SCHEMBL5652672

SCHEMBL5652672

CCOC(=O)CN1C2CC(OC3CCCCO3)CC1CC(C(=O)OCC)C2.CS(=O)(=O)O

nearest known ligand 0.34

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.34
KMT2A Q03164 2/20 0.34
ALDH1A1 P00352 6/20 0.33
POLB P06746 2/20 0.33
SMN1; SMN2 Q16637 3/20 0.31
TP53 P04637 1/20 0.31
CYP3A4 P08684 1/20 0.31
MAPK1 P28482 1/20 0.31
CYP2C19 P33261 1/20 0.31
HPGD P15428 1/20 0.31
HTT P42858 1/20 0.30
RCE1 Q9Y256 1/20 0.30
KDM4E B2RXH2 2/20 0.30
L3MBTL1 Q9Y468 1/20 0.30
TSHR P16473 1/20 0.30
RAB9A P51151 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
SCHEMBL8849456 0.95 MEN1 (0.37) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL8849464 0.87 MEN1 (0.37) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL4482763 0.82 ALDH1A1 (0.32) ALDH1A1SMN1; SMN2CYP3A4
SCHEMBL14891097 0.81 MEN1 (0.43) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL14441116 0.77 ALDH1A1 (0.30) ALDH1A1
SCHEMBL2016829 0.74 ALDH1A1 (0.44) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL8912197 0.73 KMT2A (0.45) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL5653075 0.73 ALDH1A1 (0.39) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL30028689 0.73 MEN1 (0.43) MEN1KMT2AALDH1A1POLBSMN1; SMN2
SCHEMBL5114769 0.72 MEN1 (0.40) MEN1KMT2AALDH1A1POLBCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070299260-A1 Method for Preparing Hexahydro-8-Hydroxy-2, 6-Methano-2H-Chinolizin-3 (4H) -One Esters CILAG LTD. (CH) 2007-12-27 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 (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-20070299260-A1 Method for Preparing Hexahydro-8-Hydroxy-2, 6-Methano-2H-Chinolizin-3 (4H) -One Esters CYP4Z1, HDHD5, HCAR2 MEN1 2258/4885KMT2A 1047/4885ALDH1A1 541/4885

“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.