ChemicalBook >> CAS DataBase List >>AT-406(AT406)

AT-406(AT406)

CAS No.
1071992-99-8
Chemical Name:
AT-406(AT406)
Synonyms
Xevinapant;SM 406;QCR-136;Debio-1143;SureCN2724374;AT-406(AT406);CHEMBL2158051;AT-406 (SM-406);AT-406(Xevinapant);Xevinapant (AT406)
CBNumber:
CB92630066
Molecular Formula:
C32H43N5O4
Molecular Weight:
561.71
MDL Number:
MFCD22124467
MOL File:
1071992-99-8.mol
Last updated:2023-06-08 09:02:45

AT-406(AT406) Properties

Boiling point 840.6±65.0 °C(Predicted)
Density 1.21
storage temp. Store at -20°C
solubility ≥27.65 mg/mL in DMSO; insoluble in H2O; ≥27 mg/mL in EtOH
form solid
pka 13.65±0.40(Predicted)
InChIKey LSXUTRRVVSPWDZ-MKKUMYSQSA-N
SMILES N12[C@H](C(NC(C3=CC=CC=C3)C3=CC=CC=C3)=O)CC[C@]1([H])CCN(C(=O)CC(C)C)C[C@H](NC(=O)[C@@H](NC)C)C2=O
FDA UNII N65WC8PXDD
NCI Drug Dictionary xevinapant

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
RIDADR  3077
HS Code  29339900
NFPA 704
0
2 0

AT-406(AT406) price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 19929 AT-406 ≥95% 1071992-99-8 500μg $32 2024-03-01 Buy
Cayman Chemical 19929 AT-406 ≥95% 1071992-99-8 1mg $57 2024-03-01 Buy
Cayman Chemical 19929 AT-406 ≥95% 1071992-99-8 5mg $199 2024-03-01 Buy
Cayman Chemical 19929 AT-406 ≥95% 1071992-99-8 10mg $365 2024-03-01 Buy
Medical Isotopes, Inc. 61737 SM406 1071992-99-8 1mg $610 2021-12-16 Buy
Product number Packaging Price Buy
19929 500μg $32 Buy
19929 1mg $57 Buy
19929 5mg $199 Buy
19929 10mg $365 Buy
61737 1mg $610 Buy

AT-406(AT406) Chemical Properties,Uses,Production

Description

AT-406 is an orally bioavailable Smac/DIABLO mimetic and antagonist of the inhibitor of apoptosis proteins (IAPs). It binds to XIAP, cIAP1, and cIAP2 proteins with Ki values of 66.4, 1.9, and 5.1 nM, respectively. It has been shown to inhibit cancer cell growth in various human cancer cell lines and to induce apoptosis in xenograft tumors in mice.

Uses

SM 406 is a potent and orally active antagonist of multiple inhibitor of apoptosis proteins (IAPs).

Uses

AT-406 is a potent IAP (inhibitor of apoptosis protein) inhibitor of XIAP, cIAP1, and cIAP2 with Ki of 66.4 nM, 1.9 nM, and 5.1 nM, respectively.

Biological Activity

Xevinapant (AT406, ARRY-334543, Debio1143, SM-406) is a potent Smac mimetic and an antagonist of IAP (inhibitor of apoptosis protein via E3 ubiquitin ligase), binding to XIAP-BIR3, cIAP1-BIR3 and cIAP2-BIR3 with Ki of 66.4 nM, 1.9 nM, and 5.1 nM, 50- to 100-fold higher affinities than the Smac AVPI peptide. Phase 1.

in vitro

AT-406 is a Smac mimetic and appears to mimic closely the AVPI peptide in both hydrogen bonding and hydrophobic interactions with XIAP, with additional hydrophobic contacts with W323 of XIAP. AT-406 is more sensitive to these IAPs than Smac AVPI peptide with 50-100 fold binding affinities. AT-406 (at 1 μM) completely restores the activity of caspase-9, which is suppressed by 500 nM XIAP BIR3 in a cell-free system. In MDA-MB-231 cell, AT-406 induces rapid cellular cIAP1 degradation and also pulls down the cellular XIAP protein. AT-406 effectively inhibits lots of human cancer cell lines and shows IC50 of 144 and 142 nM in MDA-MB-231 cell and SK-OV-3 ovarian cell, with low toxicity against normal-like human breast epithelial MCF-12F cells and primary human normal prostate epithelial cells. AT-406 induces apoptosis in MDA-MB-231 cell by inducing activation of caspase-3 and cleavage of PARP.

