Anagrelide

Anagrelide

SCHEMBL1027237

O=C1CN2Cc3c(ccc(Cl)c3Cl)N=C2N1.O=c1[nH]cc(F)c(=O)[nH]1

nearest known ligand 0.71

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PDE3APDE3B

The experimentally established mechanism targets of Anagrelide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PDE3B known ✓ Q13370 19/20 0.71
PDE3A known ✓ Q14432 19/20 0.71
P2RY12 Q9H244 2/20 0.71
MEN1 O00255 1/20 0.71
PDE2A O00408 1/20 0.71
KMT2A Q03164 1/20 0.71
ALDH1A1 P00352 1/20 0.40
LMNA P02545 1/20 0.40
MAPT P10636 1/20 0.40
CYP19A1 P11511 1/20 0.40
TSHR P16473 1/20 0.40
THPO P40225 1/20 0.40
MTOR P42345 1/20 0.40
HTT P42858 1/20 0.40
HBB P68871 1/20 0.40
PMP22 Q01453 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40

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
Anagrelide SCHEMBL29491059 0.84 PDE3B (1.00) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL5060881 0.84 PDE3B (1.00) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL9411 0.84 PDE3B (1.00) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL318593 0.83 PDE3B (0.97) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL9046734 0.83 PDE3B (0.97) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL1449704 0.83 PDE3B (0.97) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL1568712 0.83 PDE3B (0.97) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL729172 0.82 PDE3B (0.94) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL16335881 0.79 PDE3B (0.87) PDE3BPDE3AP2RY12MEN1PDE2A
Anagrelide SCHEMBL1664162 0.78 PDE3B (0.85) PDE3BPDE3AP2RY12MEN1PDE2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210252004-A1 USE OF SODIUM CHANNEL BLOCKERS FOR THE TREATMENT OF NEUROPATHIC PAIN DEVELOPING AS A CONSEQUENCE OF CHEMOTHERAPY WEX MEDICAL LIMITED (HK) 2021-08-19 US disclosed
EP-2274010-A1 THERAPEUTIC COMBINATIONS OF ANTI-IGF-1R ANTIBODIES AND OTHER COMPOUNDS Biogen Idec MA Inc. (US) 2011-01-19 EP disclosed
WO-2009126304-A1 THERAPEUTIC COMBINATIONS OF ANTI-IGF-1R ANTIBODIES AND OTHER COMPOUNDS BIOGEN IDEC MA INC. (US) 2009-10-15 WO 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-20210252004-A1 USE OF SODIUM CHANNEL BLOCKERS FOR THE TREATMENT OF NEUROPATHIC PAIN DEVELOPING AS A CONSEQUENCE OF CHEMOTHERAPY SCN10A, SCN5A, SCN3A PDE3B 1289/4885PDE3A 1101/4885P2RY12 481/4885

“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.