONAL CORPORATION (JP) 2013-02-19 US disclosed
US-20120252745-A1 NOVOBIOCIN ANALOGUES HAVING MODIFIED SUGAR MOIETIES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2012-10-04 US disclosed
US-20120252745-A1 NOVOBIOCIN ANALOGUES HAVING MODIFIED SUGAR MOIETIES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2012-10-04 US disclosed
US-8212012-B2 Novobiocin analogues having modified sugar moieties UNIVERSITY OF KANSAS (US) 2012-07-03 US disclosed
CN-1216917-C Resin for printing ink and printing ink TOYO INK CO LTD (JP) 2005-08-31 CN disclosed
CN-1531556-A Method for obtaining stabilised photochromic latex, latex obtained and use in ophthalmic optics �����չ���ͨ�ù�ѧ��˾ 2004-09-22 CN disclosed
CN-1146535-C Preparing method for azide derivatives 卫材株式会社 2004-04-21 CN disclosed
CN-1326472-A Resin for printing ink and printing ink TOYO INK MFG CO (JP) 2001-12-12 CN disclosed
CN-1194264-A Preparing method for azide derivatives EISAI CO LTD (JP) 1998-09-30 CN disclosed
CN-1060290-A The asymmetric Epoxidation method of chiral hydroperoxide ARCO CHEM TECH (US) 1992-04-15 CN disclosed
US-4725628-A Process of making a crosslinked superabsorbent polyurethane foam KIMBERLY-CLARK CORPORATION (US) 1988-02-16 US disclosed
US-4250964-A INJECTING CYCLOHEXENE OR CYCLOHEXADIENE TO REDUCE VISCOSITY GULF RESEARCH & DEVELOPMENT COMPANY (US) 1981-02-17 US disclosed
US-4105697-A Process for the preparation of α, β-ethylenic aldehydes RHONE-POULENC INDUSTRIES (FR) 1978-08-08 US disclosed