in vivo

AT-406 has good pharmacokinetic (PK) properties and oral bioavailability in mice, rats, non-human primates, and dogs. In the MDA-MB-231 xenograft, AT-406 effectively induces cIAP1 degradation and processing of procaspase-8, cleavage of PARP in tumor tissues at 100 mg/kg with well toleration even at 200 mg/kg. AT-406 induces significant tumor growth inhibition with p of 0.0012 at 100 mg/kg.

References

schimmer a d. inhibitor of apoptosis proteins: translating basic knowledge into clinical practice[j]. cancer research, 2004, 64(20): 7183-7190.cai q, sun h, peng y, et al. a potent and orally active antagonist (sm-406/at-406) of multiple inhibitor of apoptosis proteins (iaps) in clinical development for cancer treatment[j]. journal of medicinal chemistry, 2011, 54(8): 2714-2726.zhang t, li y. et al. aphysiologically based pharmacokinetic and pharmacodynamic modeling of an antagonist (sm-406/at-406) of multiple inhibitor of apoptosis proteins (iaps) in a mouse xenograft model of human breast cancer. biopharm drug dispos. 2013 sep;34(6):348-59.hurwitz hi1, smith dc, et al. safety, pharmacokinetics, and pharmacodynamic properties of oral debio1143 (at-406) in patients with advanced cancer: results of a first-in-man study. cancer chemotherpharmacol. 2015 apr;75(4):851-9.

AT-406(AT406) Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 101)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8474 58
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58

View Lastest Price from AT-406(AT406) manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
AT-406(AT406) pictures 2019-07-06 AT-406(AT406)
1071992-99-8
US $7.00 / KG 1KG 99% 100KG Career Henan Chemical Co
  • AT-406(AT406) pictures
  • AT-406(AT406)
    1071992-99-8
  • US $7.00 / KG
  • 99%
  • Career Henan Chemical Co
AT-406(AT406) (5S,8S,10aR)-N-benzhydryl-5-((S)-2-(MethylaMino)propanaMido)-3-(3-Methylbutanoyl)-6-oxodecahydropyrrolo[1,2-a][1,5]diazocine-8-carboxaMide SM 406 (5S,8S,10aR)-N-(Diphenylmethyl)decahydro-5-[[(2S)-2-(methylamino)-1-oxopropyl]amino]-3-(3-methyl-1-oxobutyl)-6-oxopyrrolo[1,2-a][1,5]diazocine-8-carboxamide AT406 (SM-406, ARRY-334543) (5S,8S,10aR)-N-(Diphenylmethyl)decahydro-5-[[(2S)-2-(methylamino)-1-oxopropyl]amino]-3-(3-methyl-1-oxobutyl)-6-oxopyrrolo[1,2-a][1,5]diazocine-8-carboxamide AT406 (SM-406, ARRY-334543) (5S,8S,10aR)-N-benzhydryl-5-((S)-2-(methylamino)propanamido)-3-(3-methylbutanoyl)-6-oxodecahyd AT-406 (SM-406) CHEMBL2158051; AT406; AT 406; SURECN2724374; QCR-136; SM406; SM 406; AT406 (SM-406) QCR-136 SureCN2724374 CHEMBL2158051 Debio-1143 SM-406;DEBIO-1143;ARRY-334543 Pyrrolo[1,2-a][1,5]diazocine-8-carboxamide, N-(diphenylmethyl)decahydro-5-[[(2S)-2-(methylamino)-1-oxopropyl]amino]-3-(3-methyl-1-oxobutyl)-6-oxo-, (5S,8S,10aR)- AT-406(Xevinapant) AT406 (Xevinapant, SM406, ARRY334543) Xevinapant SM 406,SM406,Xevinapant,AT-406,oral,inhibit,Debio 1143,ovarian,IAP,degradation,Smac,AT 406,Inhibitor,cancer,mimetic,Debio1143 Xevinapant (AT406) 1071992-99-8 C32H43N5O4 Inhibitor