SCHEMBL6232779

SCHEMBL6232779

CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2cc3cccc(O)c3nc2-1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TOP1 P11387 18/20 0.77
▸ ALDH1A1 P00352 4/20 0.77
▸ MEN1 O00255 4/20 0.77
▸ KMT2A Q03164 4/20 0.77
▸ SMN1; SMN2 Q16637 4/20 0.77
▸ GLA P06280 3/20 0.77
▸ RECQL P46063 2/20 0.77
▸ TDP1 Q9NUW8 2/20 0.77
▸ KDM4E B2RXH2 4/20 0.76
▸ TP53 P04637 2/20 0.76
▸ HPGD P15428 2/20 0.76
▸ CYP3A4 P08684 2/20 0.76
▸ HBB P68871 2/20 0.76
▸ RAB9A P51151 2/20 0.76
▸ BLM P54132 2/20 0.76
▸ STAT6 P42226 1/20 0.76
▸ CHEK1 O14757 1/20 0.76
▸ HDAC3 O15379 1/20 0.76
▸ ABCC4 O15439 1/20 0.76
▸ GMNN O75496 1/20 0.76

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
SCHEMBL27540723 1.00 TOP1 (0.77) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL8486195 0.91 TOP1 (0.76) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL27547279 0.91 TOP1 (0.76) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL8324984 0.91 TOP1 (0.78) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL7677097 0.90 TOP1 (0.77) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL7263268 0.90 TOP1 (0.75) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL7627096 0.90 TOP1 (0.75) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL7635279 0.89 TOP1 (0.72) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL6367280 0.89 TOP1 (0.78) TOP1ALDH1A1MEN1KMT2ASMN1; SMN2
SCHEMBL6849474 0.89 TOP1 (0.78) TOP1ALDH1A1MEN1KMT2ASMN1; 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 43 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-61085389-A — — None — — JP disclosed
EP-1551371-A2 STABILIZED NANOPARTICLE FORMULATIONS OF CAMPTOTHECA DERIVATIVES Imarx Therapeutics, Inc. (US) 2005-07-13 — — EP disclosed
EP-0963988-B1 Intermediates for making camptothecin and camptothecin analogs UNIV NORTH CAROLINA STATE (US) 2005-04-27 — — EP disclosed
WO-2005007136-A1 METHODS OF MAKING PHARMACEUTICAL FORMULATIONS FOR THE DELIVERY OF DRUGS HAVING LOW AQUEOUS SOLUBILITY IMARX THERAPEUTICS, INC. (US) 2005-01-27 — — WO disclosed
US-20040247624-A1 Methods of making pharmaceutical formulations for the delivery of drugs having low aqueous solubility IMARX THERAPEUTICS, INC. 2004-12-09 — — US disclosed
US-20040009229-A1 Stabilized nanoparticle formulations of camptotheca derivatives IMARX THERAPEUTICS, INC. 2004-01-15 — — US disclosed
WO-2003103596-A2 STABILIZED NANOPARTICLE FORMULATIONS OF CAMPTOTHECA DERIVATIVES IMARX THERAPEUTICS, INC. (US) 2003-12-18 — — WO disclosed
US-20030059465-A1 Stabilized nanoparticle formulations of camptotheca derivatives IMARX THERAPEUTICS, INC. 2003-03-27 — — US disclosed
EP-0982307-B1 9 -Amino- and 9-nitro-camptothecin derivatives, process for their preparation and use as antitumor agents PHARMACIA ITALIA SPA (IT) 2002-12-04 — — EP disclosed
EP-0694035-B1 WATER-SOLUBLE CAMPTOTHECIN DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS ANTITUMOR AGENTS PHARMACIA ITALIA SPA (IT) 2002-07-17 — — EP disclosed
US-5254690-A Alkoxymethylpyridine d-ring intermediates useful for the synthesis of camptpthecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-10-19 — — US disclosed
US-5247089-A Method of making intermediates useful for the manufacture of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-09-21 — — US disclosed
US-5243050-A Alkylpyridone DE ring intermediates useful for the manufacture of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-09-07 — — US disclosed
US-5212317-A Methods and intermediates for the assymmetric synthesis of camptothecin and camptothecin analogs NORTH CAROLINA STATE UNIVERSITY (US) 1993-05-18 — — US disclosed
US-5200524-A Camptothecin intermediates and method of making same NORTH CAROLINA STATE UNIVERSITY (US) 1993-04-06 — — US disclosed
US-5191082-A Camptothecin intermediate and method of making camptothecin intermediates NORTH CAROLINA STATE UNIVERSITY (US) 1993-03-02 — — US disclosed
US-5162532-A INTERMEDIATES AND METHOD OF MAKING CAMPTOTHECIN AND CAMPTOTHECIN ANALOGS NORTH CAROLINA STATE UNIVERSITY (US) 1992-11-10 — — US disclosed
WO-1992011263-A1 METHOD OF MAKING CAMPTOTHECIN AND CAMPTOTHECIN ANALOGS NORTH CAROLINA STATE UNIVERSITY (US) 1992-07-09 — — WO disclosed
JP-S6185389-A NOVEL CAMPTOTHECIN DERIVATIVE YAKULT HONSHA CO LTD 1986-04-30 — — JP disclosed
JP-S06185389-A — — 0001-01-01 — — JP 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-20030059465-A1 Stabilized nanoparticle formulations of camptotheca derivatives PDE8A, LPXN, TOP2A TOP1 5/4885ALDH1A1 1817/4885MEN1 817/4885
US-20040009229-A1 Stabilized nanoparticle formulations of camptotheca derivatives PDE8A, LPXN, TOP2A TOP1 5/4885ALDH1A1 1817/4885MEN1 817/4885
US-20040247624-A1 Methods of making pharmaceutical formulations for the delivery of drugs having low aqueous solubility ACR, LPXN, ABCG2 TOP1 499/4885ALDH1A1 853/4885MEN1 2352/4885

“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.

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