SCHEMBL25839860

SCHEMBL25839860

Nc1cnc2cccc(Cl)c2c1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR4A2 P43354 3/20 0.41
CYP1A2 P05177 1/20 0.39
CYP2A6 P11509 1/20 0.39
PDE3B Q13370 1/20 0.38
PDE3A Q14432 1/20 0.38
EGFR P00533 2/20 0.38
ERBB2 P04626 1/20 0.38
NPC1 O15118 2/20 0.38
RAB9A P51151 2/20 0.38
FGFR1 P11362 1/20 0.37
SRC P12931 1/20 0.37
NOS1 P29475 1/20 0.36
PRMT5 O14744 1/20 0.36
KDM4E B2RXH2 1/20 0.35
GPR3 P46089 1/20 0.35
CHEK1 O14757 1/20 0.35
FLT3 P36888 1/20 0.35
PLK3 Q9H4B4 1/20 0.35
MAP4K4 O95819 1/20 0.35
HAVCR2 Q8TDQ0 1/20 0.35

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
SCHEMBL29990013 1.00 NR4A2 (0.41) NR4A2CYP1A2CYP2A6PDE3BPDE3A
Isopropyl Alcohol SCHEMBL28293164 0.90 NPC1 (0.36) NR4A2PDE3BPDE3AEGFRERBB2
SCHEMBL4879213 0.80 PDE3B (0.44) NR4A2CYP1A2CYP2A6PDE3BPDE3A
SCHEMBL27997404 0.80 ALDH1A1 (0.50) NR4A2CYP1A2NPC1RAB9AKDM4E
SCHEMBL25245129 0.77 PDGFRB (0.51) EGFRNPC1RAB9AKDM4EGPR3
SCHEMBL18318196 0.77 SMN1; SMN2 (0.44) CYP1A2CYP2A6PDE3BPDE3ANPC1
SCHEMBL15034693 0.77 CYP1A2 (0.39) CYP1A2CYP2A6PDE3BPDE3AEGFR
SCHEMBL14405531 0.77 CYP1A2 (0.50) NR4A2CYP1A2CYP2A6PDE3BPDE3A
SCHEMBL28495811 0.77 BACE1 (0.47) EGFRERBB2NPC1RAB9AFGFR1
SCHEMBL11167720 0.77 CYP1A2 (0.39) CYP1A2CYP2A6PDE3BPDE3ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250059196-A1 TRICYCLIC DERIVATIVE INHIBITOR, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2025-02-20 US disclosed
EP-4458819-A1 TRICYCLIC DERIVATIVE INHIBITOR, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF Shanghai Hansoh Biomedical Co., Ltd. (CN) 2024-11-06 EP disclosed
CN-118451068-A Tri-fused ring derivative inhibitor, preparation method and application thereof 上海翰森生物医药科技有限公司 2024-08-06 CN disclosed
WO-2023125877-A1 TRICYCLIC DERIVATIVE INHIBITOR, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 上海翰森生物医药科技有限公司 2023-07-06 WO disclosed
WO-2023125877-A1 TRICYCLIC DERIVATIVE INHIBITOR, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 上海翰森生物医药科技有限公司 2023-07-06 WO disclosed
CN-116375683-A Diazole derivative inhibitor, preparation method and application thereof 上海翰森生物医药科技有限公司 2023-07-04 CN 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-20250059196-A1 TRICYCLIC DERIVATIVE INHIBITOR, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF WEE1, CYP51A1, WEE2 NR4A2 4171/4885CYP1A2 336/4885CYP2A6 297/4885

“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.