ADC TOXICITY ATLAS
Payloads & linkers
Payload · Maytansinoid

Lys-SMCC-DM1

Tubulin inhibitor

CC1C2CC(C(C=CC=C(CC3=CC(=C(C(=C3)OC)Cl)N(C(=O)CC(C4(C1O4)C)OC(=O)C(C)N(C)C(=O)CCSC5CC(=O)N(C5=O)CC6CCC(CC6)C(=O)NCCCCC(C(=O)O)N)C)C)OC)(NC(=O)O2)O
Physicochemistry

Properties

MW
1103.7 Da
XLogP3
-0.2
logD₇.₄
-0.5
TPSA
312 Ų
pKa
2.2
Charge pH 7.4
Zwitterion
H-bond donors
5
H-bond acceptors
17
Bystander
No
PubChem CID
74832310
Bioactivity
ADCdb lists T-DM1 cellular IC50 values spanning ~0.04 nM (high HER2-expressing lines) to >500 nM (low/negative HER2 lines), HER2-expression dependent. No isolated free-payload (DM1) IC50 is given on the ADCdb ADC page; DM1 is a potent antimitotic maytansinoid that inhibits tubuli
4 agents

ADCs built on this payload

Agent · target
Ocular
Hepatic
Neutrop.
Thrombo.
Anemia
GI
ILD
Neuro.
AMG-224TNFRSF17
30
45.5
27.3
72.7
27.3
36.4
9.1
AVID-100EGFR
8
20
24
4
32
Trastuzumab emtansineERBB2
5
98
39
83
60
40
1.2
21
Lorvotuzumab mertansineNCAM1
4.7
16.5
30.9
17.5
0%severity100%
0
Assessed · clear
true 0%
No data
never assessed