SCHEMBL25519261

SCHEMBL25519261

CC(C)NC(=O)O[C@H]1CCn2ccnc21

nearest known ligand 0.37

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CDK2 P24941 10/20 0.37
CCNE1 P24864 9/20 0.37
GRM5 P41594 1/20 0.36
HRH3 Q9Y5N1 1/20 0.34
METAP2 P50579 2/20 0.34
SMYD3 Q9H7B4 1/20 0.33
CYP3A4 P08684 1/20 0.32
TSHR P16473 1/20 0.32
CYP2C19 P33261 1/20 0.32
RET P07949 1/20 0.32
GSK3B P49841 3/20 0.32
KDM4E B2RXH2 1/20 0.32
ALDH1A1 P00352 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
TDP1 Q9NUW8 1/20 0.32

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
SCHEMBL20998179 0.86 CHRM1 (0.38) GRM5KDM4E
SCHEMBL25519258 0.81 GAA (0.33) CDK2CCNE1GSK3BSMN1; SMN2
SCHEMBL19220264 0.81 GAA (0.33) CDK2CCNE1GSK3BSMN1; SMN2
SCHEMBL25519241 0.81 CHRM2 (0.34) TSHRKDM4E
SCHEMBL19220263 0.81 CHRM2 (0.34) TSHRKDM4E
SCHEMBL25519244 0.78 KMT2A (0.41) SMN1; SMN2TDP1
SCHEMBL25519256 0.77 ACKR3 (0.36) CDK2CCNE1HRH3GSK3B
SCHEMBL19220286 0.77 DRD3 (0.35) KDM4EALDH1A1
SCHEMBL25519260 0.76 EPHX1 (0.36) ALDH1A1
SCHEMBL25519257 0.75 HSD11B1 (0.41) HRH3TSHRKDM4EALDH1A1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11655255-B2 Method for catalytic asymmetric synthesis of phosphorus-stereogenic (P-stereogenic) nucleoside derivative and catalyst used therein SPH NO.1 BIOCHEMICAL & PHARMACEUTICAL CO., LTD. (CN) 2023-05-23 US disclosed
US-11655255-B2 Method for catalytic asymmetric synthesis of phosphorus-stereogenic (P-stereogenic) nucleoside derivative and catalyst used therein SPH NO.1 BIOCHEMICAL & PHARMACEUTICAL CO., LTD. (CN) 2023-05-23 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-11655255-B2 Method for catalytic asymmetric synthesis of phosphorus-stereogenic (P-stereogenic) nucleoside derivative and catalyst used therein PNP, TYMP, MTAP CDK2 710/4885CCNE1 2379/4885GRM5 4379/4885

“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.