7-Ethyl-10-Hydroxycamptothecin

7-Ethyl-10-Hydroxycamptothecin

SCHEMBL1454961

CCc1c2c(nc3ccc(O)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC.O

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TOP1

The experimentally established mechanism targets of 7-Ethyl-10-Hydroxycamptothecin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
TOP1 known ✓ P11387 17/20 0.75
MEN1 O00255 3/20 0.98
KMT2A Q03164 3/20 0.98
SMN1; SMN2 Q16637 2/20 0.70
CYP3A4 P08684 1/20 0.70
CASP1 P29466 1/20 0.70
CASP7 P55210 1/20 0.70
HBB P68871 1/20 0.70
KDM4E B2RXH2 1/20 0.70
ALDH1A1 P00352 1/20 0.70
HDAC3 O15379 1/20 0.67
HDAC1 Q13547 1/20 0.67
HDAC6 Q9UBN7 1/20 0.67

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
7-Ethyl-10-Hydroxycamptothecin SCHEMBL13420265 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL733477 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL29354078 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL16072280 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL29787648 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL29359781 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL34018 0.99 MEN1 (1.00) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL28292269 0.98 MEN1 (0.98) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL27680702 0.98 MEN1 (0.98) MEN1KMT2ATOP1SMN1; SMN2CYP3A4
7-Ethyl-10-Hydroxycamptothecin SCHEMBL30739326 0.94 MEN1 (0.91) MEN1KMT2ATOP1SMN1; SMN2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7910737-B2 preparation method of 7-ethyl-10-hydroxycamptothecin from 4-ethyl-7,8-dihydro-4-hydroxy-1H-pyrano[3,4-f]indolizine-3,6,10(4H)-trione and 1-(2-amino-5 -hydroxyphenyl)-propan-1-one using higher reaction temperature and faster heating to that temperature in the presence of catalyst FERMION OY (FI) 2011-03-22 US disclosed
EP-1846412-B1 PROCESS FOR THE MANUFACTURING OF 7-ETHYL-10-HYDROXY CAMPTOTHECIN FERMION OY (FI) 2009-10-21 EP disclosed
US-20080103309-A1 Process for the Manufacturing of 7-Ethyl-10-Hydroxy Camptothecin FERMION OY (FI) 2008-05-01 US disclosed
EP-1846412-A1 PROCESS FOR THE MANUFACTURING OF 7-ETHYL-10-HYDROXY CAMPTOTHECIN Fermion Oy (FI) 2007-10-24 EP disclosed
WO-2006082279-A1 PROCESS FOR THE MANUFACTURING OF 7-ETHYL-10-HYDROXY CAMPTOTHECIN FERMION OY (FI) 2006-08-10 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-20080103309-A1 Process for the Manufacturing of 7-Ethyl-10-Hydroxy Camptothecin TOP1, TOP2A, DHPS TOP1 1/4885MEN1 710/4885KMT2A 3520/4885

“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.