SCHEMBL5510072

SCHEMBL5510072

CC(C)(C)OC(=O)N1CCc2[nH]c3c(N)cccc3c2C1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
F12 P00748 3/20 0.47
NR1H2 P55055 1/20 0.46
BAZ2B Q9UIF8 3/20 0.46
LMNA P02545 2/20 0.46
MAPT P10636 2/20 0.46
CFTR P13569 2/20 0.44
HDAC1 Q13547 1/20 0.43
HDAC6 Q9UBN7 1/20 0.43
PABPC1 P11940 1/20 0.43
ATM Q13315 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
ESR2 Q92731 1/20 0.42
ADORA1 P30542 1/20 0.42
MAPK1 P28482 1/20 0.41
DDB1 Q16531 1/20 0.41
CRBN Q96SW2 1/20 0.41
KDM4E B2RXH2 1/20 0.41
CGAS Q8N884 1/20 0.41
PARP1 P09874 1/20 0.41
TNKS2 Q9H2K2 1/20 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
SCHEMBL21154244 0.87 CFTR (0.56) F12NR1H2BAZ2BLMNAMAPT
SCHEMBL1841280 0.87 LMNA (0.46) F12NR1H2BAZ2BLMNAMAPT
SCHEMBL2244149 0.85 CTSK (0.52) F12NR1H2BAZ2BLMNAMAPT
SCHEMBL1845995 0.85 CTSK (0.51) F12NR1H2BAZ2BLMNAMAPT
SCHEMBL1843650 0.85 CTSK (0.51) F12BAZ2BLMNAMAPTCFTR
SCHEMBL5512666 0.84 MAPT (0.53) F12BAZ2BLMNAMAPTCFTR
SCHEMBL2241936 0.81 MAPT (0.69) BAZ2BLMNAMAPTCFTRPABPC1
SCHEMBL29357331 0.81 MAPT (0.69) BAZ2BLMNAMAPTCFTRPABPC1
SCHEMBL4791778 0.80 CGAS (0.45) F12NR1H2BAZ2BLMNAMAPT
SCHEMBL5511793 0.80 LMNA (0.51) F12BAZ2BLMNAMAPTCFTR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE39680-E1 Substituted heterocycle fused gamma-carbolines BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2007-06-05 US disclosed
US-7183282-B2 Substituted heterocycle fused γ-carbolines BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2007-02-27 US disclosed
US-20060148808-A1 Substituted heterocycle fused gamma-carbolines BRISTOL-MYERS SQUIBB PHARMA COMPANY 2006-07-06 US disclosed
US-7071186-B2 Substituted heterocycle fused gamma-carbolines BRISTOL-MYERS SQUIBB PHARMA CO. (US) 2006-07-04 US disclosed
US-20040220178-A1 Substituted heterocycle fused gamma-carbolines BRISTOL-MYERS SQUIBB PHARMA COMPANY 2004-11-04 US disclosed
EP-1189904-B1 SUBSTITUTED HETEROCYCLE FUSED GAMMA-CARBOLINES BRISTOL MYERS SQUIBB PHARMA CO (US) 2004-09-22 EP disclosed
US-20040034015-A1 Substituted heterocycle fused gamma-carbolines ROBICHAUD ALBERT J (US) 2004-02-19 US disclosed
US-6552017-B1 As serotonin agonists and antagonists and are useful in the control or prophylaxis of central nervous system disorders including obesity, anxiety, depression, psychosis, schizophrenia, sleep disorders, sexual disorders, migraine BRISTOL-MYERS SQUIBB PHARMA COMPANY 2003-04-22 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 (3 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-20040034015-A1 Substituted heterocycle fused gamma-carbolines HCRTR1, HTR2C, OPRK1 F12 1051/4885NR1H2 294/4885BAZ2B 1689/4885
US-20060148808-A1 Substituted heterocycle fused gamma-carbolines HTR2B, HTR1B, HTR3B F12 690/4885NR1H2 302/4885BAZ2B 1007/4885
US-20040220178-A1 Substituted heterocycle fused gamma-carbolines HCRTR1, HTR2C, OPRK1 F12 1051/4885NR1H2 294/4885BAZ2B 1689/4885

“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.