SCHEMBL6467580

SCHEMBL6467580

C=CI.CCC1CCOO1

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
SCHEMBL5945065 0.87
SCHEMBL27626915 0.84
Bromide SCHEMBL3286869 0.82
SCHEMBL8196755 0.73
SCHEMBL2087261 0.71
Methyl Alcohol SCHEMBL20875603 0.70
SCHEMBL4612501 0.69
SCHEMBL9050980 0.67
Acetic Acid SCHEMBL16872541 0.66 HPGD (0.31)
SCHEMBL14678020 0.65

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6867305-B2 Synthesis of epothilones, intermediates thereto and analogues thereof SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 2005-03-15 US disclosed
EP-1259490-A2 SYNTHESIS OF EPOTHILONES, INTERMEDIATES THERETO AND ANALOGUES THEREOF Sloan Kettering Institute For Cancer Research (US) 2002-11-27 EP disclosed
US-20020058286-A1 Synthesis of epothilones, intermediates thereto and analogues thereof NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2002-05-16 US disclosed
US-20020058817-A1 Synthesis of epothilones, intermediates thereto and analogues thereof NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2002-05-16 US disclosed
WO-2001064650-A2 SYNTHESIS OF EPOTHILONES, INTERMEDIATES THERETO AND ANALOGUES THEREOF SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH CENTER (US) 2001-09-07 WO disclosed