Rubitecan

Rubitecan

SCHEMBL8640

CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2cc3c([N+](=O)[O-])cccc3nc2-1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TOP1

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TOP1 known ✓ P11387 18/20 0.79
ABCC4 O15439 2/20 1.00
HTT P42858 2/20 1.00
ABCC3 O15438 1/20 1.00
ACHE P22303 1/20 1.00
PTGS1 P23219 1/20 1.00
ABCC2 Q92887 1/20 1.00
ALDH1A1 P00352 3/20 0.78
GLA P06280 3/20 0.78
RECQL P46063 2/20 0.78
TDP1 Q9NUW8 2/20 0.78
MEN1 O00255 2/20 0.78
KMT2A Q03164 2/20 0.78
SMN1; SMN2 Q16637 2/20 0.78
KDM4E B2RXH2 3/20 0.77
RAB9A P51151 2/20 0.77
BLM P54132 2/20 0.77
POLB P06746 1/20 0.77
MAPT P10636 1/20 0.77
TP53 P04637 2/20 0.72

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
Rubitecan SCHEMBL29379605 1.00 ABCC4 (1.00) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL29383355 1.00 ABCC4 (1.00) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL6426025 1.00 ABCC4 (1.00) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL15539941 1.00 ABCC4 (1.00) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL1652417 1.00 ABCC4 (1.00) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL28223445 1.00 ABCC4 (1.00) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL27953003 0.98 ABCC4 (0.95) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL28308474 0.96 ABCC4 (0.93) ABCC4HTTABCC3ACHEPTGS1
Rubitecan SCHEMBL27598505 0.94 ABCC3 (0.89) ABCC4HTTABCC3ACHEPTGS1
SCHEMBL25932527 0.92 ABCC4 (0.85) ABCC4HTTABCC3ACHEPTGS1

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

Appears in 23871 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260144890-A1 ANTIBODY DRUG CONJUGATE COMPRISING NMT INHIBITOR CONJUGATED TO AN ANTIBODY MyricX Pharma Limited (GB) 2026-05-28 US claimed
US-20260144882-A1 ANTI-NECTIN-4 ANTIBODY DRUG CONJUGATE AND USE THEREOF BIO-THERA SOLUTIONS, LTD. (CN) 2026-05-28 US claimed
US-20260137794-A1 LIGAND-DRUG CONJUGATE AND USE THEREOF SYSTIMMUNE INC (US) 2026-05-21 US claimed
WO-2026107377-A1 PHARMACOLOGICAL RE-ACTIVATION OF MUTANT PVHL KARANICOLAS JOHN (US) 2026-05-21 WO claimed
EP-4743122-A1 THERAPEUTIC SEALANTS BASED UPON DRUG CONJUGATES The Johns Hopkins University (US) 2026-05-20 EP claimed
WO-2026098633-A1 CONJUGATES AND USES THEREOF CSTONE PHARMACEUTICALS (SUZHOU) CO., LTD. (CN) 2026-05-15 WO claimed
EP-4739310-A1 ECTONUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE 1 (ENPP1) INHIBITOR COMBINATIONS AND USES THEREOF Insilico Medicine IP Limited (HK) 2026-05-13 EP claimed
WO-2026090139-A1 ANTI-LY6K ANTIBODY-DRUG CONJUGATES AND METHODS OF USE NORMUNITY, INC. (US) 2026-04-30 WO claimed
EP-4732850-A1 ANTIBODY-DRUG CONJUGATES AND THEIR USES Antelope Therapeutics SAS (FR) 2026-04-29 EP claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US claimed
US-5922877-A HIGHER YIELD WITHOUT NUMEROUS BYPRODUCTS, USE IN TREATING CANCER THE STEHLIN FOUNDATION FOR CANCER RESEARCH (US) 1999-07-13 US claimed
WO-1999017804-A1 POLYMERIC DERIVATIVES OF CAMPTOTHECINS PHARMACIA & UPJOHN S.P.A. (IT) 1999-04-15 WO claimed
WO-1999015153-A1 SMALL PARTICLE LIPOSOME AEROSOLS FOR DELIVERY OF ANTI-CANCER DRUGS RESEARCH DEVELOPMENT FOUNDATION (US) 1999-04-01 WO claimed
WO-1999007709-A1 METHODS OF PREPARING AND PURIFYING 9-NITRO-20-CAMPTOTHECIN THE STEHLIN FOUNDATION FOR CANCER RESEARCH (US) 1999-02-18 WO claimed
US-5786344-A ADMINISTERING WITH AGENT WHICH INCREASES ACTIVITY OF GLUCURONOSYLTRANSFERASE OR DECREASES ACTIVITY OF BILIARY TRANSPORT PROTEIN ARCH DEVELOPMENT CORPORATION (US) 1998-07-28 US claimed
US-5736156-A ANTICARCINOGENIC AGENT HAVING LACTONE RING PROTECTED FROM HYDROLYSIS BY ASSOCIATION WITH SURFACTANT OR LIPID; DRUG DELIVERY, WATER SOLUBILITY, NONTOXIC THE OHIO STATE UNIVERSITY (US) 1998-04-07 US claimed
EP-0768895-A1 CAMPTOTHECIN DRUG COMBINATIONS AND MEDICAMENTS WITH REDUCED SIDE EFFECTS ARCH DEVELOPMENT CORPORATION (US) 1997-04-23 EP claimed
US-5552156-A ANTITUMOR AGENTS OHIO STATE UNIVERSITY (US) 1996-09-03 US claimed
WO-1996001127-A1 CAMPTOTHECIN DRUG COMBINATIONS AND MEDICAMENTS WITH REDUCED SIDE EFFECTS ARCH DEVELOPMENT CORPORATION (US) 1996-01-18 WO claimed
CN-1113384-A Preparation method of 9-amino camptothecin PHARMACIA SPA (IT) 1995-12-13 CN claimed