Carmustine

Carmustine

SCHEMBL4503

O=NN(CCCl)C(=O)NCCCl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GSR

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

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
GSR known ✓ P00390 1/20 1.00
ALDH1A1 P00352 2/20 1.00
BLM P54132 2/20 1.00
PMP22 Q01453 2/20 1.00
MEN1 O00255 1/20 1.00
ABCB11 O95342 1/20 1.00
TSHR P16473 1/20 1.00
HTT P42858 1/20 1.00
KMT2A Q03164 1/20 1.00
ADRA2A P08913 2/20 0.53
PDE4A P27815 1/20 0.53
ADRA1A P35348 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.49
LMNA P02545 1/20 0.45
NFKB1 P19838 1/20 0.45
EGFR P00533 3/20 0.32
ERBB2 P04626 3/20 0.32
FAAH O00519 1/20 0.32

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
Carmustine SCHEMBL2047318 1.00 ALDH1A1 (1.00) ALDH1A1BLMPMP22MEN1ABCB11
Carmustine SCHEMBL5783727 0.94 ALDH1A1 (0.89) ALDH1A1BLMPMP22MEN1ABCB11
Elmustine SCHEMBL93476 0.90 ALDH1A1 (0.82) ALDH1A1BLMPMP22MEN1ABCB11
SCHEMBL20906025 0.90 ALDH1A1 (0.82) ALDH1A1BLMPMP22MEN1ABCB11
SCHEMBL9856739 0.87 BLM (0.76) ALDH1A1BLMPMP22MEN1ABCB11
SCHEMBL25309077 0.87 ALDH1A1 (0.77) ALDH1A1BLMPMP22MEN1ABCB11
SCHEMBL19351409 0.87 ALDH1A1 (0.77) ALDH1A1BLMPMP22MEN1ABCB11
SCHEMBL9856483 0.87 ALDH1A1 (0.77) ALDH1A1BLMPMP22MEN1ABCB11
SCHEMBL10005923 0.87 ALDH1A1 (0.77) ALDH1A1BLMPMP22MEN1ABCB11
Ditiomustine SCHEMBL607073 0.85 ALDH1A1 (0.74) ALDH1A1BLMPMP22MEN1ABCB11

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 159129 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4748859-A2 CHEMICALLY AND PHOTOCHEMICALLY INITIATED CELL MEMBRANE BLEBBING TO INDUCE CELL VESICLE PRODUCTION, MODIFICATIONS THEREOF, AND USES THEREOF The Regents of the University of California (US) 2026-05-27 EP claimed
CN-116209439-B Cereblon protein modulators Saint Jude Children's Research Hospital Ltd. (US) 2026-05-26 CN claimed
WO-2026107377-A1 PHARMACOLOGICAL RE-ACTIVATION OF MUTANT PVHL KARANICOLAS JOHN (US) 2026-05-21 WO claimed
US-20260137700-A1 PHARMACEUTICAL COMBINATION OF PRMT5 INHIBITOR AND DNA DAMAGE-INDUCING SUBSTANCE SK BIOPHARMACEUTICALS CO LTD (KR) 2026-05-21 US claimed
WO-2026102563-A1 DISUBSTITUTED PYRIMIDOPYRROLE ANALOG AND USE THEREOF 深圳湾实验室坪山生物医药研发转化中心 2026-05-21 WO claimed
US-20260139071-A1 Subcutaneous Formulations Of Anti-CD38 Antibodies And Their Uses JANSSEN BIOTECH INC (US) 2026-05-21 US claimed
US-20260137650-A1 MODULATORS OF RAR RELATED ORPHAN RECEPTORS (RORs) 11949098 CANADA INC (CA) 2026-05-21 US claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
EP-4743490-A1 HUMANIZED ANTI-CD7 ANTIBODY Christian-Albrechts-Universität zu Kiel (DE) 2026-05-20 EP claimed
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
EP-0335966-A4 VASOCONSTRICTIVE SUBSTANCES IN COMBINATION WITH CYTOTOXIC AGENTS. MATRIX PHARMA INC (US) 1990-02-20 EP claimed
EP-0349617-A1 METHOD FOR DETECTING IMMUNE-MEDIATED CYTOTOXICITY ONCOTECH INCORPORATED (US) 1990-01-10 EP claimed
EP-0335966-A1 VASOCONSTRICTIVE SUBSTANCES IN COMBINATION WITH CYTOTOXIC AGENTS MATRIX PHARMACEUTICALS, INC. (US) 1989-10-11 EP claimed
WO-1989006162-A1 METHODS AND APPARATUS ASSESSING TUMOR RESISTANCE ONCOTECH INCORPORATED (US) 1989-07-13 WO claimed
WO-1989003995-A1 METHOD FOR DETECTING IMMUNE-MEDIATED CYTOTOXICITY ONCOTECH INCORPORATED (US) 1989-05-05 WO claimed
WO-1989002734-A1 VASOCONSTRICTIVE SUBSTANCES IN COMBINATION WITH CYTOTOXIC AGENTS MATRIX PHARMACEUTICALS, INC. (US) 1989-04-06 WO claimed
EP-0227593-A1 Use of chelating agents THE HOSPITAL FOR SICK CHILDREN (CA) 1987-07-01 EP claimed
US-4600573-A ANTITUMOR AGENTS RESEARCH CORPORATION (US) 1986-07-15 US claimed
US-4300557-A Method for treating intraocular malignancies THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1981-11-17 US claimed
US-4028410-A Process of preparing 1,3-bis(2-chloroethyl)-1-nitrosourea THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH, EDUCATION AND WELFARE (US) 1977-06-07 US claimed